Wadih M. Zein

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 3%percentile

1.7Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort

Human Mutation(2020)10.1002/humu.24065

Top 13%

1.7DataRank

Top 13%41 citations

Kerry Goetz, Bin Guan, Ehsan Ullah, Delphine Blain, Wadih M. Zein +3 more

Papers

Driven by 38 papers — median percentile 87. Top paper: “Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort”.

Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort

Human Mutation(2020)10.1002/humu.24065

Top 13%

1.7DataRank

Top 13%41 citations

Kerry Goetz, Bin Guan, Ehsan Ullah, Delphine Blain, Wadih M. Zein +3 more

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

Atypical and ultra-rare Usher syndrome: a review

Ophthalmic Genetics(2020)10.1080/13816810.2020.1747090

N/A

0.538DataRank · unranked

35 citations

Robert B. Hufnagel, Thomas B. Friedman, Amy Turriff, Carmen C. Brewer, Christopher Zalewski +6 more

Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome

Ophthalmic Genetics(2021)10.1080/13816810.2021.1946704

N/A

0.533DataRank · unranked

34 citations

Cristy A. Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena Schiff, Byron L. Lam +16 more

In vitro modeling and rescue of ciliopathy associated with IQCB1/NPHP5 mutations using patient-derived cells

Stem Cell Reports(2022)10.1016/j.stemcr.2022.08.006

N/A

0.510DataRank · unranked

29 citations

Zepeng Qu, Emily Welby, Hiroko Shimada, Suja Hiriyanna, Milton A. English +4 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

0.489DataRank · unranked

25 citations

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

Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

Clinical Genetics(2023)10.1111/cge.14312

N/A

0.477DataRank · unranked

23 citations

Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy Turriff, Keith Pelstring +22 more

Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome

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

N/A

0.477DataRank · 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

0.425DataRank · unranked

16 citations

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

DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1544

N/A

0.416DataRank · unranked

15 citations

Ellen F. Macnamara, Precilla D’Souza, John Yang, Gilbert Vézina, Undiagnosed Diseases Network +5 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

Chedíak-Higashi Syndrome: Hair-to-toe spectrum

Seminars in Pediatric Neurology(2024)10.1016/j.spen.2024.101168

N/A

0.360DataRank · unranked

10 citations

Ariane Soldatos, Camilo Toro, Wadih M. Zein, Joseph Snow, Tanya Lehky +3 more

SLC16A8 is a causal contributor to age-related macular degeneration risk

npj Genomic Medicine(2024)10.1038/s41525-024-00442-8

N/A

0.208DataRank · unranked

3 citations

Bailey Hannon Gussler, Amy Stockwell, Tom Truong, Gyeong Jin Kang, Kristen Browder +19 more

PARK7-Related Early Onset Parkinson Disease in the Setting of Complete Uniparental Isodisomy of Chromosome 1

Neurology Genetics(2021)10.1212/nxg.0000000000000606

N/A

0.208DataRank · unranked

3 citations

Thomas C. Markello, Wadih M. Zein, Rachel Bishop, Catherine Groden, William A. Gahl +2 more

Evolution of focal choroidal excavation in ABCA4-related retinopathy

American Journal of Ophthalmology Case Reports(2022)10.1016/j.ajoc.2022.101740

N/A

0.165DataRank · unranked

2 citations

Carly B. Feldman, Wadih M. Zein, Matthew D. Benson

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

0.104DataRank · unranked

1 citations

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

Variants in CFAP410 cause a range of retinal and skeletal phenotypes

npj Genomic Medicine(2025)10.1038/s41525-025-00489-1

N/A

0DataRank · unranked

0 citations

Amy E. Pohodich, David G. Birch, Kaylie Webb-Jones, Byron L. Lam, Emily H. Jung +44 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

Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome

Clinical Genetics(2020)10.1111/cge.13868

N/A

0DataRank · unranked

37 citations

Rabia Faridi, Kelly King, Christopher Zalewski, Rizwan Yousaf, Julie M. Schultz +9 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

Giant axonal neuropathy: cross-sectional analysis of a large natural history cohort

Brain(2021)10.1093/brain/awab179

N/A

0DataRank · unranked

38 citations

Gina Norato, Dimah Saade, Eduardo Paredes, Victoria Biancavilla, Sandra Donkervoort +14 more

Active Cell Appearance Model Induced Generative Adversarial Networks for Annotation-Efficient Cell Segmentation and Identification on Adaptive Optics Retinal Images

IEEE Transactions on Medical Imaging(2021)10.1109/tmi.2021.3055483

N/A

0DataRank · unranked

22 citations

Christine Shen, Nancy Aguilera, Catherine A. Cukras, Robert B. Hufnagel, Wadih M. Zein +3 more

Auditory and olfactory findings in patients with USH2A‐related retinal degeneration—Findings at baseline from the rate of progression in USH2A‐related retinal degeneration natural history study (RUSH2A)

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62437

N/A

0DataRank · unranked

10 citations

Carmen C. Brewer, Peiyao Cheng, Jacque L. Duncan, Maureen G. Maguire, Isabelle Audo +11 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

A de novo hexokinase 1 (HK1) variant presenting as Boucher–Neuhäuser syndrome

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63045

N/A

0DataRank · unranked

6 citations

Wadih M. Zein, Robert B. Hufnagel, Christine W. Ku, Rena A. Godfrey, Lynne A. Wolfe +4 more

ABCA4c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease

Investigative Ophthalmology & Visual Science(2022)10.1167/iovs.63.4.20

N/A

0DataRank · unranked

7 citations

Manar Salameh, Mubeen Khan, Elise Héon, Ketan Mishra, Rebekkah J. Hitti‐Malin +12 more

Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosis

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2022)10.1002/ajmg.c.31966

N/A

0DataRank · unranked

4 citations

Melissa A. Parisi, Burak Altintas, May Christine V. Malicdan, Thierry Vilboux, Jasmine Knoll +6 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

Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants

Clinical Genetics(2024)10.1111/cge.14614

N/A

0DataRank · unranked

11 citations

Vincent De Man, Isabelle Audo, Irina Balikova, Wadih M. Zein, Vasily Smirnov +20 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

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

Wadih M. Zein

Indexed papers

Top data-sharing exemplar

Papers