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Elise Ruark

Showing results (11-20 of 28) with videos related to

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Breast Cancer Research and Treatment|April 25, 2012
Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancerKatie Snape, Elise Ruark, Patrick Tarpey, et al.
F1000Research|February 3, 2016
The ICR1000 UK exome series: a resource of gene variation in an outbred populationElise Ruark, Márton Münz, Anthony Renwick, et al.
Scientific Reports|July 14, 2016
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patientsAngela George, Daniel Riddell, Sheila Seal, et al.
Human Molecular Genetics|May 15, 2015
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowthChey Loveday, Katrina Tatton-Brown, Matthew Clarke, et al.
American Journal of Human Genetics|May 6, 2017
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual DisabilityKatrina Tatton-Brown, Chey Loveday, Shawn Yost, et al.
Nature Communications|August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumourSandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Nature Genetics|May 14, 2013
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14Elise Ruark, Sheila Seal, Heather McDonald, et al.
Nature Genetics|May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregationShawn Yost, Bas de Wolf, Sandra Hanks, et al.
Nature Genetics|May 10, 2011
Mutations in CEP57 cause mosaic variegated aneuploidy syndromeKatie Snape, Sandra Hanks, Elise Ruark, et al.
Nature Genetics|March 12, 2014
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disabilityKatrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Breast Cancer Research and Treatment|April 25, 2012
Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancerKatie Snape, Elise Ruark, Patrick Tarpey, et al.
F1000Research|February 3, 2016
The ICR1000 UK exome series: a resource of gene variation in an outbred populationElise Ruark, Márton Münz, Anthony Renwick, et al.
Scientific Reports|July 14, 2016
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patientsAngela George, Daniel Riddell, Sheila Seal, et al.
Human Molecular Genetics|May 15, 2015
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowthChey Loveday, Katrina Tatton-Brown, Matthew Clarke, et al.
American Journal of Human Genetics|May 6, 2017
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual DisabilityKatrina Tatton-Brown, Chey Loveday, Shawn Yost, et al.
Nature Communications|August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumourSandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Nature Genetics|May 14, 2013
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14Elise Ruark, Sheila Seal, Heather McDonald, et al.
Nature Genetics|May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregationShawn Yost, Bas de Wolf, Sandra Hanks, et al.
Nature Genetics|May 10, 2011
Mutations in CEP57 cause mosaic variegated aneuploidy syndromeKatie Snape, Sandra Hanks, Elise Ruark, et al.
Nature Genetics|March 12, 2014
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disabilityKatrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.
Pageof 3