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- Published in:
- JNCI: Journal of the National Cancer Institute, 1991, v. 83, n. 1, p. 65, doi. 10.1093/jnci/83.1.65
- By:
- Publication type:
- Article
Evidence for Mendelian Inheritance in the Pathogenesis of Lung Cancer.
- Published in:
- JNCI: Journal of the National Cancer Institute, 1990, v. 82, n. 15, p. 1272
- By:
- Publication type:
- Article
Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic Amenorrhea.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Complex N-Linked Glycosylation: A Potential Modifier of Niemann–Pick Disease, Type C1 Pathology.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 9, p. 5082, doi. 10.3390/ijms23095082
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- Publication type:
- Article
What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics.
- Published in:
- Human Genetics, 2022, v. 141, n. 9, p. 1515, doi. 10.1007/s00439-021-02402-z
- By:
- Publication type:
- Article
A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 8, p. 1, doi. 10.1002/mgg3.2179
- By:
- Publication type:
- Article
r2VIM: A new variable selection method for random forests in genome-wide association studies.
- Published in:
- BioData Mining, 2016, v. 9, p. 1, doi. 10.1186/s13040-016-0087-3
- By:
- Publication type:
- Article
Risk estimation using probability machines.
- Published in:
- BioData Mining, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1756-0381-7-2
- By:
- Publication type:
- Article
Hereditary nonpolyposis colorectal cancer (Lynch syndromes I and II). I. Clinical description of resource.
- Published in:
- 1985
- By:
- Publication type:
- journal article
Hereditary nonpolyposis colorectal cancer (Lynch syndromes I and II). II. Biomarker studies.
- Published in:
- 1985
- By:
- Publication type:
- journal article
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 8, p. 1, doi. 10.1371/journal.pgen.1007532
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- Publication type:
- Article
Genetic analysis of human breast cancer: Literature review and description of family data in workshop.
- Published in:
- Genetic Epidemiology, 1986, v. 3, n. S1, p. 1, doi. 10.1002/gepi.1370030704
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- Publication type:
- Article
Genetic analysis of human breast cancer: A synthesis of contributions to Gaw IV.
- Published in:
- Genetic Epidemiology, 1986, v. 3, n. S1, p. 15, doi. 10.1002/gepi.1370030705
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- Publication type:
- Article
Critique of a published analysis of the Jacobsen data.
- Published in:
- Genetic Epidemiology, 1986, v. 3, n. S1, p. 55, doi. 10.1002/gepi.1370030709
- By:
- Publication type:
- Article
Segregation analysis of hereditary nonpolyposis colorectal cancer.
- Published in:
- Genetic Epidemiology, 1986, v. 3, n. 1, p. 27, doi. 10.1002/gepi.1370030104
- By:
- Publication type:
- Article
Genes, environment and the value of prospective cohort studies.
- Published in:
- Nature Reviews Genetics, 2006, v. 7, n. 10, p. 812, doi. 10.1038/nrg1919
- By:
- Publication type:
- Article
Rare copy number variants in patients with congenital conotruncal heart defects.
- Published in:
- Birth Defects Research, 2017, v. 109, n. 4, p. 271, doi. 10.1002/bdra.23609
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- Publication type:
- Article
Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.
- Published in:
- Human Genetics, 2019, v. 138, n. 4, p. 339, doi. 10.1007/s00439-019-01991-0
- By:
- Publication type:
- Article
Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.
- Published in:
- Human Genetics, 2006, v. 120, n. 1, p. 31, doi. 10.1007/s00439-006-0163-8
- By:
- Publication type:
- Article
Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect.
- Published in:
- Human Genetics, 2006, v. 118, n. 6, p. 716, doi. 10.1007/s00439-005-0099-4
- By:
- Publication type:
- Article
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region.
- Published in:
- 2005
- By:
- Publication type:
- Correction Notice
Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer.
- Published in:
- Human Genetics, 2000, v. 107, n. 4, p. 372, doi. 10.1007/s004390000384
- By:
- Publication type:
- Article
Combined Genome-Wide Scan for Prostate Cancer Susceptibility Genes.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2004, v. 96, n. 16, p. 1240, doi. 10.1093/jnci/djh228
- By:
- Publication type:
- Article
Sterol and lipid analyses identifies hypolipidemia and apolipoprotein disorders in autism associated with adaptive functioning deficits.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01580-8
- By:
- Publication type:
- Article
Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 437, doi. 10.1038/ejhg.2012.185
- By:
- Publication type:
- Article
ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 8, p. 983, doi. 10.1038/ejhg.2008.43
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- Publication type:
- Article
Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1018, doi. 10.1038/sj.ejhg.5201650
- By:
- Publication type:
- Article
Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutations.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 11, p. 899, doi. 10.1038/sj.ejhg.5201256
- By:
- Publication type:
- Article
Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 11, p. 835, doi. 10.1038/sj.ejhg.5201052
- By:
- Publication type:
- Article
Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.
