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Michael A Simpson

Showing results (31-40 of 168) with videos related to

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The Journal of Dermatology|August 14, 2020
Blaschko-linear lichen planus: Clinicopathological and genetic analysisMati Chuamanochan, Alexandros Onoufriadis, Shahir Farnood, et al.
Intelligence|January 17, 2015
Thinking positively: The genetics of high intelligenceNicholas G Shakeshaft, Maciej Trzaskowski, Andrew McMillan, et al.
Blood|June 27, 2018
Mutation in <i>GNE</i> is associated with severe congenital thrombocytopeniaJane Futterer, Amanda Dalby, Gillian C Lowe, et al.
The Journal of Investigative Dermatology|January 2, 2025
GWAS Meta-Analysis Identifies Susceptibility Loci for Keloids and Hypertrophic Scarring in EuropeansNick Dand, Chuin Y Ung, Jake R Saklatvala, et al.
Cytogenetic and Genome Research|November 8, 2020
New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform DermatitisIncilay Kalay Yildizhan, Ezgi Gökpınar İli, Alexandros Onoufriadis, et al.
European Journal of Medical Genetics|November 13, 2012
Acrocallosal syndrome: identification of a novel KIF7 mutation and evidence for oligogenic inheritanceDiana M Walsh, Stavit A Shalev, Michael A Simpson, et al.
JAMA Dermatology|May 29, 2024
Gene-Environment Interaction Between CYP1B1 and Oral Contraception on Frontal Fibrosing AlopeciaTuntas Rayinda, Sheila M McSweeney, Evangelos Christou, et al.
American Journal of Medical Genetics. Part A|September 9, 2017
Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45Rachel Straussberg, Alexandros Onoufriadis, Osnat Konen, et al.
Scientific Reports|January 25, 2017
Fine mapping genetic associations between the HLA region and extremely high intelligenceDelilah Zabaneh, Eva Krapohl, Michael A Simpson, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney syndromeMary J Gray, Chong Ae Kim, Debora Romeo Bertola, et al.
Pageof 17

Showing results (31-40 of 168) with videos related to

Sort By:
Pageof 17
The Journal of Dermatology|August 14, 2020
Blaschko-linear lichen planus: Clinicopathological and genetic analysisMati Chuamanochan, Alexandros Onoufriadis, Shahir Farnood, et al.
Intelligence|January 17, 2015
Thinking positively: The genetics of high intelligenceNicholas G Shakeshaft, Maciej Trzaskowski, Andrew McMillan, et al.
Blood|June 27, 2018
Mutation in <i>GNE</i> is associated with severe congenital thrombocytopeniaJane Futterer, Amanda Dalby, Gillian C Lowe, et al.
The Journal of Investigative Dermatology|January 2, 2025
GWAS Meta-Analysis Identifies Susceptibility Loci for Keloids and Hypertrophic Scarring in EuropeansNick Dand, Chuin Y Ung, Jake R Saklatvala, et al.
Cytogenetic and Genome Research|November 8, 2020
New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform DermatitisIncilay Kalay Yildizhan, Ezgi Gökpınar İli, Alexandros Onoufriadis, et al.
European Journal of Medical Genetics|November 13, 2012
Acrocallosal syndrome: identification of a novel KIF7 mutation and evidence for oligogenic inheritanceDiana M Walsh, Stavit A Shalev, Michael A Simpson, et al.
JAMA Dermatology|May 29, 2024
Gene-Environment Interaction Between CYP1B1 and Oral Contraception on Frontal Fibrosing AlopeciaTuntas Rayinda, Sheila M McSweeney, Evangelos Christou, et al.
American Journal of Medical Genetics. Part A|September 9, 2017
Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45Rachel Straussberg, Alexandros Onoufriadis, Osnat Konen, et al.
Scientific Reports|January 25, 2017
Fine mapping genetic associations between the HLA region and extremely high intelligenceDelilah Zabaneh, Eva Krapohl, Michael A Simpson, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney syndromeMary J Gray, Chong Ae Kim, Debora Romeo Bertola, et al.
Pageof 17