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Arthur S Lee

Showing results (1-10 of 16) with videos related to

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Human Molecular Genetics|January 9, 2008
Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studiesArthur S Lee, María Gutiérrez-Arcelus, George H Perry, et al.
Human Genetics|February 28, 2012
Evolutionary genetics of the human Rh blood group systemGeorge H Perry, Yali Xue, Richard S Smith, et al.
Nature Genetics|September 11, 2007
Diet and the evolution of human amylase gene copy number variationGeorge H Perry, Nathaniel J Dominy, Katrina G Claw, et al.
Genome Research|September 9, 2008
Copy number variation and evolution in humans and chimpanzeesGeorge H Perry, Fengtang Yang, Tomas Marques-Bonet, et al.
Nature Communications|October 13, 2019
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertilityArthur S Lee, Jannette Rusch, Ana C Lima, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2011
Extensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysisKim H Brown, Kimberly P Dobrinski, Arthur S Lee, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Large-scale discovery of neural enhancers for cis-regulation therapiesTroy A McDiarmid, Nicholas F Page, Florence M Chardon, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Nature Communications|September 27, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
Comprehensive analysis of <i>de novo</i> variants across 2,497 orofacial cleft trios reveals novel genetic drivers of diseaseNehir E Kurtas, Alba Sanchis-Juan, Eren Shin, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|January 9, 2008
Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studiesArthur S Lee, María Gutiérrez-Arcelus, George H Perry, et al.
Human Genetics|February 28, 2012
Evolutionary genetics of the human Rh blood group systemGeorge H Perry, Yali Xue, Richard S Smith, et al.
Nature Genetics|September 11, 2007
Diet and the evolution of human amylase gene copy number variationGeorge H Perry, Nathaniel J Dominy, Katrina G Claw, et al.
Genome Research|September 9, 2008
Copy number variation and evolution in humans and chimpanzeesGeorge H Perry, Fengtang Yang, Tomas Marques-Bonet, et al.
Nature Communications|October 13, 2019
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertilityArthur S Lee, Jannette Rusch, Ana C Lima, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2011
Extensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysisKim H Brown, Kimberly P Dobrinski, Arthur S Lee, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Large-scale discovery of neural enhancers for cis-regulation therapiesTroy A McDiarmid, Nicholas F Page, Florence M Chardon, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Nature Communications|September 27, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
Comprehensive analysis of <i>de novo</i> variants across 2,497 orofacial cleft trios reveals novel genetic drivers of diseaseNehir E Kurtas, Alba Sanchis-Juan, Eren Shin, et al.
Pageof 2