Immunogenetics of the Ocular Anterior Segment: Lessons from Inherited Disorders

por Serpen, Jasmine Y., Armenti, Stephen T., Prasov, Lev
Publicado 2021

1000 human genomes carry widespread signatures of GC biased gene conversion

por Dutta, Rajib, Saha-Mandal, Arnab, Cheng, Xi, Qiu, Shuhao, Serpen, Jasmine, Fedorova, Larisa, Fedorov, Alexei
Publicado 2018

A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification

por Serpen, Jasmine Y., Presley, William, Beil, Adelyn, Armenti, Stephen T., Johnson, Kayla, Mian, Shahzad I., Innis, Jeffrey W., Prasov, Lev
Publicado 2023

Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort

por Serpen, Jasmine Y., Prasov, Lev, Zein, Wadih M., Cukras, Catherine A., Cunningham, Denise, Murphy, Elizabeth C., Turriff, Amy, Brooks, Brian P., Huryn, Laryssa A.
Publicado 2020

Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF κB–Mediated Autoinflammatory Disease wit...

por Huryn, Laryssa A., Kozycki, Christina Torres, Serpen, Jasmine Y., Zein, Wadih M., Ullah, Ehsan, Iannaccone, Alessandro, Williams, Lloyd B., Sobrin, Lucia, Brooks, Brian P., Sen, H. Nida, Hufnagel, Robert B., Kastner, Daniel L., Kodati, Shilpa
Publicado 2023

Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort

por Prasov, Lev, Guan, Bin, Ullah, Ehsan, Archer, Steven M., Ayres, Bernadete M., Besirli, Cagri G., Wiinikka-Buesser, Laurel, Comer, Grant M., Del Monte, Monte A., Elner, Susan G., Garnai, Sarah J., Huryn, Laryssa A., Johnson, Kayla, Kamat, Shivani S., Lieu, Philip, Mian, Shahzad I., Rygiel, Christine A., Serpen, Jasmine Y., Pawar, Hemant S., Brooks, Brian P., Moroi, Sayoko E., Richards, Julia E., Hufnagel, Robert B.
Publicado 2020