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Showing results (1041-1050 of 1,082) with videos related to
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Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort
Lara M Lange, Catalina Cerquera-Cleves, Ai Huey Tan, et al.
Human Genetics
|
June 6, 2016
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
Craig C Teerlink, Daniel Leongamornlert, Tokhir Dadaev, et al.
American Journal of Human Genetics
|
September 27, 2016
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, et al.
Parkinsonism & Related Disorders
|
August 1, 2025
Validation of clinical ratings of cervical dystonia using computer-generated avatars
Sebastian Loens, Roland Stenger, Feline Hamami, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance
Lara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Human Genetics
|
December 27, 2011
Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)
Guangfu Jin, Lingyi Lu, Kathleen A Cooney, et al.
The Lancet. Neurology
|
July 15, 2026
Parkinson's disease genetics across diverse ancestries: an observational genetic study of causal and risk variants with translational implications
Lara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Human Molecular Genetics
|
May 5, 2007
Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics
Nicola J Camp, Lisa A Cannon-Albright, James M Farnham, et al.
Frontiers in Genetics
|
January 1, 2024
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program
Nicole D Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, et al.
Trials
|
August 21, 2015
Multimodal treatment of perianal fistulas in Crohn's disease: seton versus anti-TNF versus advancement plasty (PISA): study protocol for a randomized controlled trial
E Joline de Groof, Christianne J Buskens, Cyriel Y Ponsioen, et al.
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Search research articles
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Showing results (1041-1050 of 1,082) with videos related to
Sort By:
Page
of 109
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort
Lara M Lange, Catalina Cerquera-Cleves, Ai Huey Tan, et al.
Human Genetics
|
June 6, 2016
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
Craig C Teerlink, Daniel Leongamornlert, Tokhir Dadaev, et al.
American Journal of Human Genetics
|
September 27, 2016
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, et al.
Parkinsonism & Related Disorders
|
August 1, 2025
Validation of clinical ratings of cervical dystonia using computer-generated avatars
Sebastian Loens, Roland Stenger, Feline Hamami, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance
Lara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Human Genetics
|
December 27, 2011
Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)
Guangfu Jin, Lingyi Lu, Kathleen A Cooney, et al.
The Lancet. Neurology
|
July 15, 2026
Parkinson's disease genetics across diverse ancestries: an observational genetic study of causal and risk variants with translational implications
Lara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Human Molecular Genetics
|
May 5, 2007
Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics
Nicola J Camp, Lisa A Cannon-Albright, James M Farnham, et al.
Frontiers in Genetics
|
January 1, 2024
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program
Nicole D Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, et al.
Trials
|
August 21, 2015
Multimodal treatment of perianal fistulas in Crohn's disease: seton versus anti-TNF versus advancement plasty (PISA): study protocol for a randomized controlled trial
E Joline de Groof, Christianne J Buskens, Cyriel Y Ponsioen, et al.
Page
of 109