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Scott M Williams

Showing results (201-210 of 260) with videos related to

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Human Genetics|May 27, 2016
Epigenetic and genetic variation in GATA5 is associated with gastric disease riskRafal S Sobota, Nuri Kodaman, Robertino Mera, et al.
Gastroenterology|October 15, 2011
Increased variance in germline allele-specific expression of APC associates with colorectal cancerMaria Cristina Curia, Sabrina De Iure, Laura De Lellis, et al.
Biodata Mining|July 30, 2014
Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factorsTimothy H Ciesielski, Sarah A Pendergrass, Marquitta J White, et al.
Plos Genetics|September 4, 2025
Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic reviewShiying Liu, William S Bush, Rufus Olusola Akinyemi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic reviewShiying Liu, William S Bush, Rufus Olusola Akinyemi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.
Plos Genetics|May 1, 2020
Interaction between host genes and Mycobacterium tuberculosis lineage can affect tuberculosis severity: Evidence for coevolution?Michael L McHenry, Jacquelaine Bartlett, Robert P Igo, et al.
Plos Pathogens|March 23, 2012
HMOX1 gene promoter alleles and high HO-1 levels are associated with severe malaria in Gambian childrenMichael Walther, Adam De Caul, Peter Aka, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 29, 2025
Basic Science and PathogenesisTimothy H Ciesielski, Neetesh Pandey, Farid Rajabli, et al.
Plos Genetics|November 19, 2013
Recurrent tissue-specific mtDNA mutations are common in humansDavid C Samuels, Chun Li, Bingshan Li, et al.
Pageof 26

Showing results (201-210 of 260) with videos related to

Sort By:
Pageof 26
Human Genetics|May 27, 2016
Epigenetic and genetic variation in GATA5 is associated with gastric disease riskRafal S Sobota, Nuri Kodaman, Robertino Mera, et al.
Gastroenterology|October 15, 2011
Increased variance in germline allele-specific expression of APC associates with colorectal cancerMaria Cristina Curia, Sabrina De Iure, Laura De Lellis, et al.
Biodata Mining|July 30, 2014
Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factorsTimothy H Ciesielski, Sarah A Pendergrass, Marquitta J White, et al.
Plos Genetics|September 4, 2025
Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic reviewShiying Liu, William S Bush, Rufus Olusola Akinyemi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic reviewShiying Liu, William S Bush, Rufus Olusola Akinyemi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.
Plos Genetics|May 1, 2020
Interaction between host genes and Mycobacterium tuberculosis lineage can affect tuberculosis severity: Evidence for coevolution?Michael L McHenry, Jacquelaine Bartlett, Robert P Igo, et al.
Plos Pathogens|March 23, 2012
HMOX1 gene promoter alleles and high HO-1 levels are associated with severe malaria in Gambian childrenMichael Walther, Adam De Caul, Peter Aka, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 29, 2025
Basic Science and PathogenesisTimothy H Ciesielski, Neetesh Pandey, Farid Rajabli, et al.
Plos Genetics|November 19, 2013
Recurrent tissue-specific mtDNA mutations are common in humansDavid C Samuels, Chun Li, Bingshan Li, et al.
Pageof 26