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Shuwei Li

Showing results (281-290 of 286) with videos related to

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Neuron|November 12, 2024
Potassium ion channel modulation at cancer-neural interface enhances neuronal excitability in epileptogenic glioblastoma multiformeYe Zhang, Wei Duan, Lingchao Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2016
Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Cell Genomics|June 30, 2023
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs target discovery in ankylosing spondylitisAndrew C Brown, Carla J Cohen, Olga Mielczarek, et al.
Human Mutation|October 13, 2018
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variantsKristy Lee, Kate Krempely, Maegan E Roberts, et al.
Nature Communications|April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Pageof 29

Showing results (281-290 of 286) with videos related to

Sort By:
Pageof 29
You have reached the last page of results.This site can display upto 286 results.
Neuron|November 12, 2024
Potassium ion channel modulation at cancer-neural interface enhances neuronal excitability in epileptogenic glioblastoma multiformeYe Zhang, Wei Duan, Lingchao Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2016
Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Cell Genomics|June 30, 2023
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs target discovery in ankylosing spondylitisAndrew C Brown, Carla J Cohen, Olga Mielczarek, et al.
Human Mutation|October 13, 2018
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variantsKristy Lee, Kate Krempely, Maegan E Roberts, et al.
Nature Communications|April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Pageof 29