Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE.
paper
Cited
Public
Unavailable
- Authors
- Lange, K; Weeks, D; Boehnke, M
- Year
- 1988
- Journal
- Genetic epidemiology
- PMID
- 3061869
- DOI
- 10.1002/gepi.1370050611
No figures extracted from this document.
No chunks — full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
Not in any collection.
No citations found.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Childhood, adolescent, and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers. | Li S et al. | — | 2025 | → |
| Age-specific breast and ovarian cancer risks associated with germline <i>BRCA1</i> or <i>BRCA2</i> pathogenic variants - an Asian study of 572 families. | Ho WK et al. | — | 2024 | → |
| Atypical cancer risk profile in carriers of Italian founder BRCA1 variant p.His1673del: Implications for classification and clinical management. | Innella G et al. | — | 2024 | → |
| Cancer Risks Associated With <i>TP53</i> Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum. | Fortuno C et al. | — | 2024 | → |
| Update of penetrance estimates in Birt-Hogg-Dubé syndrome. | Bruinsma FJ et al. | — | 2023 | → |
| Cancer Risks Associated With <i>BRCA1</i> and <i>BRCA2</i> Pathogenic Variants. | Li S et al. | — | 2022 | → |
| Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants. | Li H et al. | — | 2022 | → |
| Major Depressive Disorder and Lifestyle: Correlated Genetic Effects in Extended Twin Pedigrees. | Huider F et al. | — | 2021 | → |
| PedMiner: a tool for linkage analysis-based identification of disease-associated variants using family based whole-exome sequencing data. | Zhou J et al. | — | 2021 | → |
| Population-Based Estimates of the Age-Specific Cumulative Risk of Breast Cancer for Pathogenic Variants in <i>CHEK2</i>: Findings from the Australian Breast Cancer Family Registry. | Nguyen-Dumont T et al. | — | 2021 | → |
| TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing. | Lesueur F et al. | — | 2021 | → |
| Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study. | International Mismatch Repair Consortium | — | 2021 | → |
| Cancer Risks Associated With Germline <i>PALB2</i> Pathogenic Variants: An International Study of 524 Families. | Yang X et al. | — | 2020 | → |
| Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation? | Gemechu SD et al. | — | 2020 | → |
| Genetic and environmental causes of variation in epigenetic aging across the lifespan. | Li S et al. | — | 2020 | → |
| Inference about causation from examination of familial confounding (ICE FALCON): a model for assessing causation analogous to Mendelian randomization. | Li S et al. | — | 2020 | → |
| Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D. | Yang X et al. | — | 2020 | → |
| BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors. | Lee A et al. | — | 2019 | → |
| Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype. | Grolleman JE et al. | — | 2019 | → |
| Cancer Risks for PMS2-Associated Lynch Syndrome. | Ten Broeke SW et al. | — | 2018 | → |
| Epidemiology of ATTRV30M neuropathy in Cyprus and the modifier effect of complement C1q on the age of disease onset. | Andreou S et al. | — | 2018 | → |
| Genome-wide average DNA methylation is determined in utero. | Li S et al. | — | 2018 | → |
| Paediatric ovarian tumours and their associated cancer susceptibility syndromes. | Goudie C et al. | — | 2018 | → |
| Pedigree Selection and Information Content. | Vardarajan BN et al. | — | 2018 | → |
| The <i>BRCA1</i> c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium. | Moghadasi S et al. | — | 2018 | → |
| Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes <i>SDHB</i>, <i>SDHC</i> and <i>SDHD</i>. | Andrews KA et al. | — | 2018 | → |
| Estimating Allele Frequencies. | Adrianto I et al. | — | 2017 | → |
| Identification of Genotype Errors. | O'Connell J et al. | — | 2017 | → |
| Rules for resolving Mendelian inconsistencies in nuclear pedigrees typed for two-allele markers. | Khan SA et al. | — | 2017 | → |
| Childhood body mass index and adult mammographic density measures that predict breast cancer risk. | Hopper JL et al. | — | 2016 | → |
| Heritability of major depressive and comorbid anxiety disorders in multi-generational families at high risk for depression. | Guffanti G et al. | — | 2016 | → |
| Incorporating truncating variants in PALB2, CHEK2, and ATM into the BOADICEA breast cancer risk model. | Lee AJ et al. | — | 2016 | → |
| Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families. | Muranen TA et al. | — | 2016 | → |
| Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH. | Win AK et al. | — | 2016 | → |
| A risk prediction algorithm for ovarian cancer incorporating BRCA1, BRCA2, common alleles and other familial effects. | Jervis S et al. | — | 2015 | → |
| Bias Correction Methods Explain Much of the Variation Seen in Breast Cancer Risks of BRCA1/2 Mutation Carriers. | Vos JR et al. | — | 2015 | → |
| Breast cancer risk for Korean women with germline mutations in BRCA1 and BRCA2. | Park B et al. | — | 2015 | → |
| Changes in Zinc Transporter 8 Autoantibodies Following Type 1 Diabetes Onset: The Type 1 Diabetes Genetics Consortium Autoantibody Workshop. | Wenzlau JM et al. | — | 2015 | → |
| Genetic and epigenetic trends in telomere research: a novel way in immunoepigenetics. | Melicher D et al. | — | 2015 | → |
| Genetic linkage analysis in the age of whole-genome sequencing. | Ott J et al. | — | 2015 | → |
| Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21. | Fernandez-Navarro P et al. | — | 2015 | → |
| Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer. | Ramus SJ et al. | — | 2015 | → |
| Lynch syndrome and cervical cancer. | Antill YC et al. | — | 2015 | → |
| Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome. | Guindalini RS et al. | — | 2015 | → |
| Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers. | Kuchenbaecker KB et al. | — | 2014 | → |
| Attenuated familial adenomatous polyposis manifests as autosomal dominant late-onset colorectal cancer. | Ibrahim A et al. | — | 2014 | → |
| BOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interface. | Lee AJ et al. | — | 2014 | → |
| Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations. | Brohet RM et al. | — | 2014 | → |
| Breast-cancer risk in families with mutations in PALB2. | Antoniou AC et al. | — | 2014 | → |
| Estimating risks for variants of unknown significance according to their predicted pathogenicity classes with application to BRCA1. | Dowty JG et al. | — | 2014 | → |
