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McVean

Showing results (201-210 of 234) with videos related to

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Nature Communications|July 29, 2022
Mouse fetal growth restriction through parental and fetal immune gene variation and intercellular communications cascadeGurman Kaur, Caroline B M Porter, Orr Ashenberg, et al.
Nature Genetics|November 6, 2021
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disordersChris Eijsbouts, Tenghao Zheng, Nicholas A Kennedy, et al.
Human Molecular Genetics|October 11, 2017
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disabilityBenjamin Davies, Laurence A Brown, Ondrej Cais, et al.
Diabetes Technology & Therapeutics|October 2, 2023
Safety and Glycemic Outcomes During the MiniMed<sup>TM</sup> Advanced Hybrid Closed-Loop System Pivotal Trial in Children and Adolescents with Type 1 DiabetesCatherine Pihoker, Dorothy I Shulman, Gregory P Forlenza, et al.
Nature Communications|December 22, 2015
Rapid antibiotic-resistance predictions from genome sequence data for Staphylococcus aureus and Mycobacterium tuberculosisPhelim Bradley, N Claire Gordon, Timothy M Walker, et al.
Nature Communications|November 7, 2014
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variantsKalliope Panoutsopoulou, Konstantinos Hatzikotoulas, Dionysia Kiara Xifara, et al.
Plos Genetics|December 14, 2012
Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor developmentStefano Lise, Yvonne Clarkson, Emma Perkins, et al.
Nature Genetics|September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCPaul I W de Bakker, Gil McVean, Pardis C Sabeti, et al.
Human Molecular Genetics|January 28, 2014
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosisHilary C Martin, Grace E Kim, Alistair T Pagnamenta, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2009
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases, John D Rioux, Philippe Goyette, et al.
Pageof 24

Showing results (201-210 of 234) with videos related to

Sort By:
Pageof 24
Nature Communications|July 29, 2022
Mouse fetal growth restriction through parental and fetal immune gene variation and intercellular communications cascadeGurman Kaur, Caroline B M Porter, Orr Ashenberg, et al.
Nature Genetics|November 6, 2021
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disordersChris Eijsbouts, Tenghao Zheng, Nicholas A Kennedy, et al.
Human Molecular Genetics|October 11, 2017
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disabilityBenjamin Davies, Laurence A Brown, Ondrej Cais, et al.
Diabetes Technology & Therapeutics|October 2, 2023
Safety and Glycemic Outcomes During the MiniMed<sup>TM</sup> Advanced Hybrid Closed-Loop System Pivotal Trial in Children and Adolescents with Type 1 DiabetesCatherine Pihoker, Dorothy I Shulman, Gregory P Forlenza, et al.
Nature Communications|December 22, 2015
Rapid antibiotic-resistance predictions from genome sequence data for Staphylococcus aureus and Mycobacterium tuberculosisPhelim Bradley, N Claire Gordon, Timothy M Walker, et al.
Nature Communications|November 7, 2014
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variantsKalliope Panoutsopoulou, Konstantinos Hatzikotoulas, Dionysia Kiara Xifara, et al.
Plos Genetics|December 14, 2012
Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor developmentStefano Lise, Yvonne Clarkson, Emma Perkins, et al.
Nature Genetics|September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCPaul I W de Bakker, Gil McVean, Pardis C Sabeti, et al.
Human Molecular Genetics|January 28, 2014
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosisHilary C Martin, Grace E Kim, Alistair T Pagnamenta, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2009
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases, John D Rioux, Philippe Goyette, et al.
Pageof 24