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Claes Wadelius

Showing results (71-80 of 80) with videos related to

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Human Molecular Genetics|October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarraysAlvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Science (New York, N.Y.)|August 11, 2007
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucomaGudmar Thorleifsson, Kristinn P Magnusson, Patrick Sulem, et al.
European Heart Journal|April 10, 2025
Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndromeAlex Hørby Christensen, Gang Pan, Rasmus L Marvig, et al.
Plos Biology|December 18, 2009
ZBED6, a novel transcription factor derived from a domesticated DNA transposon regulates IGF2 expression and muscle growthEllen Markljung, Lin Jiang, Jacob D Jaffe, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East EuropeAlessandra Maugeri, Kris Flothmann, Nadine Hemmrich, et al.
Nucleic Acids Research|November 17, 2007
ORegAnno: an open-access community-driven resource for regulatory annotationObi L Griffith, Stephen B Montgomery, Bridget Bernier, et al.
The Pharmacogenomics Journal|February 22, 2020
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatmentEva Rye Rasmussen, Pär Hallberg, Ekaterina V Baranova, et al.
Nature Genetics|September 14, 2010
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucomaGudmar Thorleifsson, G Bragi Walters, Alex W Hewitt, et al.
Nature|February 7, 2020
Analyses of non-coding somatic drivers in 2,658 cancer whole genomesEsther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, et al.
Nature|June 16, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project, Ewan Birney, John A Stamatoyannopoulos, et al.
Pageof 8

Showing results (71-80 of 80) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Human Molecular Genetics|October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarraysAlvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Science (New York, N.Y.)|August 11, 2007
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucomaGudmar Thorleifsson, Kristinn P Magnusson, Patrick Sulem, et al.
European Heart Journal|April 10, 2025
Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndromeAlex Hørby Christensen, Gang Pan, Rasmus L Marvig, et al.
Plos Biology|December 18, 2009
ZBED6, a novel transcription factor derived from a domesticated DNA transposon regulates IGF2 expression and muscle growthEllen Markljung, Lin Jiang, Jacob D Jaffe, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East EuropeAlessandra Maugeri, Kris Flothmann, Nadine Hemmrich, et al.
Nucleic Acids Research|November 17, 2007
ORegAnno: an open-access community-driven resource for regulatory annotationObi L Griffith, Stephen B Montgomery, Bridget Bernier, et al.
The Pharmacogenomics Journal|February 22, 2020
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatmentEva Rye Rasmussen, Pär Hallberg, Ekaterina V Baranova, et al.
Nature Genetics|September 14, 2010
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucomaGudmar Thorleifsson, G Bragi Walters, Alex W Hewitt, et al.
Nature|February 7, 2020
Analyses of non-coding somatic drivers in 2,658 cancer whole genomesEsther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, et al.
Nature|June 16, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project, Ewan Birney, John A Stamatoyannopoulos, et al.
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