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Mark Lathrop

Showing results (241-250 of 443) with videos related to

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American Journal of Human Genetics|July 11, 2006
Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertensionChris Wallace, Ming-Zhan Xue, Stephen J Newhouse, et al.
Virchows Archiv : an International Journal of Pathology|January 6, 2021
Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on renal cancerBehnoush Abedi-Ardekani, Dariush Nasrollahzadeh, Lars Egevad, et al.
Nature Genetics|January 17, 2012
PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humansAnaïs Grall, Eric Guaguère, Sandrine Planchais, et al.
American Journal of Human Genetics|November 5, 2013
Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elementsElin Grundberg, Eshwar Meduri, Johanna K Sandling, et al.
Nature|February 25, 2015
An epigenome-wide association study of total serum immunoglobulin E concentrationLiming Liang, Saffron A G Willis-Owen, Catherine Laprise, et al.
Human Molecular Genetics|October 29, 2004
Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA familiesEmmanuelle Bouzigon, Marie-Hélène Dizier, Christine Krähenbühl, et al.
Archives of General Psychiatry|July 9, 2008
Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behaviorGunter Schumann, Monika Johann, Josef Frank, et al.
American Journal of Human Genetics|January 9, 2008
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemiaChris Wallace, Stephen J Newhouse, Peter Braund, et al.
Nature Communications|July 30, 2015
Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variantsFiona Allum, Xiaojian Shao, Frédéric Guénard, et al.
Nature Communications|May 30, 2015
Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variantsFiona Allum, Xiaojian Shao, Frédéric Guénard, et al.
Pageof 45

Showing results (241-250 of 443) with videos related to

Sort By:
Pageof 45
American Journal of Human Genetics|July 11, 2006
Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertensionChris Wallace, Ming-Zhan Xue, Stephen J Newhouse, et al.
Virchows Archiv : an International Journal of Pathology|January 6, 2021
Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on renal cancerBehnoush Abedi-Ardekani, Dariush Nasrollahzadeh, Lars Egevad, et al.
Nature Genetics|January 17, 2012
PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humansAnaïs Grall, Eric Guaguère, Sandrine Planchais, et al.
American Journal of Human Genetics|November 5, 2013
Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elementsElin Grundberg, Eshwar Meduri, Johanna K Sandling, et al.
Nature|February 25, 2015
An epigenome-wide association study of total serum immunoglobulin E concentrationLiming Liang, Saffron A G Willis-Owen, Catherine Laprise, et al.
Human Molecular Genetics|October 29, 2004
Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA familiesEmmanuelle Bouzigon, Marie-Hélène Dizier, Christine Krähenbühl, et al.
Archives of General Psychiatry|July 9, 2008
Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behaviorGunter Schumann, Monika Johann, Josef Frank, et al.
American Journal of Human Genetics|January 9, 2008
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemiaChris Wallace, Stephen J Newhouse, Peter Braund, et al.
Nature Communications|July 30, 2015
Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variantsFiona Allum, Xiaojian Shao, Frédéric Guénard, et al.
Nature Communications|May 30, 2015
Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variantsFiona Allum, Xiaojian Shao, Frédéric Guénard, et al.
Pageof 45