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David L Bennett

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Science Advances|April 16, 2025

Permissive central tolerance plus defective peripheral checkpoints license pathogenic memory B cells in CASPR2-antibody encephalitisBo Sun, Dominique Fernandes, John Soltys, et al.

Pain|October 29, 2024

Genetic associations of neuropathic pain and sensory profile in a deeply phenotyped neuropathy cohortMikael Åkerlund, Georgios Baskozos, Wenqianglong Li, et al.

Science (New York, N.Y.)|May 25, 2019

Germline selection shapes human mitochondrial DNA diversityWei Wei, Salih Tuna, Michael J Keogh, et al.

Nature|June 26, 2020

Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.

Brain : a Journal of Neurology|September 28, 2023

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathiesAnnette Lischka, Katja Eggermann, Christopher J Record, et al.

Genome Medicine|November 10, 2023

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.

Pageof 10

Search research articles

Showing results (91-100 of 96) with videos related to

Sort By:

Pageof 10

You have reached the last page of results.This site can display upto 96 results.

Science Advances|April 16, 2025

Permissive central tolerance plus defective peripheral checkpoints license pathogenic memory B cells in CASPR2-antibody encephalitisBo Sun, Dominique Fernandes, John Soltys, et al.

Pain|October 29, 2024

Genetic associations of neuropathic pain and sensory profile in a deeply phenotyped neuropathy cohortMikael Åkerlund, Georgios Baskozos, Wenqianglong Li, et al.

Science (New York, N.Y.)|May 25, 2019

Germline selection shapes human mitochondrial DNA diversityWei Wei, Salih Tuna, Michael J Keogh, et al.

Nature|June 26, 2020

Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.

Brain : a Journal of Neurology|September 28, 2023

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathiesAnnette Lischka, Katja Eggermann, Christopher J Record, et al.

Genome Medicine|November 10, 2023

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.

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