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Naisha Shah

Showing results (21-30 of 26) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 21, 2018
Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adultsBradley A Perkins, C Thomas Caskey, Pamila Brar, et al.
Nature Medicine|October 27, 2015
Genome-wide identification of microRNAs regulating cholesterol and triglyceride homeostasisAlexandre Wagschal, S Hani Najafi-Shoushtari, Lifeng Wang, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
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Showing results (21-30 of 26) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2018
Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adultsBradley A Perkins, C Thomas Caskey, Pamila Brar, et al.
Nature Medicine|October 27, 2015
Genome-wide identification of microRNAs regulating cholesterol and triglyceride homeostasisAlexandre Wagschal, S Hani Najafi-Shoushtari, Lifeng Wang, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
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