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Nancy F Hansen

Showing results (31-40 of 53) with videos related to

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Plos Genetics|August 23, 2012
Mutational signatures of de-differentiation in functional non-coding regions of melanoma genomesStephen C J Parker, Jared Gartner, Isabel Cardenas-Navia, et al.
American Journal of Human Genetics|May 27, 2014
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT intervalAshish Kapoor, Rajesh B Sekar, Nancy F Hansen, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Plos Genetics|October 25, 2011
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteasesTyler Mark Pierson, David Adams, Florian Bonn, et al.
Genome Research|July 16, 2009
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicineLeslie G Biesecker, James C Mullikin, Flavia M Facio, et al.
Genome Research|October 14, 2004
An intermediate grade of finished genomic sequence suitable for comparative analysesRobert W Blakesley, Nancy F Hansen, James C Mullikin, et al.
Biorxiv : the Preprint Server for Biology|April 29, 2026
The complete genome of the KOLF2.1J reference iPSC linePilar Alvarez Jerez, Arang Rhie, Juhyun Kim, et al.
Plos Genetics|September 9, 2011
Predisposition to cancer caused by genetic and functional defects of mammalian Atad5Daphne W Bell, Nilabja Sikdar, Kyoo-Young Lee, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Plos Genetics|August 23, 2012
Mutational signatures of de-differentiation in functional non-coding regions of melanoma genomesStephen C J Parker, Jared Gartner, Isabel Cardenas-Navia, et al.
American Journal of Human Genetics|May 27, 2014
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT intervalAshish Kapoor, Rajesh B Sekar, Nancy F Hansen, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Plos Genetics|October 25, 2011
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteasesTyler Mark Pierson, David Adams, Florian Bonn, et al.
Genome Research|July 16, 2009
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicineLeslie G Biesecker, James C Mullikin, Flavia M Facio, et al.
Genome Research|October 14, 2004
An intermediate grade of finished genomic sequence suitable for comparative analysesRobert W Blakesley, Nancy F Hansen, James C Mullikin, et al.
Biorxiv : the Preprint Server for Biology|April 29, 2026
The complete genome of the KOLF2.1J reference iPSC linePilar Alvarez Jerez, Arang Rhie, Juhyun Kim, et al.
Plos Genetics|September 9, 2011
Predisposition to cancer caused by genetic and functional defects of mammalian Atad5Daphne W Bell, Nilabja Sikdar, Kyoo-Young Lee, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Pageof 6