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Michael A Simpson

Showing results (41-50 of 168) with videos related to

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Neurogenetics|February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegiaJohanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
The Journal of Investigative Dermatology|May 25, 2012
Mutations in the γ-secretase genes NCSTN, PSENEN, and PSEN1 underlie rare forms of hidradenitis suppurativa (acne inversa)Andrew E Pink, Michael A Simpson, Nemesha Desai, et al.
The Journal of Investigative Dermatology|March 18, 2011
PSENEN and NCSTN mutations in familial hidradenitis suppurativa (Acne Inversa)Andrew E Pink, Michael A Simpson, Glen W Brice, et al.
Behavior Genetics|March 23, 2010
A three-stage genome-wide association study of general cognitive ability: hunting the small effectsOliver S P Davis, Lee M Butcher, Sophia J Docherty, et al.
Skin Health and Disease|November 28, 2025
Unravelling the causal link between gut microbiota and acne risk using a genetic approachFangyuan Cao, Natalia S Ogonowski, Santiago Díaz-Torres, et al.
The Journal of Investigative Dermatology|May 27, 2025
Investigating the Genetic Basis of the Influence of Adiposity on Psoriasis: A Cross-Sectional Study in a Large United Kingdom Population-Based BiobankRavi Ramessur, Jake Saklatvala, Mari Løset, et al.
The Journal of Investigative Dermatology|June 29, 2016
Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic IchthyosisTakuya Takeichi, Lu Liu, Alya Abdul-Wahab, et al.
Skin Health and Disease|May 14, 2025
The role of lipid metabolism in acne risk: integrating blood metabolite and genetic insightsMingjuan Liu, Santiago Diaz-Torres, Brittany L Mitchell, et al.
The Journal of Investigative Dermatology|March 4, 2023
Genetic Validation of Psoriasis Phenotyping in UK Biobank Supports the Utility of Self-Reported Data and Composite Definitions for Large Genetic and Epidemiological StudiesJake R Saklatvala, Ken B Hanscombe, Satveer K Mahil, et al.
British Journal of Haematology|March 30, 2019
Novel ADA2 mutation presenting with neutropenia, lymphopenia and bone marrow failure in patients with deficiency in adenosine deaminase 2 (DADA2)Rohit R Ghurye, Kruthika Sundaram, Frances Smith, et al.
Pageof 17

Showing results (41-50 of 168) with videos related to

Sort By:
Pageof 17
Neurogenetics|February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegiaJohanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
The Journal of Investigative Dermatology|May 25, 2012
Mutations in the γ-secretase genes NCSTN, PSENEN, and PSEN1 underlie rare forms of hidradenitis suppurativa (acne inversa)Andrew E Pink, Michael A Simpson, Nemesha Desai, et al.
The Journal of Investigative Dermatology|March 18, 2011
PSENEN and NCSTN mutations in familial hidradenitis suppurativa (Acne Inversa)Andrew E Pink, Michael A Simpson, Glen W Brice, et al.
Behavior Genetics|March 23, 2010
A three-stage genome-wide association study of general cognitive ability: hunting the small effectsOliver S P Davis, Lee M Butcher, Sophia J Docherty, et al.
Skin Health and Disease|November 28, 2025
Unravelling the causal link between gut microbiota and acne risk using a genetic approachFangyuan Cao, Natalia S Ogonowski, Santiago Díaz-Torres, et al.
The Journal of Investigative Dermatology|May 27, 2025
Investigating the Genetic Basis of the Influence of Adiposity on Psoriasis: A Cross-Sectional Study in a Large United Kingdom Population-Based BiobankRavi Ramessur, Jake Saklatvala, Mari Løset, et al.
The Journal of Investigative Dermatology|June 29, 2016
Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic IchthyosisTakuya Takeichi, Lu Liu, Alya Abdul-Wahab, et al.
Skin Health and Disease|May 14, 2025
The role of lipid metabolism in acne risk: integrating blood metabolite and genetic insightsMingjuan Liu, Santiago Diaz-Torres, Brittany L Mitchell, et al.
The Journal of Investigative Dermatology|March 4, 2023
Genetic Validation of Psoriasis Phenotyping in UK Biobank Supports the Utility of Self-Reported Data and Composite Definitions for Large Genetic and Epidemiological StudiesJake R Saklatvala, Ken B Hanscombe, Satveer K Mahil, et al.
British Journal of Haematology|March 30, 2019
Novel ADA2 mutation presenting with neutropenia, lymphopenia and bone marrow failure in patients with deficiency in adenosine deaminase 2 (DADA2)Rohit R Ghurye, Kruthika Sundaram, Frances Smith, et al.
Pageof 17