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Alison J Coffey

Showing results (21-30 of 39) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Human Genetics|November 8, 2011
Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing dataMin Hu, Qasim Ayub, José Afonso Guerra-Assunção, et al.
European Journal of Human Genetics : EJHG|April 2, 2024
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsySamin A Sajan, Ralph Gradisch, Florian D Vogel, et al.
Brain : a Journal of Neurology|March 23, 2013
A genetic study of Wilson's disease in the United KingdomAlison J Coffey, Miranda Durkie, Stephen Hague, et al.
Plos Genetics|December 17, 2009
Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxinMelissa K Boles, Bonney M Wilkinson, Laurens G Wilming, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genetics in Medicine Open|January 19, 2026
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genomics|February 6, 2002
Physical and transcript map of the hereditary prostate cancer region at xq27Dietrich A Stephan, Gareth R Howell, Tanya M Teslovich, et al.
Plos One|May 12, 2011
Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorderRené A W Frank, Allan F McRae, Andrew J Pocklington, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Human Genetics|November 8, 2011
Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing dataMin Hu, Qasim Ayub, José Afonso Guerra-Assunção, et al.
European Journal of Human Genetics : EJHG|April 2, 2024
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsySamin A Sajan, Ralph Gradisch, Florian D Vogel, et al.
Brain : a Journal of Neurology|March 23, 2013
A genetic study of Wilson's disease in the United KingdomAlison J Coffey, Miranda Durkie, Stephen Hague, et al.
Plos Genetics|December 17, 2009
Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxinMelissa K Boles, Bonney M Wilkinson, Laurens G Wilming, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genetics in Medicine Open|January 19, 2026
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genomics|February 6, 2002
Physical and transcript map of the hereditary prostate cancer region at xq27Dietrich A Stephan, Gareth R Howell, Tanya M Teslovich, et al.
Plos One|May 12, 2011
Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorderRené A W Frank, Allan F McRae, Andrew J Pocklington, et al.
Pageof 4