| Mega2: validated data-reformatting for linkage and association analyses. | Baron RV et al. | — | 2014 | → |
| Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers. | Park DJ et al. | — | 2014 | → |
| Architecture of cortical bone determines in part its remodelling and structural decay. | Bui M et al. | — | 2013 | → |
| A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees. | Silberstein M et al. | — | 2013 | → |
| Cancer risks for MLH1 and MSH2 mutation carriers. | Dowty JG et al. | — | 2013 | → |
| Dosage transmission disequilibrium test (dTDT) for linkage and association detection. | Zhang Z et al. | — | 2013 | → |
| Elevated risk of prostate cancer among men with Lynch syndrome. | Raymond VM et al. | — | 2013 | → |
| Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer. | Barnes DR et al. | — | 2013 | → |
| Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. | Couch FJ et al. | — | 2013 | → |
| Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk. | Gaudet MM et al. | — | 2013 | → |
| Mendel: the Swiss army knife of genetic analysis programs. | Lange K et al. | — | 2013 | → |
| Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer. | Ruark E et al. | — | 2013 | → |
| Population-based estimate of prostate cancer risk for carriers of the HOXB13 missense mutation G84E. | MacInnis RJ et al. | — | 2013 | → |
| A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels. | Froguel P et al. | — | 2012 | → |
| A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers. | Ding YC et al. | — | 2012 | → |
| Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. | Antoniou AC et al. | — | 2012 | → |
| Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers. | Maia AT et al. | — | 2012 | → |
| Estimating allele frequencies. | Adrianto I et al. | — | 2012 | → |
| Evaluation of association methods for analysing modifiers of disease risk in carriers of high-risk mutations. | Barnes DR et al. | — | 2012 | → |
| Identification of genotype errors. | Shugart YY et al. | — | 2012 | → |
| Model-free tests for genetic linkage. | Amos CI et al. | — | 2012 | → |
| Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers. | Ramus SJ et al. | — | 2012 | → |
| Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering. | Markello TC et al. | — | 2012 | → |
| The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers. | Laitman Y et al. | — | 2012 | → |
| A risk prediction algorithm based on family history and common genetic variants: application to prostate cancer with potential clinical impact. | Macinnis RJ et al. | — | 2011 | → |
| Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer. | Win AK et al. | — | 2011 | → |
| Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers. | Antoniou AC et al. | — | 2011 | → |
| Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2. | Mulligan AM et al. | — | 2011 | → |
| Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes. | van Vliet CM et al. | — | 2011 | → |
| Enhanced genetic maps from family-based disease studies: population-specific comparisons. | He C et al. | — | 2011 | → |
| Family-based designs for genome-wide association studies. | Ott J et al. | — | 2011 | → |
| Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. | Ramus SJ et al. | — | 2011 | → |
| Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. | Zlojutro M et al. | — | 2011 | → |
| Germline mutations in RAD51D confer susceptibility to ovarian cancer. | Loveday C et al. | — | 2011 | → |
| High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation. | Mukherjee B et al. | — | 2011 | → |
| Rare variants in the ATM gene and risk of breast cancer. | Goldgar DE et al. | — | 2011 | → |
| Stability selection for genome-wide association. | Alexander DH et al. | — | 2011 | → |
| A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. | Antoniou AC et al. | — | 2010 | → |
| A PALB2 mutation associated with high risk of breast cancer. | Southey MC et al. | — | 2010 | → |
| Are we overestimating the penetrance of mutations in SDHB? | Schiavi F et al. | — | 2010 | → |
| Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction. | Antoniou AC et al. | — | 2010 | → |
| Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. | Gaudet MM et al. | — | 2010 | → |
| Contrasting methods of quantifying fine structure of human recombination. | Clark AG et al. | — | 2010 | → |
| Incorporating tumour pathology information into breast cancer risk prediction algorithms. | Mavaddat N et al. | — | 2010 | → |
| Metabolic syndrome-related composite factors over 5 years in the STANISLAS family study: genetic heritability and common environmental influences. | Herbeth B et al. | — | 2010 | → |
| MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families. | Borràs E et al. | — | 2010 | → |
| Prostate cancer segregation analyses using 4390 families from UK and Australian population-based studies. | MacInnis RJ et al. | — | 2010 | → |
| The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers. | Jakubowska A et al. | — | 2010 | → |
| Variant in the 3' region of the IkappaBalpha gene associated with insulin resistance in Hispanic Americans: The IRAS Family Study. | Miller MR et al. | — | 2010 | → |
| Bayesian latent trait modeling of migraine symptom data. | Chen CC et al. | — | 2009 | → |
| Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome. | Stoffel E et al. | — | 2009 | → |
| Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry. | Pal P et al. | — | 2009 | → |
| Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. | Antoniou AC et al. | — | 2009 | → |
| Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis. | Zinovieva E et al. | — | 2009 | → |
| Estimating fetal and maternal genetic contributions to premature birth from multiparous pregnancy histories of twins using MCMC and maximum-likelihood approaches. | York TP et al. | — | 2009 | → |
| Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). | Osorio A et al. | — | 2009 | → |
| Genetic models for the familial aggregation of mammographic breast density. | Kataoka M et al. | — | 2009 | → |
| Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. | Falchi M et al. | — | 2009 | → |
| Genotype imputation. | Li Y et al. | — | 2009 | → |
| Linkage analysis of schizophrenia controlling for population substructure. | Paunio T et al. | — | 2009 | → |
| Linkage and heritability analysis of migraine symptom groupings: a comparison of three different clustering methods on twin data. | Chen CC et al. | — | 2009 | → |
| No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study. | Rebbeck TR et al. | — | 2009 | → |
