Found: 24
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A Rare Variant in MDH2 (rs111879470) Is Associated with Predisposition to Recurrent Breast Cancer in an Extended High-Risk Pedigree.
- Published in:
- Cancers, 2023, v. 15, n. 24, p. 5851, doi. 10.3390/cancers15245851
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- Publication type:
- Article
High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer.
- Published in:
- Cancers, 2023, v. 15, n. 7, p. 2085, doi. 10.3390/cancers15072085
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- Publication type:
- Article
Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience.
- Published in:
- 2018
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- Publication type:
- Correction Notice
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience.
- Published in:
- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0486-1
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- Publication type:
- Article
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 6, p. 943, doi. 10.1111/cge.13757
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- Publication type:
- Article
Adrenal-Permissive Germline HSD3B1 Allele and Prostate Cancer Outcomes.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 3, p. e242976, doi. 10.1001/jamanetworkopen.2024.2976
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- Publication type:
- Article
Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 5, p. 636, doi. 10.1038/ejhg.2008.236
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- Publication type:
- Article
Prostate cancer risk prediction based on complete prostate cancer family history.
- Published in:
- Prostate, 2015, v. 75, n. 4, p. 390, doi. 10.1002/pros.22925
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- Publication type:
- Article
Identification of specific Y chromosomes associated with increased prostate cancer risk.
- Published in:
- Prostate, 2014, v. 74, n. 9, p. 991, doi. 10.1002/pros.22821
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- Publication type:
- Article
FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 12, p. 1, doi. 10.1002/mgg3.1532
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- Publication type:
- Article
Genome-wide analysis of high-risk primary brain cancer pedigrees identifies PDXDC1 as a candidate brain cancer predisposition gene.
- Published in:
- Neuro-Oncology, 2021, v. 23, n. 2, p. 277, doi. 10.1093/neuonc/noaa161
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- Publication type:
- Article
Legal terms of use and public genealogy websites.
- Published in:
- Journal of Law & the Biosciences, 2020, v. 7, n. 1, p. 1, doi. 10.1093/jlb/lsaa063
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- Publication type:
- Article
Evidence of an Inherited Predisposition for Spinal Cord Tumors.
- Published in:
- Global Spine Journal, 2018, v. 8, n. 4, p. 340, doi. 10.1177/2192568217725717
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- Publication type:
- Article
Analysis of high‐risk pedigrees identifies 11 candidate variants for Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 2, p. 307, doi. 10.1002/alz.12397
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- Publication type:
- Article
Comorbidity and Cancer Disease Rates among Those at High-Risk for Alzheimer's Disease: A Population Database Analysis.
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- International Journal of Environmental Research & Public Health, 2022, v. 19, n. 24, p. 16419, doi. 10.3390/ijerph192416419
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- Publication type:
- Article
Genetic risk and likelihood of prostate cancer detection on first biopsy by ancestry.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2024, v. 116, n. 5, p. 753, doi. 10.1093/jnci/djae002
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- Publication type:
- Article
A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma.
- Published in:
- 2018
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- Publication type:
- journal article
An Application of the Latent p Value Method to Assess Linkage in Asthma Pedigrees.
- Published in:
- Human Heredity, 2010, v. 70, n. 1, p. 1, doi. 10.1159/000291915
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- Publication type:
- Article
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
- Published in:
- JAMA Network Open, 2019, v. 2, n. 3, p. e191350, doi. 10.1001/jamanetworkopen.2019.1350
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- Publication type:
- Article
Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears.
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- Orthopaedic Journal of Sports Medicine, 2016, v. 4, n. 4, p. 1, doi. 10.1177/2325967116642173
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- Publication type:
- Article
Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortia.
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- Human Molecular Genetics, 2024, v. 33, n. 8, p. 687, doi. 10.1093/hmg/ddae002
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- Publication type:
- Article
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer.
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- International Journal of Cancer, 2023, v. 153, n. 2, p. 364, doi. 10.1002/ijc.34510
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- Publication type:
- Article
A role for the MEGF6 gene in predisposition to osteoporosis.
- Published in:
- Annals of Human Genetics, 2021, v. 85, n. 2, p. 58, doi. 10.1111/ahg.12408
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- Publication type:
- Article
Linkage Analysis of Extended High-Risk Pedigrees Replicates a Cutaneous Malignant Melanoma Predisposition Locus on Chromosome 9q21.
- Published in:
- Journal of Investigative Dermatology, 2013, v. 133, n. 1, p. 128, doi. 10.1038/jid.2012.271
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- Publication type:
- Article