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Mark Lathrop

Showing results (381-390 of 443) with videos related to

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JAMA|May 13, 2010
Genome-wide analysis of genetic loci associated with Alzheimer diseaseSudha Seshadri, Annette L Fitzpatrick, M Arfan Ikram, et al.
Carcinogenesis|September 13, 2015
Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortiaDarren R Brenner, Christopher I Amos, Yonathan Brhane, et al.
Nature Communications|March 5, 2026
A gut microbiome-kidney-heart axis predictive of future cardiovascular diseasesKanta Chechi, Rima Chakaroun, Antonis Myridakis, et al.
American Journal of Human Genetics|March 1, 2011
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderSven Cichon, Thomas W Mühleisen, Franziska A Degenhardt, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 5, 2014
A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any ageHabibul Ahsan, Jerry Halpern, Muhammad G Kibriya, et al.
Human Genetics|August 14, 2012
Genome-wide association study of glioma and meta-analysisPreetha Rajaraman, Beatrice S Melin, Zhaoming Wang, et al.
Brain : a Journal of Neurology|May 5, 2022
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidateAniket Mishra, Cécile Duplaà, Dina Vojinovic, et al.
Plos One|November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokeJohn W Cole, Huichun Xu, Kathleen Ryan, et al.
Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
American Journal of Human Genetics|June 11, 2021
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individualsJack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, et al.
Pageof 45

Showing results (381-390 of 443) with videos related to

Sort By:
Pageof 45
JAMA|May 13, 2010
Genome-wide analysis of genetic loci associated with Alzheimer diseaseSudha Seshadri, Annette L Fitzpatrick, M Arfan Ikram, et al.
Carcinogenesis|September 13, 2015
Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortiaDarren R Brenner, Christopher I Amos, Yonathan Brhane, et al.
Nature Communications|March 5, 2026
A gut microbiome-kidney-heart axis predictive of future cardiovascular diseasesKanta Chechi, Rima Chakaroun, Antonis Myridakis, et al.
American Journal of Human Genetics|March 1, 2011
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderSven Cichon, Thomas W Mühleisen, Franziska A Degenhardt, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 5, 2014
A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any ageHabibul Ahsan, Jerry Halpern, Muhammad G Kibriya, et al.
Human Genetics|August 14, 2012
Genome-wide association study of glioma and meta-analysisPreetha Rajaraman, Beatrice S Melin, Zhaoming Wang, et al.
Brain : a Journal of Neurology|May 5, 2022
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidateAniket Mishra, Cécile Duplaà, Dina Vojinovic, et al.
Plos One|November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokeJohn W Cole, Huichun Xu, Kathleen Ryan, et al.
Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
American Journal of Human Genetics|June 11, 2021
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individualsJack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, et al.
Pageof 45