| Risk of pancreatic cancer in families with Lynch syndrome. | Kastrinos F et al. | — | 2009 | → |
| Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. | Benyamin B et al. | — | 2009 | → |
| A reanalysis of 409 European-Ancestry and African American schizophrenia pedigrees reveals significant linkage to 8p23.3 with evidence of locus heterogeneity. | Holliday EG et al. | — | 2008 | → |
| Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. | Antoniou AC et al. | — | 2008 | → |
| Contribution of genes and environment to variation in postural changes in mean arterial and pulse pressure. | Scurrah KJ et al. | — | 2008 | → |
| Frequencies of polymorphisms associated with BSE resistance differ significantly between Bos taurus, Bos indicus, and composite cattle. | Brunelle BW et al. | — | 2008 | → |
| Penetrance analysis of the PALB2 c.1592delT founder mutation. | Erkko H et al. | — | 2008 | → |
| Relationship uncertainty linkage statistics (RULS): affected relative pair statistics that model relationship uncertainty. | Ray A et al. | — | 2008 | → |
| Short communication: Allele, genotype, and haplotype data for bovine spongiform encephalopathy-resistance polymorphisms from healthy US Holstein cattle. | Brunelle BW et al. | — | 2008 | → |
| The average cumulative risks of breast and ovarian cancer for carriers of mutations in BRCA1 and BRCA2 attending genetic counseling units in Spain. | Milne RL et al. | — | 2008 | → |
| The RAD51D E233G variant and breast cancer risk: population-based and clinic-based family studies of Australian women. | Dowty JG et al. | — | 2008 | → |
| Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian population. | Ellis JA et al. | — | 2007 | → |
| Error detection in SNP data by considering the likelihood of recombinational history implied by three-site combinations. | Toleno DM et al. | — | 2007 | → |
| Evaluation of mathematical models for breast cancer risk assessment in routine clinical use. | Fasching PA et al. | — | 2007 | → |
| Genetic and environmental determinants of circulating resistin level in a community-based sample. | Pantsulaia I et al. | — | 2007 | → |
| Hand bone midshaft enthesophytes: the influence of age, sex, and heritability. | Kalichman L et al. | — | 2007 | → |
| Heritability and segregation analysis of osteosarcoma in the Scottish deerhound. | Phillips JC et al. | — | 2007 | → |
| Heritability of serum hs-CRP concentration and 5-year changes in the Stanislas family study: association with apolipoprotein E alleles. | Berrahmoune H et al. | — | 2007 | → |
| RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. | Antoniou AC et al. | — | 2007 | → |
| Separation of base allele and sampling term effects gives new insights in variance component QTL analysis. | Rönnegård L et al. | — | 2007 | → |
| Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin. | Pal P et al. | — | 2007 | → |
| The elusive goal of pedigree weights. | Sengul H et al. | — | 2007 | → |
| A genome wide linkage search for breast cancer susceptibility genes. | Smith P et al. | — | 2006 | → |
| A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers. | Thompson D et al. | — | 2006 | → |
| A possible smoking susceptibility locus on chromosome 11p12: evidence from sex-limitation linkage analyses in a sample of Australian twin families. | Morley KI et al. | — | 2006 | → |
| BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families. | Antoniou AC et al. | — | 2006 | → |
| BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives. | Lalloo F et al. | — | 2006 | → |
| Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling. | Waddell N et al. | — | 2006 | → |
| Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34. | Herzberg I et al. | — | 2006 | → |
| Evidence for a gene influencing high-density lipoprotein cholesterol on chromosome 4q31.21. | Dastani Z et al. | — | 2006 | → |
| Genetic and environmental determinants of circulating levels of angiogenin in community-based sample. | Pantsulaia Ia et al. | — | 2006 | → |
| Genetic and environmental determinants of variation of soluble adhesion molecules. | Vistoropsky Y et al. | — | 2006 | → |
| Genetic and environmental influences on variation in balance performance among female twin pairs aged 21-82 years. | El Haber N et al. | — | 2006 | → |
| Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants. | Lovelock PK et al. | — | 2006 | → |
| Genome-wide linkage scan for loci influencing plasma triglycerides. | Middelberg RP et al. | — | 2006 | → |
| Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample. | Suarez BK et al. | — | 2006 | → |
| Modelling germline mosaicism and different new mutation rates simultaneously for appropriate risk calculations in families with Duchenne muscular dystrophy. | Fischer C et al. | — | 2006 | → |
| Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees. | Wijsman EM et al. | — | 2006 | → |
| Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the Breast Cancer Family Registry. | Bernstein JL et al. | — | 2006 | → |
| RISCALW: a Windows program for risk calculation in families with Duchenne muscular dystrophy. | Fischer C et al. | — | 2006 | → |
| Risk prediction models for familial breast cancer. | Antoniou AC et al. | — | 2006 | → |
| Sex differences in genetic and environmental determinants of pulse pressure. | Scurrah KJ et al. | — | 2006 | → |
| Variants in the HEPSIN gene are associated with prostate cancer in men of European origin. | Pal P et al. | — | 2006 | → |
| Variation in femoral length is associated with polymorphisms in RUNX2 gene. | Ermakov S et al. | — | 2006 | → |
| A protein-truncating mutation in CYP17A1 in three sisters with early-onset breast cancer. | Hopper JL et al. | — | 2005 | → |
| Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha population. | Suk EK et al. | — | 2005 | → |
| Association of leptin levels with obesity and blood pressure: possible common genetic variation. | Livshits G et al. | — | 2005 | → |
| Association testing with Mendel. | Lange K et al. | — | 2005 | → |
| Cancer risks and mortality in heterozygous ATM mutation carriers. | Thompson D et al. | — | 2005 | → |
| Contribution of BRCA1 and BRCA2 germ-line mutations to the incidence of breast cancer in young women: results from a prospective population-based study in France. | Bonadona V et al. | — | 2005 | → |
| Contribution of the familial and genetic factors on monocyte chemoattractant protein-1 variation in healthy human pedigrees. | Pantsulaia I et al. | — | 2005 | → |
