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Michael Simpson

Showing results (61-70 of 67) with videos related to

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Kidney International|January 25, 2017
Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease managementAgnieszka Bierzynska, Hugh J McCarthy, Katrina Soderquest, et al.
Plos Genetics|April 28, 2020
Mutations in SPATA13/ASEF2 cause primary angle closure glaucomaNaushin H Waseem, Sancy Low, Amna Z Shah, et al.
The Journal of Allergy and Clinical Immunology|May 30, 2024
A genome-wide meta-analysis of palmoplantar pustulosis implicates T<sub>H</sub>2 responses and cigarette smoking in disease pathogenesisAriana Hernandez-Cordero, Laurent Thomas, Alice Smail, et al.
The Journal of Investigative Dermatology|May 21, 2023
Shared Genetic Risk Variants in Both Male and Female Frontal Fibrosing AlopeciaTuntas Rayinda, Sheila M McSweeney, David Fenton, et al.
Medrxiv : the Preprint Server for Health Sciences|August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodelingAtlas Khan, Poppy A Gould, Yiming Luo, et al.
Science Translational Medicine|May 5, 2017
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosisBradley N Smith, Simon D Topp, Claudia Fallini, et al.
Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Kidney International|January 25, 2017
Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease managementAgnieszka Bierzynska, Hugh J McCarthy, Katrina Soderquest, et al.
Plos Genetics|April 28, 2020
Mutations in SPATA13/ASEF2 cause primary angle closure glaucomaNaushin H Waseem, Sancy Low, Amna Z Shah, et al.
The Journal of Allergy and Clinical Immunology|May 30, 2024
A genome-wide meta-analysis of palmoplantar pustulosis implicates T<sub>H</sub>2 responses and cigarette smoking in disease pathogenesisAriana Hernandez-Cordero, Laurent Thomas, Alice Smail, et al.
The Journal of Investigative Dermatology|May 21, 2023
Shared Genetic Risk Variants in Both Male and Female Frontal Fibrosing AlopeciaTuntas Rayinda, Sheila M McSweeney, David Fenton, et al.
Medrxiv : the Preprint Server for Health Sciences|August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodelingAtlas Khan, Poppy A Gould, Yiming Luo, et al.
Science Translational Medicine|May 5, 2017
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosisBradley N Smith, Simon D Topp, Claudia Fallini, et al.
Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Pageof 7