Brian P Brooks

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 10

Top Topics

Cataract Surgery

Optical Coherence Tomography

Top Venues

Ophthalmic genetics

Ophthalmic epidemiology

The British journal of ophthalmology

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

Publications

Emile R Vieta-Ferrer, Ehsan Ullah, Delphine Blain, Julie A Christensen, Carmen C Brewer, James E Balow, Aman George, Robert B Hufnagel, Tiziana Cogliati, Brian P Brooks
A novel variant affecting the cytoplasmic tail of the FAT1 protocadherin causing coloboma and renal failure: A case report. Ophthalmic genetics 44 (2) (2023)
Emile R Vieta-Ferrer, Ehsan Ullah, Delphine Blain, Julie A Christensen, Carmen C Brewer, James E Balow, Aman George, Robert B Hufnagel, Tiziana Cogliati, Brian P Brooks
A novel variant affecting the cytoplasmic tail of the FAT1 protocadherin causing coloboma and renal failure: A case report. Ophthalmic genetics 44 (2) (2023)
Charles DeYoung, Bin Guan, Ehsan Ullah, Delphine Blain, Robert B Hufnagel, Brian P Brooks
De novo frameshift mutation in YAP1 associated with bilateral uveal coloboma and microphthalmia. Ophthalmic genetics 43 (4) (2022)
Aman George, Jerry Lee, James Liu, Suzie Kim, Brian P Brooks
Zebrafish model of RERE syndrome recapitulates key ophthalmic defects that are rescued by small molecule inhibitor of shh signaling. Developmental dynamics : an official publication of the American Association of Anatomists (2022)
Laryssa A Huryn, Taylor Flaherty, Rosalie Nolen, Lev Prasov, Wadih M Zein, Catherine A Cukras, Sharon Osgood, Neelam Raja, Mark D Levin, Susan Vitale, Brian P Brooks, Robert B Hufnagel, Beth A Kozel
Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome. The British journal of ophthalmology (2022)
Natario L Couser, Brian P Brooks, Arlene V Drack, Suma P Shankar
The evolving role of genetics in ophthalmology. Ophthalmic genetics 42 (2) (2021)
Julia Chertkof, Robert B Hufnagel, Delphine Blain, Andrea L Gropman, Brian P Brooks
Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome". Ophthalmic genetics 42 (1) (2020)
Jeremy M Schraw, Renata H Benjamin, Daryl A Scott, Brian P Brooks, Robert B Hufnagel, Scott D McLean, Hope Northrup, Peter H Langlois, Mark A Canfield, Angela E Scheuerle, Christian P Schaaf, Joseph W Ray, Han Chen, Michael D Swartz, Laura E Mitchell, A J Agopian, Philip J Lupo
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or Microphthalmia. Ophthalmic epidemiology 28 (5) (2020)
Chenchen Niu, Thazha P Prakash, Aneeza Kim, John L Quach, Laryssa A Huryn, Yuechen Yang, Edith Lopez, Ali Jazayeri, Gene Hung, Bryce L Sopher, Brian P Brooks, Eric E Swayze, C Frank Bennett, Albert R La Spada
Antisense oligonucleotides targeting mutant Ataxin-7 restore visual function in a mouse model of spinocerebellar ataxia type 7. Science translational medicine 10 (465) (2019)
Vijay K Kalaskar, Ramakrishna P Alur, LeeAnn K Li, James W Thomas, Yuri V Sergeev, Delphine Blain, Robert B Hufnagel, Tiziana Cogliati, Brian P Brooks
High-throughput custom capture sequencing identifies novel mutations in coloboma-associated genes: Mutation in DNA-binding domain of retinoic acid receptor beta affects nuclear localization causing ocular coloboma. Human mutation 41 (3) (2019)