| Determinants of variation in serum paraoxonase enzyme activity in baboons. | Rainwater DL et al. | — | 2005 | → |
| Fishing for pleiotropic QTLs in a polygenic sea. | Bauman LE et al. | — | 2005 | → |
| Genetic regulation of the variation of circulating insulin-like growth factors and leptin in human pedigrees. | Pantsulaia I et al. | — | 2005 | → |
| Genome-wide scan for myopia in the Old Order Amish. | Stambolian D et al. | — | 2005 | → |
| Genomewide significant linkage to migrainous headache on chromosome 5q21. | Nyholt DR et al. | — | 2005 | → |
| GMCheck: Bayesian error checking for pedigree genotypes and phenotypes. | Thomas A | — | 2005 | → |
| Linkage analysis of plasma ApoE in three ethnic groups: multiple genes with context-dependent effects. | Klos KL et al. | — | 2005 | → |
| Maximum likelihood haplotyping for general pedigrees. | Fishelson M et al. | — | 2005 | → |
| Mega2: data-handling for facilitating genetic linkage and association analyses. | Mukhopadhyay N et al. | — | 2005 | → |
| PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data. | Wigginton JE et al. | — | 2005 | → |
| Quantitative genetic study of head size related phenotypes in ethnically homogeneous Chuvasha pedigrees. | Ermakov S et al. | — | 2005 | → |
| Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment. | Quehenberger F et al. | — | 2005 | → |
| Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families. | Cornes BK et al. | — | 2005 | → |
| SNP haplotypes in the angiotensin I-converting enzyme (ACE) gene: analysis of Nigerian family data using gamete competition models. | McKenzie CA et al. | — | 2005 | → |
| Software for quantitative trait analysis. | Almasy L et al. | — | 2005 | → |
| Spouse selection and environmental effects on spouse correlation in lung function measures. | Knuiman MW et al. | — | 2005 | → |
| TGFBR1*6A is not associated with prostate cancer in men of European ancestry. | Suarez BK et al. | — | 2005 | → |
| A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10. | Shimizu S et al. | — | 2004 | → |
| Analysis of candidate genes for prostate cancer. | Burmester JK et al. | — | 2004 | → |
| A quantitative trait locus influences coordinated variation in measures of ApoB-containing lipoproteins. | Rainwater DL et al. | — | 2004 | → |
| Best linear unbiased allele-frequency estimation in complex pedigrees. | McPeek MS et al. | — | 2004 | → |
| Breast cancer genetics: unsolved questions and open perspectives in an expanding clinical practice. | Hodgson SV et al. | — | 2004 | → |
| Familial and genomic analyses of postural changes in systolic and diastolic blood pressure. | Harrap SB et al. | — | 2004 | → |
| Genetic influences on the circulating cytokines involved in osteoclastogenesis. | Livshits G et al. | — | 2004 | → |
| Genome-wide linkage of forced mid-expiratory flow in chronic obstructive pulmonary disease. | DeMeo DL et al. | — | 2004 | → |
| Heritability of circulating growth factors involved in the angiogenesis in healthy human population. | Pantsulaia I et al. | — | 2004 | → |
| Heritability of left ventricular dimensions and mass in American Indians: The Strong Heart Study. | Bella JN et al. | — | 2004 | → |
| Increased power for case-control studies of single nucleotide polymorphisms through incorporation of family history and genetic constraints. | Thompson D et al. | — | 2004 | → |
| Polyglutamine repeat length in the AIB1 gene modifies breast cancer susceptibility in BRCA1 carriers. | Kadouri L et al. | — | 2004 | → |
| The BOADICEA model of genetic susceptibility to breast and ovarian cancer. | Antoniou AC et al. | — | 2004 | → |
| Whole genome scan for obstructive sleep apnea and obesity in African-American families. | Palmer LJ et al. | — | 2004 | → |
| A full-likelihood method for the evaluation of causality of sequence variants from family data. | Thompson D et al. | — | 2003 | → |
| A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions. | Seddon JM et al. | — | 2003 | → |
| A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21. | Boyadjiev SA et al. | — | 2003 | → |
| Antihypertensive treatments obscure familial contributions to blood pressure variation. | Cui JS et al. | — | 2003 | → |
| Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. | Antoniou A et al. | — | 2003 | → |
| A whole-genome scan for obstructive sleep apnea and obesity. | Palmer LJ et al. | — | 2003 | → |
| Bivariate variance-component analysis, with application to systolic blood pressure and total cholesterol levels in the Framingham Heart Study. | Cui JS et al. | — | 2003 | → |
| Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy. | Moroi SE et al. | — | 2003 | → |
| Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland. | Auranen M et al. | — | 2003 | → |
| Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus. | Justice CM et al. | — | 2003 | → |
| Genetic diversity and background linkage disequilibrium in the North American Holstein cattle population. | Vallejo RL et al. | — | 2003 | → |
| Genetic variation of circulating leptin is involved in genetic variation of hand bone size and geometry. | Livshits G et al. | — | 2003 | → |
| Linkage analysis of adult height with parent-of-origin effects in the Framingham Heart Study. | Mukhopadhyay N et al. | — | 2003 | → |
| Localization of genes that control LDL size fractions in baboons. | Rainwater DL et al. | — | 2003 | → |
| Multivariate variance-components analysis of longitudinal blood pressure measurements from the Framingham Heart Study. | Kraft P et al. | — | 2003 | → |
| Polygenic inheritance of breast cancer: Implications for design of association studies. | Antoniou AC et al. | — | 2003 | → |
| Polymorphisms in the nephrin gene and diabetic nephropathy in type 1 diabetic patients. | Pettersson-Fernholm K et al. | — | 2003 | → |
| Quantitative genetic study of radiographic hand bone size and geometry. | Livshits G et al. | — | 2003 | → |
| Regressive logistic and proportional hazards disease models for within-family analyses of measured genotypes, with application to a CYP17 polymorphism and breast cancer. | Cui JS et al. | — | 2003 | → |
| Re: On the use of familial aggregation in population-based case probands for calculating penetrance. | Amos CI | — | 2003 | → |
| Significant linkage of Parkinson disease to chromosome 2q36-37. | Pankratz N et al. | — | 2003 | → |
| The effect of disease penetrance, family size, and age of onset on family history with application to setting eligibility criteria for genetic testing. | Sibert A et al. | — | 2003 | → |
