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David J Cutler

Showing results (31-40 of 142) with videos related to

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Plos One|December 2, 2011
The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registryThomas S Wingo, David J Cutler, Nicole Yarab, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 9, 2004
Aberrant gating of photic input to the suprachiasmatic circadian pacemaker of mice lacking the VPAC2 receptorAlun T Hughes, Briana Fahey, David J Cutler, et al.
Genome Biology|April 5, 2008
Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarraysShin Lin, Benilton Carvalho, David J Cutler, et al.
BMC Medical Genomics|June 10, 2021
Sex-specific recombination patterns predict parent of origin for recurrent genomic disordersTrenell J Mosley, H Richard Johnston, David J Cutler, et al.
Genome Biology|February 8, 2018
Bystro: rapid online variant annotation and natural-language filtering at whole-genome scaleAlex V Kotlar, Cristina E Trevino, Michael E Zwick, et al.
American Journal of Human Genetics|June 14, 2025
CADET: Enhanced transcriptome-wide association analyses in admixed samples using eQTL summary dataS Taylor Head, Qile Dai, Joellen Schildkraut, et al.
American Journal of Human Genetics|November 6, 2020
Not All Autism Genes Are Created Equal: A Response to Myers et alJoseph D Buxbaum, David J Cutler, Mark J Daly, et al.
The Journal of Molecular Diagnostics : JMD|August 26, 2006
An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genomeShaoyu Zhou, Keyaunoosh Kassauei, David J Cutler, et al.
Applied Spectroscopy|July 11, 2009
Simultaneous neutron scattering and Raman scatteringMark A Adams, Stewart F Parker, Felix Fernandez-Alonso, et al.
Molecular Autism|October 2, 2012
Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorderKaryn Meltz Steinberg, Dhanya Ramachandran, Viren C Patel, et al.
Pageof 15

Showing results (31-40 of 142) with videos related to

Sort By:
Pageof 15
Plos One|December 2, 2011
The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registryThomas S Wingo, David J Cutler, Nicole Yarab, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 9, 2004
Aberrant gating of photic input to the suprachiasmatic circadian pacemaker of mice lacking the VPAC2 receptorAlun T Hughes, Briana Fahey, David J Cutler, et al.
Genome Biology|April 5, 2008
Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarraysShin Lin, Benilton Carvalho, David J Cutler, et al.
BMC Medical Genomics|June 10, 2021
Sex-specific recombination patterns predict parent of origin for recurrent genomic disordersTrenell J Mosley, H Richard Johnston, David J Cutler, et al.
Genome Biology|February 8, 2018
Bystro: rapid online variant annotation and natural-language filtering at whole-genome scaleAlex V Kotlar, Cristina E Trevino, Michael E Zwick, et al.
American Journal of Human Genetics|June 14, 2025
CADET: Enhanced transcriptome-wide association analyses in admixed samples using eQTL summary dataS Taylor Head, Qile Dai, Joellen Schildkraut, et al.
American Journal of Human Genetics|November 6, 2020
Not All Autism Genes Are Created Equal: A Response to Myers et alJoseph D Buxbaum, David J Cutler, Mark J Daly, et al.
The Journal of Molecular Diagnostics : JMD|August 26, 2006
An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genomeShaoyu Zhou, Keyaunoosh Kassauei, David J Cutler, et al.
Applied Spectroscopy|July 11, 2009
Simultaneous neutron scattering and Raman scatteringMark A Adams, Stewart F Parker, Felix Fernandez-Alonso, et al.
Molecular Autism|October 2, 2012
Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorderKaryn Meltz Steinberg, Dhanya Ramachandran, Viren C Patel, et al.
Pageof 15