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Lon R Cardon

Showing results (81-90 of 102) with videos related to

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American Journal of Human Genetics|October 30, 2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United StatesClyde Francks, Silvia Paracchini, Shelley D Smith, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 18, 2011
Pazopanib efficacy in renal cell carcinoma: evidence for predictive genetic markers in angiogenesis-related and exposure-related genesChun-Fang Xu, Nan X Bing, Howard A Ball, et al.
Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.
Plos One|July 27, 2011
The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traitsJosine L Min, Jennifer M Taylor, J Brent Richards, et al.
Genetics|May 17, 2006
Fine-scale map of encyclopedia of DNA elements regions in the Korean populationYeon-Kyeong Yoo, Xiayi Ke, Sungwoo Hong, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 21, 2014
Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of PazopanibMichael L Maitland, Chun-Fang Xu, Yu-Ching Cheng, et al.
Nature|July 12, 2002
A first-generation linkage disequilibrium map of human chromosome 22Elisabeth Dawson, Gonçalo R Abecasis, Suzannah Bumpstead, et al.
Diabetes|March 10, 2012
Deep resequencing unveils genetic architecture of ADIPOQ and identifies a novel low-frequency variant strongly associated with adiponectin variationLiling L Warren, Li Li, Matthew R Nelson, et al.
Heart Asia|June 22, 2016
Genome-wide association analysis and replication of coronary artery disease in South Korea suggests a causal variant common to diverse populationsEun Young Cho, Yangsoo Jang, Eun Soon Shin, et al.
European Journal of Human Genetics : EJHG|November 21, 2008
Investigation of the fine structure of European populations with applications to disease association studiesSimon C Heath, Ivo G Gut, Paul Brennan, et al.
Pageof 11

Showing results (81-90 of 102) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|October 30, 2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United StatesClyde Francks, Silvia Paracchini, Shelley D Smith, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 18, 2011
Pazopanib efficacy in renal cell carcinoma: evidence for predictive genetic markers in angiogenesis-related and exposure-related genesChun-Fang Xu, Nan X Bing, Howard A Ball, et al.
Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.
Plos One|July 27, 2011
The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traitsJosine L Min, Jennifer M Taylor, J Brent Richards, et al.
Genetics|May 17, 2006
Fine-scale map of encyclopedia of DNA elements regions in the Korean populationYeon-Kyeong Yoo, Xiayi Ke, Sungwoo Hong, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 21, 2014
Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of PazopanibMichael L Maitland, Chun-Fang Xu, Yu-Ching Cheng, et al.
Nature|July 12, 2002
A first-generation linkage disequilibrium map of human chromosome 22Elisabeth Dawson, Gonçalo R Abecasis, Suzannah Bumpstead, et al.
Diabetes|March 10, 2012
Deep resequencing unveils genetic architecture of ADIPOQ and identifies a novel low-frequency variant strongly associated with adiponectin variationLiling L Warren, Li Li, Matthew R Nelson, et al.
Heart Asia|June 22, 2016
Genome-wide association analysis and replication of coronary artery disease in South Korea suggests a causal variant common to diverse populationsEun Young Cho, Yangsoo Jang, Eun Soon Shin, et al.
European Journal of Human Genetics : EJHG|November 21, 2008
Investigation of the fine structure of European populations with applications to disease association studiesSimon C Heath, Ivo G Gut, Paul Brennan, et al.
Pageof 11