- Published in:
- BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0752-8
- By:
- Publication type:
- Article
GeneLink: a database to facilitate genetic studies of complex traits.
- Published in:
- BMC Genomics, 2004, v. 5, p. 81, doi. 10.1186/1471-2164-5-81
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- Publication type:
- Article
Replicating genotype–phenotype associations.
- Published in:
- Nature, 2007, v. 447, n. 7145, p. 655, doi. 10.1038/447655a
- By:
- Publication type:
- Article
Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.
- Published in:
- 2021
- By:
- Publication type:
- journal article
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer.
- Published in:
- International Journal of Cancer, 2023, v. 153, n. 2, p. 364, doi. 10.1002/ijc.34510
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- Publication type:
- Article
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder.
- Published in:
- BMC Genetics, 2015, v. 16, n. 1, p. 2, doi. 10.1186/s12863-015-0184-1
- By:
- Publication type:
- Article
Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment.
- Published in:
- BMC Genetics, 2006, v. 7, p. 21, doi. 10.1186/1471-2156-7-21
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- Publication type:
- Article
Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans.
- Published in:
- BMC Genetics, 2005, v. 6, p. S1, doi. 10.1186/1471-2156-6-S1-S1
- By:
- Publication type:
- Article
Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis.
- Published in:
- BMC Genetics, 2003, v. 4, p. S73, doi. 10.1186/1471-2156-4-S1-S73
- By:
- Publication type:
- Article
Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors.
- Published in:
- BMC Genetics, 2003, v. 4, p. S1, doi. 10.1186/1471-2156-4-S1-S1
- By:
- Publication type:
- Article
Inferring relationships between pairs of individuals from locus heterozygosities.
- Published in:
- BMC Genetics, 2002, v. 3, p. 23, doi. 10.1186/1471-2156-3-23
- By:
- Publication type:
- Article
Myopia in Chinese families shows linkage to 10q26.13.
- Published in:
- Molecular Vision, 2018, v. 24, p. 29
- By:
- Publication type:
- Article
CELLULAR GENES IN THE MOUSE REGULATE IN TRANS THE EXPRESSION OF ENDOGENOUS MOUSE MAMMARY TUMOR VIRUSES.
- Published in:
- Genetics, 1985, v. 111, n. 3, p. 597
- By:
- Publication type:
- Article
Transmission/disequilibrium tests of androgen receptor and glutathione S-transferase pi variants in prostate cancer families.
- Published in:
- International Journal of Cancer, 2002, v. 98, n. 6, p. 938, doi. 10.1002/ijc.10290
- By:
- Publication type:
- Article
INCREASED FAMILIAL RISK FOR NON-LUNG CANCER AMONG RELATWES OF LUNG CANCER PATIENTS.
- Published in:
- American Journal of Epidemiology, 1987, v. 126, n. 2, p. 237, doi. 10.1093/aje/126.2.237
- By:
- Publication type:
- Article
8q24 risk alleles and prostate cancer in African-Barbadian men.
- Published in:
- Prostate, 2014, v. 74, n. 16, p. 1579, doi. 10.1002/pros.22871
- By:
- Publication type:
- Article
Suggestive evidence of linkage identified at chromosomes 12q24 and 2p16 in African American prostate cancer families from louisiana.
- Published in:
- Prostate, 2012, v. 72, n. 9, p. 938, doi. 10.1002/pros.21496
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- Publication type:
- Article
Contribution of HPC1 ( RNASEL) and HPCX variants to prostate cancer in a founder population.
- Published in:
- Prostate, 2010, v. 70, n. 15, p. 1716, doi. 10.1002/pros.21207
- By:
- Publication type:
- Article
Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for prostate cancer Genetics using novel sumLINK and sumLOD analyses.
- Published in:
- Prostate, 2010, v. 70, n. 7, p. 735, doi. 10.1002/pros.21106
- By:
- Publication type:
- Article
Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26(Johanna Schleutker, Agnes B. Baffoe-Bonnie, and Elizabeth Gillanders contributed equally to this study.).
- Published in:
- Prostate, 2003, v. 57, n. 4, p. 280, doi. 10.1002/pros.10302
- By:
- Publication type:
- Article
Estimation of Linkage and Association from Allele Transmission Data.
- Published in:
- Biometrical Journal, 2003, v. 45, n. 3, p. 349
- By:
- Publication type:
- Article