| The functional -374 T/A RAGE gene polymorphism is associated with proteinuria and cardiovascular disease in type 1 diabetic patients. | Pettersson-Fernholm K et al. | — | 2003 | → |
| The future of association studies of common cancers. | Houlston RS et al. | — | 2003 | → |
| A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes. | Antoniou AC et al. | — | 2002 | → |
| A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. | Auranen M et al. | — | 2002 | → |
| Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. | Van Eerdewegh P et al. | — | 2002 | → |
| Codon and rate variation models in molecular phylogeny. | Schadt E et al. | — | 2002 | → |
| Combined segregation and linkage analysis of HLA markers in familial psoriasis. | Guo SW et al. | — | 2002 | → |
| Detection and integration of genotyping errors in statistical genetics. | Sobel E et al. | — | 2002 | → |
| Determining Complex Genetic Risks by Computer. | Flodman P et al. | — | 2002 | → |
| Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysis. | Steinle NI et al. | — | 2002 | → |
| Family resemblance in breakfast energy intake: the Stanislas Family Study. | Billon S et al. | — | 2002 | → |
| Genes and family environment explain correlations between blood pressure and body mass index. | Cui J et al. | — | 2002 | → |
| Genetic and environmental influences on IL-6 and TNF-alpha plasma levels in apparently healthy general population. | Pantsulaia I et al. | — | 2002 | → |
| Genetic influences on aortic root size in American Indians: the Strong Heart Study . | Bella JN et al. | — | 2002 | → |
| Genetic variability of adult body mass index: a longitudinal assessment in framingham families. | Coady SA et al. | — | 2002 | → |
| Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease. | Silverman EK et al. | — | 2002 | → |
| Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes. | Straub RE et al. | — | 2002 | → |
| Locus controlling LDL cholesterol response to dietary cholesterol is on baboon homologue of human chromosome 6. | Kammerer CM et al. | — | 2002 | → |
| Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. | Meijers-Heijboer H et al. | — | 2002 | → |
| Palmar hyperhidrosis: evidence of genetic transmission. | Ro KM et al. | — | 2002 | → |
| Single-sperm typing. | Lien S et al. | — | 2002 | → |
| Statistics for nonparametric linkage analysis of X-linked traits in general pedigrees. | Song KK et al. | — | 2002 | → |
| X-linked recessive atrophic macular degeneration from RPGR mutation. | Ayyagari R et al. | — | 2002 | → |
| A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion. | Margolis RL et al. | — | 2001 | → |
| A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion. | Margolis RL et al. | — | 2001 | → |
| After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer. | Cui J et al. | — | 2001 | → |
| A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22. | Kelsoe JR et al. | — | 2001 | → |
| A survey of affected-sibship statistics for nonparametric linkage analysis. | Sengul H et al. | — | 2001 | → |
| A train of thoughts on gene mapping. | Hoh J et al. | — | 2001 | → |
| Detecting population outliers and null alleles in linkage data: application to GAW12 asthma studies. | Fisher SA et al. | — | 2001 | → |
| Estimation of allele frequencies with data on sibships. | Broman KW | — | 2001 | → |
| Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study. | Antoniou AC et al. | — | 2001 | → |
| Familial resemblance of body composition in prepubertal girls and their biological parents. | Treuth MS et al. | — | 2001 | → |
| Genetic epidemiology of fecal egg excretion during Schistosoma mansoni infection in an endemic area in Minas Gerais, Brazil. | Bethony J et al. | — | 2001 | → |
| Homozygosity mapping using pooled DNA. | Sheffield VC | — | 2001 | → |
| Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families. | Pharoah PD et al. | — | 2001 | → |
| Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups. | Perola M et al. | — | 2001 | → |
| Segregation analyses of 1,476 population-based Australian families affected by prostate cancer. | Cui J et al. | — | 2001 | → |
| Sodium-lithium countertransport activity is linked to chromosome 5 in baboons. | Kammerer CM et al. | — | 2001 | → |
| Using step-wise linear regression to detect "functional" sequence variants: application to simulated data. | Mitchell BD et al. | — | 2001 | → |
| Variation in cancer risks, by mutation position, in BRCA2 mutation carriers. | Thompson D et al. | — | 2001 | → |
| Assessment of different sources of variation in the antibody responses to specific malaria antigens in children in Papua New Guinea. | Stirnadel HA et al. | — | 2000 | → |
| Birth weight and the metabolic syndrome: thrifty phenotype or thrifty genotype? | Stern MP et al. | — | 2000 | → |
| Bootstrap confidence intervals for relative risk parameters in affected-sib-pair data. | Cordell HJ et al. | — | 2000 | → |
| Clinical and genetic analysis of a large North European Caucasian family affected by early-onset periodontitis. | Hodge PJ et al. | — | 2000 | → |
| Gamete-competition models. | Sinsheimer JS et al. | — | 2000 | → |
| Genetic analysis of growth curve parameters of body weight, height and head circumference. | Livshits G et al. | — | 2000 | → |
| Major genes regulating total serum immunoglobulin E levels in families with asthma. | Xu J et al. | — | 2000 | → |
| Quantitative genetic analysis of circulating levels of biochemical markers of bone formation. | Livshits G et al. | — | 2000 | → |
| Risk models for familial ovarian and breast cancer. | Antoniou AC et al. | — | 2000 | → |
| Statistical approaches to gene mapping. | Ott J et al. | — | 2000 | → |
| The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes. | Ghosh S et al. | — | 2000 | → |
| The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci. | Watanabe RM et al. | — | 2000 | → |
| The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia. | Hoffer MJ et al. | — | 2000 | → |
| Urinary albumin excretion in families with type 2 diabetes is heritable and genetically correlated to blood pressure. | Fogarty DG et al. | — | 2000 | → |
| Cancer risks in BRCA2 mutation carriers. | Breast Cancer Linkage Consortium | — | 1999 | → |
| Comparison of variance components and sibpair-based approaches to quantitative trait linkage analysis in unselected samples. | Williams JT et al. | — | 1999 | → |
| Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome. | Ying L et al. | — | 1999 | → |
