Laryssa A. Huryn

Also affiliated with National Eye Institute

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 33 papers. Top paper: “Intrathecal Gene Therapy for Giant Axonal Neuropathy”.

Intrathecal Gene Therapy for Giant Axonal Neuropathy

New England Journal of Medicine(2024)10.1056/nejmoa2307952

N/A

1.4DataRank · unranked

59 citations

Joshua J. Todd, Dimah Saade, Gina Norato, Minal Jain, Tanya Lehky +24 more

Severity modeling of propionic acidemia using clinical and laboratory biomarkers

Genetics in Medicine(2021)10.1038/s41436-021-01173-2

N/A

0.846DataRank · unranked

23 citations

Irini Manoli, Paul Juneau, Jennifer L. Sloan, Susan Ferry, Jennifer Myles +15 more

GM1 gangliosidosis type II: Results of a 10-year prospective study

Genetics in Medicine(2024)10.1016/j.gim.2024.101144

N/A

0.557DataRank · unranked

19 citations

Cristan Farmer, Jean M. Johnston, Sangwoo T. Han, David Adams, Adam L. Hartman +24 more

Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity

Frontiers in Immunology(2023)10.3389/fimmu.2023.1172004

N/A

0.413DataRank · unranked

8 citations

Morgan N Similuk, Rajarshi Ghosh, Bryce A. Seifert, Leila Jamal, Michael Kamen +31 more

Natural History of Visual Dysfunction in ABCA4 Retinopathy and Its Genetic Correlates

American Journal of Ophthalmology(2023)10.1016/j.ajo.2023.05.014

N/A

0.362DataRank · unranked

8 citations

Laryssa A. Huryn, Marisa Boyle, Catherine A. Cukras, Wadih M. Zein, Amy Turriff +5 more

The qMini assay identifies an overlooked class of splice variants

medRxiv(2023)10.1101/2023.11.02.23297963

N/A

0.104DataRank · unranked

1 citations

Chelsea Bender, Madhulatha Pantrangi, Nia Moore, Melissa Reeves, Amelia Naik +10 more

Reply

Journal of American Association for Pediatric Ophthalmology and Strabismus(2020)10.1016/j.jaapos.2019.10.009

N/A

0DataRank · unranked

0 citations

Catherine A. Cukras, Brian P. Brooks, Laryssa A. Huryn, Amy Turriff

In vivo assessment of neurodegeneration in Spinocerebellar Ataxia type 7

medRxiv(2020)10.1101/2020.10.05.20207340

N/A

0DataRank · unranked

0 citations

Shabbir Hussain I. Merchant, Sanaz Attaripour-Isfahani, Hyun Joo Cho, Patrick Mcgurrin, Brian P. Brooks +5 more

Integrating adaptive optics-SLO and OCT for multimodal visualization of the human retinal pigment epithelial mosaic

Biomedical Optics Express(2021)10.1364/boe.413438

N/A

0DataRank · unranked

45 citations

Tao Liu, Nancy Aguilera, Joanne Li, Jianfei Liu, Rongwen Lu +7 more

Persistent Dark Cones in Oligocone Trichromacy Revealed by Multimodal Adaptive Optics Ophthalmoscopy

Frontiers in Aging Neuroscience(2021)10.3389/fnagi.2021.629214

N/A

0DataRank · unranked

12 citations

Tao Liu, Oliver Flynn, Amy Turriff, Zhuolin Liu, Ehsan Ullah +10 more

In vivo assessment of neurodegeneration in Spinocerebellar Ataxia type 7

NeuroImage Clinical(2021)10.1016/j.nicl.2021.102561

N/A

0DataRank · unranked

6 citations

Shabbir Hussain I. Merchant, Sanaz Attaripour-Isfahani, Hyun Joo Cho, Patrick Mcgurrin, Brian P. Brooks +5 more

Single-cell–resolution map of human retinal pigment epithelium helps discover subpopulations with differential disease sensitivity

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2117553119

N/A

0DataRank · unranked

93 citations

Ruchi Sharma, A. I. Volkov, Arvydas Maminishkis, Nathan Hotaling, Laryssa A. Huryn +5 more

Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

Annals of the Rheumatic Diseases(2022)10.1136/annrheumdis-2022-222629

N/A

0DataRank · unranked

70 citations

Shilpa Kodati, Laryssa A. Huryn, Hongying Wang, Blake M. Warner, Priyam Jani +95 more

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

Ophthalmology(2022)10.1016/j.ophtha.2022.10.026

N/A

0DataRank · unranked

35 citations

Christina Torres Kozycki, Jasmine Y. Serpen, Wadih M. Zein, Ehsan Ullah, Alessandro Iannaccone +8 more

Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome

British Journal of Ophthalmology(2022)10.1136/bjophthalmol-2022-321103

N/A

0DataRank · unranked

23 citations

Taylor Flaherty, Rosalie Nolen, Lev Prasov, Wadih M. Zein, Catherine A. Cukras +8 more

Widespread subclinical cellular changes revealed across a neural-epithelial-vascular complex in choroideremia using adaptive optics

