Kevin Huang

Biochemistry, Genetics and Molecular Biology

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 11 papers. Top paper: “ABE-ultramax for high-efficiency biallelic adenine base editing in zebrafish”.

ABE-ultramax for high-efficiency biallelic adenine base editing in zebrafish

Nature Communications(2024)10.1038/s41467-024-49943-1

N/A

0.515DataRank · unranked

30 citations

Fang Ting Liang, Sheng‐Jia Lin, Cassidy Petree, Kevin Huang, Yu Zhang +6 more

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.015

N/A

0.312DataRank · unranked

7 citations

Cailyn P Leo, Chenghong Deng, Sheng‐Jia Lin, Reza Maroofian, Reneé C. Lin +95 more

Uncovering dual molecular diagnoses in families with complex phenotypes through structural and clinical studies of novel COL4A6 variants

QJM(2025)10.1093/qjmed/hcaf246

N/A

0.208DataRank · unranked

3 citations

Abolfazl Rad, Constantin Cretu, Sheng‐Jia Lin, Hafiz Saad Bin Mustafa, Kevin Huang +8 more

Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy

Nature Communications(2024)10.1038/s41467-024-51310-z

N/A

0DataRank · unranked

5 citations

Vincent Francis, Sheng‐Jia Lin, Fares Kharfallah, Vladimir S. Fonov, Maxime Lévesque +80 more

Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function

Human Mutation(2022)10.1002/humu.24435

N/A

0DataRank · unranked

29 citations

Barbara Vona, Hillary M. Porter, Mahmoud Izadi, Kevin Huang, Yves Lacassie +20 more

Naa80 is required for actin N-terminal acetylation and normal hearing in zebrafish

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.17.585386

N/A

0DataRank · unranked

0 citations

Sheng‐Jia Lin, Lars Ole Sti Dahl, Kevin Huang, Cassidy Petree, Gaurav K. Varshney +2 more

Optimizing gRNA selection for high-penetrance F0 CRISPR screening for interrogating disease gene function

Nucleic Acids Research(2025)10.1093/nar/gkaf180

N/A

0DataRank · unranked

11 citations

Kevin Huang, Cassidy Petree, Wei Qin, Pratishtha Varshney, Gaurav K. Varshney +1 more

Rationally Designed TadA‐Derived Cytosine Editors Enable Context‐Independent Zebrafish Genome Editing

Advanced Science(2025)10.1002/advs.202509800

N/A

0DataRank · unranked

3 citations

Sheng‐Jia Lin, Yu Zhang, Kevin Huang, Cassidy Petree, Kevin Boyd +3 more

Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.002

N/A

0DataRank · unranked

2 citations

Sheng‐Jia Lin, Reza Maroofian, Alper Gezdirici, Hamoud Alhebby, Aurélien Trimouille +30 more

Loss of symmetric cell division of apical neural progenitors drives DENND5A -related developmental and epileptic encephalopathy

medRxiv(2022)10.1101/2022.08.23.22278845

N/A

0DataRank · unranked

0 citations

Vincent Francis, Sheng‐Jia Lin, Fares Kharfallah, Vladimir S. Fonov, Maxime Levesque +80 more

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

Brain(2023)10.1093/brain/awad380

N/A

0DataRank · unranked

19 citations

Abolfazl Rad, Sheng‐Jia Lin, Aida M. Bertoli‐Avella, Wouter W. Kallemeijn, Annie Godwin +84 more