| Effects of genotype x sex interaction on linkage analysis of visual event-related evoked potentials. | Towne B et al. | — | 1999 | → |
| Estimation of nonpaternity in the Mexican population of Nuevo Leon: a validation study with blood group markers. | Cerda-Flores RM et al. | — | 1999 | → |
| Genetic analysis of motor milestones attainment in early childhood. | Peter I et al. | — | 1999 | → |
| Genetic variance components analysis for binary phenotypes using generalized linear mixed models (GLMMs) and Gibbs sampling. | Burton PR et al. | — | 1999 | → |
| Heritability and segregation analysis of immune responses to specific malaria antigens in Papua New Guinea. | Stirnadel HA et al. | — | 1999 | → |
| Inherited susceptibility to bleomycin-induced chromatid breaks in cultured peripheral blood lymphocytes. | Cloos J et al. | — | 1999 | → |
| Linkage analysis and loss of heterozygosity for chromosome arm 1p in familial breast cancer. | Millikan RC et al. | — | 1999 | → |
| Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11. | Richter A et al. | — | 1999 | → |
| Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions. | Lopez Correa C et al. | — | 1999 | → |
| Percent of oxygen saturation of arterial hemoglobin among Bolivian Aymara at 3,900-4,000 m. | Beall CM et al. | — | 1999 | → |
| The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes. | Gayther SA et al. | — | 1999 | → |
| Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. | Ghosh S et al. | — | 1999 | → |
| A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping. | Haider NB et al. | — | 1998 | → |
| A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. | Ginns EI et al. | — | 1998 | → |
| A large sample of finnish diabetic sib-pairs reveals no evidence for a non-insulin-dependent diabetes mellitus susceptibility locus at 2qter. | Ghosh S et al. | — | 1998 | → |
| A schizophrenia locus may be located in region 10p15-p11. | Straub RE et al. | — | 1998 | → |
| Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11. | Othman MI et al. | — | 1998 | → |
| Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia. | Hoffer MJ et al. | — | 1998 | → |
| Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3. | Brown GM et al. | — | 1998 | → |
| Multipoint quantitative-trait linkage analysis in general pedigrees. | Almasy L et al. | — | 1998 | → |
| PedCheck: a program for identification of genotype incompatibilities in linkage analysis. | O'Connell JR et al. | — | 1998 | → |
| Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster County. | Agarwala R et al. | — | 1998 | → |
| A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2. | Comuzzie AG et al. | — | 1997 | → |
| Beyond one gene-one disease: alternative strategies for deciphering genetic determinants of osteoporosis. | Rogers J et al. | — | 1997 | → |
| Bivariate quantitative trait linkage analysis: pleiotropy versus co-incident linkages. | Almasy L et al. | — | 1997 | → |
| Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13. | Easton DF et al. | — | 1997 | → |
| Comparison of sib-pair and variance-components methods for genomic screening. | Pugh EW et al. | — | 1997 | → |
| Cosegregation of open-angle glaucoma and the nail-patella syndrome. | Lichter PR et al. | — | 1997 | → |
| Effects of genotype-by-sex interaction on quantitative trait linkage analysis. | Towne B et al. | — | 1997 | → |
| Genetic contribution of the endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels. | Wang XL et al. | — | 1997 | → |
| Genetic effects on variation in red-blood-cell folate in adults: implications for the familial aggregation of neural tube defects. | Mitchell LE et al. | — | 1997 | → |
| Genetic factors associated with altered sodium transport in human hypertension: a twin study. | Nowson CA et al. | — | 1997 | → |
| Genetic influence on cytokine production and fatal meningococcal disease. | Westendorp RG et al. | — | 1997 | → |
| Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. | Edenberg HJ et al. | — | 1997 | → |
| Is fragile X syndrome a risk factor for dizygotic twinning? | Healey SC et al. | — | 1997 | → |
| Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group. | Ghosh S et al. | — | 1997 | → |
| Multipoint oligogenic linkage analysis of quantitative traits. | Blangero J et al. | — | 1997 | → |
| Nonsense mutation in exon 3 of the proteolipid protein gene (PLP) in a family with an unusual form of Pelizaeus-Merzbacher disease. | Hodes ME et al. | — | 1997 | → |
| Power of variance component linkage analysis to detect epistasis. | Mitchell BD et al. | — | 1997 | → |
| Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. | Cooney KA et al. | — | 1997 | → |
| Statistical Modeling Approaches to Genetic Analysis. | Dyke B et al. | — | 1997 | → |
| Statistical properties of a variance components method for quantitative trait linkage analysis in nuclear families and extended pedigrees. | Williams JT et al. | — | 1997 | → |
| The age dependency of gene expression for plasma lipids, lipoproteins, and apolipoproteins. | Snieder H et al. | — | 1997 | → |
| Ventilation and hypoxic ventilatory response of Tibetan and Aymara high altitude natives. | Beall CM et al. | — | 1997 | → |
| Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. | — | — | 1996 | → |
| An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds. | Scott DA et al. | — | 1996 | → |
| Clinical phenotype of juvenile-onset primary open-angle glaucoma linked to chromosome 1q. | Johnson AT et al. | — | 1996 | → |
| Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. | Sobel E et al. | — | 1996 | → |
| Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families. | Kendler KS et al. | — | 1996 | → |
| Evidence for linkage of regions on chromosomes 6 and 11 to plasma glucose concentrations in Mexican Americans. | Stern MP et al. | — | 1996 | → |
| Familial correlations, cohabitation effects, and heritability for cardiovascular risk factors. | Knuiman MW et al. | — | 1996 | → |
| Genetic and environmental contributions to cardiovascular risk factors in Mexican Americans. The San Antonio Family Heart Study. | Mitchell BD et al. | — | 1996 | → |
| Genetic basis of variation in carotid artery wall thickness. | Duggirala R et al. | — | 1996 | → |
| Genetic heterogeneity in hereditary breast cancer: role of BRCA1 and BRCA2. | Rebbeck TR et al. | — | 1996 | → |
| Identifying marker typing incompatibilities in linkage analysis. | Stringham HM et al. | — | 1996 | → |
| Irish study on high-density schizophrenia families: field methods and power to detect linkage. | Kendler KS et al. | — | 1996 | → |