Communications Biology(2022)10.1038/s42003-022-03842-7

N/A

0DataRank · unranked

16 citations

Tao Liu, Andrew J. Bower, Joanne Li, Sarah Abouassali, Rongwen Lu +20 more

Visualization of erythrocyte stasis in the living human eye in health and disease

iScience(2022)10.1016/j.isci.2022.105755

N/A

0DataRank · unranked

6 citations

Dongyi Wang, Jessica Pottenburgh, Andrew J. Bower, Samuel Asanad, Eric W. Lai +7 more

Chromosomal Microarray Analysis Supplements Exome Sequencing to Diagnose Children with Suspected Inborn Errors of Immunity

Research Square(2022)10.21203/rs.3.rs-2211010/v1

N/A

0DataRank · unranked

1 citations

Morgan N Similuk, Rajarshi Ghosh, Bryce A. Seifert, Leila Jamal, Michael Kamen +30 more

Genotype–Phenotype Association in ABCA4-Associated Retinopathy

Advances in experimental medicine and biology(2023)10.1007/978-3-031-27681-1_42

N/A

0DataRank · unranked

6 citations

Wadih M. Zein, Laryssa A. Huryn, Catherine A. Cukras, Brett G. Jeffrey, Robert B. Hufnagel +2 more

Ocular findings in Jansen metaphyseal chondrodysplasia

JBMR Plus(2024)10.1093/jbmrpl/ziae089

N/A

0DataRank · unranked

2 citations

M Teresa Magone De Quadros Costa, Laryssa A. Huryn, Kristen S. Pan, Konstantinia Almpani, Anisha Ninan +8 more

GM1 Gangliosidosis Type II: Results of a 10-Year Prospective Study

medRxiv(2024)10.1101/2024.01.04.24300778

N/A

0DataRank · unranked

5 citations

Cristan Farmer, Jean M. Johnston, Sangwoo T. Han, David R. Adams, Adam L. Hartman +23 more

OUTER RETINAL MICROCAVITATIONS IN RETINITIS PIGMENTOSA

Retina(2024)10.1097/iae.0000000000004091

N/A

0DataRank · unranked

0 citations

Laryssa A. Huryn, Robert B. Hufnagel, Ehsan Ullah, Aime Agather, Delphine Blain +4 more

Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans

Translational Vision Science & Technology(2024)10.1167/tvst.13.9.4

N/A

0DataRank · unranked

0 citations

Raisa Ionin, Laryssa A. Huryn, Catherine A. Cukras, Delphine Blain, Aime Agather +5 more

Artificial intelligence assisted clinical fluorescence imaging achieves in vivo cellular resolution comparable to adaptive optics ophthalmoscopy

Communications Medicine(2025)10.1038/s43856-025-00803-z

N/A

0DataRank · unranked

5 citations

Jianfei Liu, Vineeta Das, Hong Le, Nancy Aguilera, Andrew J. Bower +11 more

Electroretinography With the RM Electrode: Normative Reference Ranges, Variation With Age, and Comparison With the Burian–Allen Electrode

Translational Vision Science & Technology(2025)10.1167/tvst.14.6.13

N/A

0DataRank · unranked

1 citations

Xueyang Yin, Christina Appleman, Sobany Suy, Anna Papadogiannis, Daniel Claus +5 more

Biallelic loss-of-function variants in C19orf44 lead to retinal degeneration

Journal of Medical Genetics(2025)10.1136/jmg-2025-110681

N/A

0DataRank · unranked

1 citations

Meng Wang, Yumei Li, Sabika Firasat, Mark E. Pennesi, Michael B. Gorin +10 more

Defining the clinical phenotype of Saul–Wilson syndrome

Genetics in Medicine(2020)10.1038/s41436-019-0737-1

N/A

0DataRank · unranked

21 citations

Wadih M. Zein, Laryssa A. Huryn, Andrea Merker, Seth Berger, William G. Wilson +26 more

Generation of four human pluripotent stem cell lines harboring OPA1-related optic atrophy variant

Stem Cell Research(2025)10.1016/j.scr.2025.103766

N/A

0DataRank · unranked

0 citations

Sairah Yousaf, Bin Guan, Amelia Naik, Rafael Villasmil, Raymond Oh +5 more

Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61484

N/A

0DataRank · unranked

8 citations

Ehsan Ullah, Amy Turriff, Blake M. Warner, Julie A. Conley, Paul R. Mark +3 more

Ocular and Systemic Findings in Adults with Uveal Coloboma

Ophthalmology(2020)10.1016/j.ophtha.2020.05.028

N/A

0DataRank · unranked

14 citations

Laryssa A. Huryn, Robert B. Hufnagel, Wadih M. Zein, Delphine Blain, Brian P. Brooks +1 more

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

Scientific Reports(2020)10.1038/s41598-020-76725-8

N/A

0DataRank · unranked

36 citations

Bin Guan, Ehsan Ullah, Steven M. Archer, Bernadete Ayres, Cagri G. Besirli +18 more

A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2020)10.1002/ajmg.c.31822

N/A

0DataRank · unranked

28 citations

Malena Daich Varela, Anthony G. Robson, Karen Pierpoint, Rola Ba‐Abbad, Savita Nutan +12 more

The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2020)10.1002/ajmg.c.31823

N/A

0DataRank · unranked

25 citations

Priyam Jani, Wadih M. Zein, Precilla D’Souza, Lynne A. Wolfe, Jennifer Chisholm +6 more