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Timothy J Sullivan

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The British Journal of Ophthalmology|January 14, 2026

Orbital inflammation in VEXAS syndromeClare Quigley, James Pietris, Terence Ang, et al.

Investigative Ophthalmology & Visual Science|June 30, 2004

Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)Koki Yamada, Wai-Man Chan, Caroline Andrews, et al.

Nature Genetics|April 22, 2014

Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylationAndrew A Lane, Bjoern Chapuy, Charles Y Lin, et al.

Science (New York, N.Y.)|May 9, 2015

Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.

Pageof 15

Search research articles

Showing results (141-150 of 144) with videos related to

Sort By:

Pageof 15

You have reached the last page of results.This site can display upto 144 results.

The British Journal of Ophthalmology|January 14, 2026

Orbital inflammation in VEXAS syndromeClare Quigley, James Pietris, Terence Ang, et al.

Investigative Ophthalmology & Visual Science|June 30, 2004

Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)Koki Yamada, Wai-Man Chan, Caroline Andrews, et al.

Nature Genetics|April 22, 2014

Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylationAndrew A Lane, Bjoern Chapuy, Charles Y Lin, et al.

Science (New York, N.Y.)|May 9, 2015

Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.

Pageof 15