| Juvenile glaucoma linked to GLCIA in a Panamanian family. | Lichter PR et al. | — | 1996 | → |
| Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification. | Sheffield VC et al. | — | 1996 | → |
| Polymorphism at the ovine major histocompatibility complex class II loci. | Escayg AP et al. | — | 1996 | → |
| Probable exclusion of GLC1A as a candidate glaucoma gene in a family with middle-age-onset primary open-angle glaucoma. | Richards JE et al. | — | 1996 | → |
| Programs, databases, and expert systems for human geneticists--a survey. | Fischer C et al. | — | 1996 | → |
| Quantitative variation in obesity-related traits and insulin precursors linked to the OB gene region on human chromosome 7. | Duggirala R et al. | — | 1996 | → |
| Software for genetic linkage analysis: an update. | Bryant SP | — | 1996 | → |
| The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia. | Hoffer MJ et al. | — | 1996 | → |
| A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity. | Straub RE et al. | — | 1995 | → |
| Approximate solutions for the maximum-likelihood estimates in models of univariate human twin data. | Wijesiri UW et al. | — | 1995 | → |
| Computer programs for multilocus haplotyping of general pedigrees. | Weeks DE et al. | — | 1995 | → |
| Effects of age, sex, and heredity on measures of bone mass in baboons (Papio hamadryas). | Kammerer CM et al. | — | 1995 | → |
| Effects of sex, age, weight, and heredity on blood pressure in baboons. | Kammerer CM | — | 1995 | → |
| Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22. | Wang S et al. | — | 1995 | → |
| Growth in stature in fragile X families: a mixed longitudinal study. | Loesch DZ et al. | — | 1995 | → |
| Heritability of age at first birth in captive olive baboons. | Williams-Blangero S et al. | — | 1995 | → |
| HLA disease associations: models for the study of complex human genetic disorders. | Thomson G | — | 1995 | → |
| Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7. | Rowe RE et al. | — | 1995 | → |
| Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus. | Wapelhorst B et al. | — | 1995 | → |
| Linkage of LHB and MAG to GPI on sheep chromosome 14. | Penty JM et al. | — | 1995 | → |
| New localization of NCAM, proximal to DRD2 at chromosome 11q23. | Telatar M et al. | — | 1995 | → |
| Pelizaeus-Merzbacher disease caused by a de novo mutation that originated in exon 2 of the maternal great-grandfather of the propositus. | Pratt VM et al. | — | 1995 | → |
| Sheep linkage mapping: RFLP markers for comparative mapping studies. | Montgomery GW et al. | — | 1995 | → |
| Timing and genetic rapport between growth in skeletal maturity and height around puberty: similarities and differences between girls and boys. | Loesch DZ et al. | — | 1995 | → |
| A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34. | McDonald MT et al. | — | 1994 | → |
| Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map. | Matise TC et al. | — | 1994 | → |
| Detection of tandem duplications and implications for linkage analysis. | Matise TC et al. | — | 1994 | → |
| Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2. | Pulver AE et al. | — | 1994 | → |
| Genetic determination of telomere size in humans: a twin study of three age groups. | Slagboom PE et al. | — | 1994 | → |
| Genetic epidemiology of early onset breast cancer. | Eccles D et al. | — | 1994 | → |
| Genetic modulation of telomeric terminal restriction-fragment length: relevance for clonal aging and late-life disease. | Martin GM | — | 1994 | → |
| LABMAN and LINKMAN: a data management system specifically designed for genome searches of complex diseases. | Adams P | — | 1994 | → |
| Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome Iq. | Richards JE et al. | — | 1994 | → |
| Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? | Schmitt K et al. | — | 1994 | → |
| Multipoint mapping calculations for sperm-typing data. | Lazzeroni LC et al. | — | 1994 | → |
| Possible localization of a major gene for cleft lip and palate to 4q. | Beiraghi S et al. | — | 1994 | → |
| Sources of variability of human plasma apolipoprotein A-IV levels and relationships with lipid metabolism. | Zaiou M et al. | — | 1994 | → |
| The effect of variation in the apolipoprotein B gene on plasmid lipid and apolipoprotein B levels. I. A likelihood-based approach to cladistic analysis. | Hallman DM et al. | — | 1994 | → |
| Transmitting males and carrier females in fragile X--revisited. | Loesch DZ et al. | — | 1994 | → |
| Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers. | de Knijff P et al. | — | 1994 | → |
| A DNA polymorphism for lecithin:cholesterol acyltransferase (LCAT) is associated with high density lipoprotein cholesterol concentrations in baboons. | Kammerer CM et al. | — | 1993 | → |
| Analyzing twin resemblance in multisymptom data: genetic applications of a latent class model for symptoms of conduct disorder in juvenile boys. | Eaves LJ et al. | — | 1993 | → |
| An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genes. | Easton DF et al. | — | 1993 | → |
| BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis. | Chamberlain JS et al. | — | 1993 | → |
| Detecting heterogeneity with the affected-pedigree-member (APM) method. | Matise TC et al. | — | 1993 | → |
| Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees. | Baron M et al. | — | 1993 | → |
| Effect of fragile X on physical and intellectual traits estimated by pedigree analysis. | Loesch DZ et al. | — | 1993 | → |
| Effect of the fragile X anomaly on body proportions estimated by pedigree analysis. | Loesch DZ et al. | — | 1993 | → |
| Genotype by sex interaction in measures of lipids, lipoproteins, and apolipoproteins. | Towne B et al. | — | 1993 | → |
| Genotype-phenotype relationships in fragile X syndrome: a family study. | Loesch DZ et al. | — | 1993 | → |
| Levels of anti-pneumococcal antibodies in young children in Papua New Guinea. | Pomat WS et al. | — | 1993 | → |
| Linkage between complement components 6 and 7 and glutamic pyruvate transaminase in the marsupial Monodelphis domestica. | van Oorschot RA et al. | — | 1993 | → |
| Linkage of a major breast cancer gene to chromosome 17q12-21: results from 15 Edinburgh families. | Cohen BB et al. | — | 1993 | → |
| Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred. | Pratt VM et al. | — | 1993 | → |
| Lipid data from NHLBI veteran twins: interpreting genetic analyses when model assumptions fail. | Williams CJ et al. | — | 1993 | → |
