Brian P Brooks

Years Active: 2020-2022
Publications (10 Years): 4

This page only lists publications with an associated author ORCID identifier.

Publications

Jana Zernant, Winston Lee, Jun Wang, Kerry Goetz, Ehsan Ullah, Takayuki Nagasaki, Pei-Yin Su, Gerald A Fishman, Stephen H Tsang, Santa J Tumminia, Brian P Brooks, Robert B Hufnagel, Rui Chen, Rando Allikmets
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease. PLoS genetics 18 (3) (2022)
Malena Daich Varela, Robert B Hufnagel, Bin Guan, Delphine Blain, Julie C Sapp, Andrea L Gropman, Ramakrishna Alur, Jennifer J Johnston, Leslie G Biesecker, Brian P Brooks
Clinical diagnosis of presumed SOX2 gonadosomatic mosaicism. Ophthalmic genetics 42 (3) (2021)
Julia Chertkof, Robert B Hufnagel, Delphine Blain, Andrea L Gropman, Brian P Brooks
Retinoschisis associated with Kearns-Sayre syndrome. Ophthalmic genetics 41 (5) (2020)
Rosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, Amy E Turriff, Carmen C Brewer, Christopher K Zalewski, Kelly A King, Talah T Wafa, Andrew J Griffith, Brian P Brooks, Wadih M Zein
Atypical and ultra-rare Usher syndrome: a review. Ophthalmic genetics 41 (5) (2020)

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