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Scott A Melville

Showing results (1-10 of 9) with videos related to

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Genomics|July 22, 2005
A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogsScott A Melville, Carmen L Wilson, Chiu S Chiang, et al.
Annals of Neurology|June 30, 2012
Multiple loci influencing hippocampal degeneration identified by genome scanScott A Melville, Jacqueline Buros, Antonio R Parrado, et al.
American Journal of Medical Genetics. Part A|September 11, 2025
Long-Read Sequencing of a Neurodevelopmental Disorder Patient Reveals Complex Rearrangement Involving the ARID1B GeneTam P Sneddon, Scott A Melville, Mai Xiong, et al.
Journal of Clinical and Translational Science|April 10, 2026
Expanding access to genomic analysis and reporting in research studies: The GENYSIS research coreKimberly S Foss, Tam P Sneddon, Eleanor P Fensterle, et al.
Human Molecular Genetics|January 29, 2011
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene clusterFabiola Del Greco M, Cristian Pattaro, Andreas Luchner, et al.
Human Molecular Genetics|January 7, 2011
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levelsIrene Pichler, Cosetta Minelli, Serena Sanna, et al.
BMC Medical Genetics|March 13, 2010
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine levelCristian Pattaro, Alessandro De Grandi, Veronique Vitart, et al.
European Journal of Human Genetics : EJHG|May 5, 2016
Genetic variants in RBFOX3 are associated with sleep latencyNajaf Amin, Karla V Allebrandt, Ashley van der Spek, et al.
Nature Human Behaviour|September 29, 2020
Genome-wide association study identifies 48 common genetic variants associated with handednessGabriel Cuellar-Partida, Joyce Y Tung, Nicholas Eriksson, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Genomics|July 22, 2005
A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogsScott A Melville, Carmen L Wilson, Chiu S Chiang, et al.
Annals of Neurology|June 30, 2012
Multiple loci influencing hippocampal degeneration identified by genome scanScott A Melville, Jacqueline Buros, Antonio R Parrado, et al.
American Journal of Medical Genetics. Part A|September 11, 2025
Long-Read Sequencing of a Neurodevelopmental Disorder Patient Reveals Complex Rearrangement Involving the ARID1B GeneTam P Sneddon, Scott A Melville, Mai Xiong, et al.
Journal of Clinical and Translational Science|April 10, 2026
Expanding access to genomic analysis and reporting in research studies: The GENYSIS research coreKimberly S Foss, Tam P Sneddon, Eleanor P Fensterle, et al.
Human Molecular Genetics|January 29, 2011
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene clusterFabiola Del Greco M, Cristian Pattaro, Andreas Luchner, et al.
Human Molecular Genetics|January 7, 2011
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levelsIrene Pichler, Cosetta Minelli, Serena Sanna, et al.
BMC Medical Genetics|March 13, 2010
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine levelCristian Pattaro, Alessandro De Grandi, Veronique Vitart, et al.
European Journal of Human Genetics : EJHG|May 5, 2016
Genetic variants in RBFOX3 are associated with sleep latencyNajaf Amin, Karla V Allebrandt, Ashley van der Spek, et al.
Nature Human Behaviour|September 29, 2020
Genome-wide association study identifies 48 common genetic variants associated with handednessGabriel Cuellar-Partida, Joyce Y Tung, Nicholas Eriksson, et al.
Pageof 1