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Alexander F Wilson

Showing results (61-70 of 72) with videos related to

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Plos Genetics|October 21, 2014
Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysisAlexander Pemov, Heejong Sung, Paula L Hyland, et al.
Genetic Epidemiology|December 12, 2018
Linear mixed models for association analysis of quantitative traits with next-generation sequencing dataChi-Yang Chiu, Fang Yuan, Bing-Song Zhang, et al.
Journal of the American Statistical Association|July 29, 2021
Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular DegenerationYingda Jiang, Chi-Yang Chiu, Qi Yan, et al.
American Journal of Human Genetics|May 3, 2016
A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of CobalaminAnne M Molloy, Faith Pangilinan, James L Mills, 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.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2013
Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet diseaseYohei Kirino, Qing Zhou, Yoshiaki Ishigatsubo, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 26, 2012
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide associationKarl C Desch, Ayse B Ozel, David Siemieniak, et al.
American Journal of Human Genetics|July 5, 2003
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening setTara C Matise, Ravi Sachidanandam, Andrew G Clark, et al.
Nature Genetics|November 20, 2012
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9Cristina M Justice, Garima Yagnik, Yoonhee Kim, et al.
Human Genetics|April 9, 2020
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosisCristina M Justice, Araceli Cuellar, Krithi Bala, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
Plos Genetics|October 21, 2014
Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysisAlexander Pemov, Heejong Sung, Paula L Hyland, et al.
Genetic Epidemiology|December 12, 2018
Linear mixed models for association analysis of quantitative traits with next-generation sequencing dataChi-Yang Chiu, Fang Yuan, Bing-Song Zhang, et al.
Journal of the American Statistical Association|July 29, 2021
Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular DegenerationYingda Jiang, Chi-Yang Chiu, Qi Yan, et al.
American Journal of Human Genetics|May 3, 2016
A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of CobalaminAnne M Molloy, Faith Pangilinan, James L Mills, 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.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2013
Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet diseaseYohei Kirino, Qing Zhou, Yoshiaki Ishigatsubo, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 26, 2012
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide associationKarl C Desch, Ayse B Ozel, David Siemieniak, et al.
American Journal of Human Genetics|July 5, 2003
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening setTara C Matise, Ravi Sachidanandam, Andrew G Clark, et al.
Nature Genetics|November 20, 2012
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9Cristina M Justice, Garima Yagnik, Yoonhee Kim, et al.
Human Genetics|April 9, 2020
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosisCristina M Justice, Araceli Cuellar, Krithi Bala, et al.
Pageof 8