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Pharmacogenetics and Genomics
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April 27, 2007
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach
Guy D Leschziner, Toby Andrew, John Paul Leach, et al.
European Journal of Human Genetics : EJHG
|
December 28, 2024
Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood
Niamh R Wilkinson, Elena Cervi, Bart Wagner, et al.
American Journal of Human Genetics
|
January 10, 2006
Mapping genetic loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs
Toby Andrew, Abraham Aviv, Mario Falchi, et al.
Statistical Applications in Genetics and Molecular Biology
|
May 2, 2006
A family-based association test for repeatedly measured quantitative traits adjusting for unknown environmental and/or polygenic effects
Christoph Lange, Kristel van Steen, Toby Andrew, et al.
Epilepsy Research
|
June 11, 2011
Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS)
Guy D Leschziner, Alison J Coffey, Toby Andrew, et al.
Investigative Ophthalmology & Visual Science
|
October 8, 2010
The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease
Samantha J Fahy, Cong Sun, Gu Zhu, et al.
Diabetes Care
|
June 12, 2021
Epigenome-Wide Association Study Reveals Methylation Loci Associated With Offspring Gestational Diabetes Mellitus Exposure and Maternal Methylome
Mickaël Canouil, Amna Khamis, Elina Keikkala, et al.
European Journal of Human Genetics : EJHG
|
January 5, 2006
Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort
Scott G Wilson, Gail Adam, Maria Langdown, et al.
Genome Research
|
March 12, 2010
Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains
Vardhman K Rakyan, Thomas A Down, Siarhei Maslau, et al.
The Lancet. Neurology
|
July 22, 2006
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study
Guy Leschziner, Andrea L Jorgensen, Toby Andrew, et al.
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of 7
Search research articles
Search
Showing results (41-50 of 61) with videos related to
Sort By:
Page
of 7
Pharmacogenetics and Genomics
|
April 27, 2007
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach
Guy D Leschziner, Toby Andrew, John Paul Leach, et al.
European Journal of Human Genetics : EJHG
|
December 28, 2024
Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood
Niamh R Wilkinson, Elena Cervi, Bart Wagner, et al.
American Journal of Human Genetics
|
January 10, 2006
Mapping genetic loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs
Toby Andrew, Abraham Aviv, Mario Falchi, et al.
Statistical Applications in Genetics and Molecular Biology
|
May 2, 2006
A family-based association test for repeatedly measured quantitative traits adjusting for unknown environmental and/or polygenic effects
Christoph Lange, Kristel van Steen, Toby Andrew, et al.
Epilepsy Research
|
June 11, 2011
Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS)
Guy D Leschziner, Alison J Coffey, Toby Andrew, et al.
Investigative Ophthalmology & Visual Science
|
October 8, 2010
The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease
Samantha J Fahy, Cong Sun, Gu Zhu, et al.
Diabetes Care
|
June 12, 2021
Epigenome-Wide Association Study Reveals Methylation Loci Associated With Offspring Gestational Diabetes Mellitus Exposure and Maternal Methylome
Mickaël Canouil, Amna Khamis, Elina Keikkala, et al.
European Journal of Human Genetics : EJHG
|
January 5, 2006
Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort
Scott G Wilson, Gail Adam, Maria Langdown, et al.
Genome Research
|
March 12, 2010
Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains
Vardhman K Rakyan, Thomas A Down, Siarhei Maslau, et al.
The Lancet. Neurology
|
July 22, 2006
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study
Guy Leschziner, Andrea L Jorgensen, Toby Andrew, et al.
Page
of 7