| Match probabilities in racially admixed populations. | Lange K | — | 1993 | → |
| Metropolis sampling in pedigree analysis. | Sobel E et al. | — | 1993 | → |
| Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy. | Mutirangura A et al. | — | 1993 | → |
| Polymorphisms in the Tcrb-V2 gene segments localize the Tcrb orphon genes to human chromosome 9p21. | Charmley P et al. | — | 1993 | → |
| Quantitative genetics of sexual dimorphism in body fat measurements. | Comuzzie AG et al. | — | 1993 | → |
| Reevaluation of the chromosome 4q candidate region for early onset periodontitis. | Hart TC et al. | — | 1993 | → |
| Selective breeding to develop lines of baboons with high and low blood pressure. | Carey D et al. | — | 1993 | → |
| The ovine Booroola fecundity gene (FecB) is linked to markers from a region of human chromosome 4q. | Montgomery GW et al. | — | 1993 | → |
| Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. | Schork NJ et al. | — | 1993 | → |
| Variance components for statistical genetics: applications in medical research to characteristics related to human diseases and health. | Hopper JL | — | 1993 | → |
| Analysis of factors influencing the efficacy of pooled platelet transfusions. | Matthews JP et al. | — | 1992 | → |
| Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome. | Ziv Y et al. | — | 1992 | → |
| Biochemical genetics of alcohol dehydrogenase isozymes in the gray short-tailed opossum (Monodelphis domestica). | Holmes RS et al. | — | 1992 | → |
| Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15. | Young K et al. | — | 1992 | → |
| Familiality and partitioning the variability of femoral bone mineral density in women of child-bearing age. | Sowers MR et al. | — | 1992 | → |
| Fixed and random effects in the variation of the finger ridge count: a study of fragile-X families. | Loesch DZ et al. | — | 1992 | → |
| Genetic analysis of sexual dimorphism in serum apo AI and HDL-C concentrations in baboons. | Towne B et al. | — | 1992 | → |
| Likelihood-based analyses of longitudinal twin and family data: experiences with pedigree-based approaches. | Williams CJ et al. | — | 1992 | → |
| Linkage heterogeneity between the C3 and LDLR and the APOA4 and APOA1 loci in baboons. | Kammerer CM et al. | — | 1992 | → |
| Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. | Dlouhy SR et al. | — | 1992 | → |
| Longitudinal studies with continuous responses. | Laird NM et al. | — | 1992 | → |
| Plots for examination of univariate twin data. | Williams CJ et al. | — | 1992 | → |
| Program of the 17th Annual Meeting of the Human Biology Council to be held in Las Vegas, Nevada Riviera Hotel March 31-April 1, 1992. | — | — | 1992 | → |
| TWINAN90: a FORTRAN program for conducting ANOVA-based and likelihood-based analyses of twin data. | Williams CJ et al. | — | 1992 | → |
| Allele frequency estimation from data on relatives. | Boehnke M | — | 1991 | → |
| A multipoint linkage map of the distal short arm of the human X chromosome. | Johnson CL et al. | — | 1991 | → |
| Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr). | Iannuzzi MC et al. | — | 1991 | → |
| A random walk method for computing genetic location scores. | Lange K et al. | — | 1991 | → |
| Biochemical and genetic analysis of a child with cystic fibrosis and cystinosis. | Smith ML et al. | — | 1991 | → |
| Genetic linkage analysis and homology relationships of genes located on human chromosome 11q. | Charmley P et al. | — | 1991 | → |
| Genetic susceptibility to naevi--a twin study. | Easton DF et al. | — | 1991 | → |
| Genomic structure of the human prion protein gene. | Puckett C et al. | — | 1991 | → |
| Inclusion of data on relatives for estimation of allele frequencies. | Chakraborty R | — | 1991 | → |
| Informativeness of twin-nuclear family and nuclear family designs for segregation analysis. | Duffy DL et al. | — | 1991 | → |
| Linkage of plasminogen (PLG) and apolipoprotein(a) (LPA) in baboons. | VandeBerg JL et al. | — | 1991 | → |
| Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium. | Foroud T et al. | — | 1991 | → |
| Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease. | Miller JL et al. | — | 1991 | → |
| Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. | Goradia TM et al. | — | 1991 | → |
| Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers. The MEN 2A International Collaborative Group. | Mathew CG et al. | — | 1991 | → |
| Rhodopsin Thr58Arg mutation in a family with autosomal dominant retinitis pigmentosa. | Richards JE et al. | — | 1991 | → |
| Statistical methods for multipoint radiation hybrid mapping. | Boehnke M et al. | — | 1991 | → |
| The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23. | Ziv Y et al. | — | 1991 | → |
| A primary linkage map of the human chromosome 11q22-23 region. | Charmley P et al. | — | 1990 | → |
| Estimating the power of linkage analysis in hereditary breast cancer. | Narod SA et al. | — | 1990 | → |
| Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region. | Sanal O et al. | — | 1990 | → |
| Haplotyping the human T-cell receptor beta-chain gene complex by use of restriction fragment length polymorphisms. | Charmley P et al. | — | 1990 | → |
| Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes. | Sieving PA et al. | — | 1990 | → |
| Sample-size guidelines for linkage analysis of a dominant locus for a quantitative trait by the method of lod scores. | Boehnke M | — | 1990 | → |
| Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance. | Risch NJ et al. | — | 1990 | → |
| Selecting pedigrees for linkage analysis of a quantitative trait: the expected number of informative meioses. | Boehnke M et al. | — | 1990 | → |
| Social contact and sibling similarity: facts, issues, and red herrings. | Rose RJ et al. | — | 1990 | → |
| The ataxia-telangiectasia gene (ATA) on chromosome II is distinct from the ETS-1 gene. | Concannon P et al. | — | 1990 | → |
| Alternative genetic models for the inheritance of the phenylthiocarbamide taste deficiency. | Olson JM et al. | — | 1989 | → |
| Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. | Ping AJ et al. | — | 1989 | → |
| Identification of LDL receptor gene marker associated with altered levels of LDL cholesterol and apolipoprotein B in baboons. | Hixson JE et al. | — | 1989 | → |
| Segregation analysis of quantitative traits in nuclear families: comparison of three program packages. | Konigsberg LW et al. | — | 1989 | → |
| Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers. | Cui XF et al. | — | 1989 | → |