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Mark Lathrop

Showing results (351-360 of 443) with videos related to

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Nature Genetics|January 15, 2008
Newly identified loci that influence lipid concentrations and risk of coronary artery diseaseCristen J Willer, Serena Sanna, Anne U Jackson, et al.
Nature Aging|November 20, 2025
Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel diseaseIlana Caro, Daniel Western, Shinichi Namba, et al.
Nature|December 4, 2015
Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinomaCorine Bertolotto, Fabienne Lesueur, Sandy Giuliano, et al.
Research Square|July 16, 2024
Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel diseaseStephanie Debette, Ilana Caro, Daniel Western, et al.
Plos One|February 13, 2014
Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk geneYukinori Okada, Dorothee Diogo, Jeffrey D Greenberg, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 20, 2009
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosisJohn E Landers, Judith Melki, Vincent Meininger, et al.
Nature Communications|October 30, 2014
Variation in genomic landscape of clear cell renal cell carcinoma across EuropeGhislaine Scelo, Yasser Riazalhosseini, Liliana Greger, et al.
The Journal of Clinical Investigation|May 27, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Pageof 45

Showing results (351-360 of 443) with videos related to

Sort By:
Pageof 45
Nature Genetics|January 15, 2008
Newly identified loci that influence lipid concentrations and risk of coronary artery diseaseCristen J Willer, Serena Sanna, Anne U Jackson, et al.
Nature Aging|November 20, 2025
Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel diseaseIlana Caro, Daniel Western, Shinichi Namba, et al.
Nature|December 4, 2015
Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinomaCorine Bertolotto, Fabienne Lesueur, Sandy Giuliano, et al.
Research Square|July 16, 2024
Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel diseaseStephanie Debette, Ilana Caro, Daniel Western, et al.
Plos One|February 13, 2014
Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk geneYukinori Okada, Dorothee Diogo, Jeffrey D Greenberg, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 20, 2009
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosisJohn E Landers, Judith Melki, Vincent Meininger, et al.
Nature Communications|October 30, 2014
Variation in genomic landscape of clear cell renal cell carcinoma across EuropeGhislaine Scelo, Yasser Riazalhosseini, Liliana Greger, et al.
The Journal of Clinical Investigation|May 27, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Pageof 45