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Morad Ansari

Showing results (1-10 of 35) with videos related to

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BMC Bioinformatics|July 21, 2014
Variant detection sensitivity and biases in whole genome and exome sequencingAlison M Meynert, Morad Ansari, David R FitzPatrick, et al.
Human Molecular Genetics|June 14, 2013
Regional chromatin decompaction in Cornelia de Lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCFLeisha D Nolen, Shelagh Boyle, Morad Ansari, et al.
American Journal of Medical Genetics. Part A|April 21, 2017
Genotype-phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with ageJoanna Moss, Jessica Penhallow, Morad Ansari, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single centerChristina Gerth-Kahlert, Kathleen Williamson, Morad Ansari, et al.
Genome Medicine|November 7, 2024
Curating genomic disease-gene relationships with Gene2Phenotype (G2P)T Michael Yates, Morad Ansari, Louise Thompson, et al.
The European Journal of Health Economics : HEPAC : Health Economics in Prevention and Care|September 9, 2024
Should Scotland provide genome-wide sequencing for the diagnosis of rare developmental disorders? A cost-effectiveness analysisMichael Abbott, Mandy Ryan, Rodolfo Hernández, et al.
European Journal of Medical Genetics|September 8, 2014
A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAXMorad Ansari, Jacqueline K Rainger, Jennie E Murray, et al.
Journal of Neurology|June 9, 2024
Genotypes and phenotypes of motor neuron disease: an update of the genetic landscape in ScotlandDanielle J Leighton, Morad Ansari, Judith Newton, et al.
Nature Genetics|January 31, 2018
BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndromeGabrielle Olley, Morad Ansari, Hemant Bengani, et al.
Nature Genetics|February 15, 2018
Publisher Correction: BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndromeGabrielle Olley, Morad Ansari, Hemant Bengani, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
BMC Bioinformatics|July 21, 2014
Variant detection sensitivity and biases in whole genome and exome sequencingAlison M Meynert, Morad Ansari, David R FitzPatrick, et al.
Human Molecular Genetics|June 14, 2013
Regional chromatin decompaction in Cornelia de Lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCFLeisha D Nolen, Shelagh Boyle, Morad Ansari, et al.
American Journal of Medical Genetics. Part A|April 21, 2017
Genotype-phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with ageJoanna Moss, Jessica Penhallow, Morad Ansari, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single centerChristina Gerth-Kahlert, Kathleen Williamson, Morad Ansari, et al.
Genome Medicine|November 7, 2024
Curating genomic disease-gene relationships with Gene2Phenotype (G2P)T Michael Yates, Morad Ansari, Louise Thompson, et al.
The European Journal of Health Economics : HEPAC : Health Economics in Prevention and Care|September 9, 2024
Should Scotland provide genome-wide sequencing for the diagnosis of rare developmental disorders? A cost-effectiveness analysisMichael Abbott, Mandy Ryan, Rodolfo Hernández, et al.
European Journal of Medical Genetics|September 8, 2014
A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAXMorad Ansari, Jacqueline K Rainger, Jennie E Murray, et al.
Journal of Neurology|June 9, 2024
Genotypes and phenotypes of motor neuron disease: an update of the genetic landscape in ScotlandDanielle J Leighton, Morad Ansari, Judith Newton, et al.
Nature Genetics|January 31, 2018
BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndromeGabrielle Olley, Morad Ansari, Hemant Bengani, et al.
Nature Genetics|February 15, 2018
Publisher Correction: BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndromeGabrielle Olley, Morad Ansari, Hemant Bengani, et al.
Pageof 4