Sheng‐Jia Lin

ChemistryBiochemistry, 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 18 papers. Top paper: “Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans”.

Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.29.222828

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0DataRank · unranked

3 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +19 more

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Human Genetics(2021)10.1007/s00439-020-02254-z

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0DataRank · unranked

28 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +21 more

Acrylic boronate: a multifunctional C3 building block for catalytic synthesis of rare organoborons and chemoselective heterobifunctional ligations

Chemical Science(2021)10.1039/d1sc00905b

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0DataRank · unranked

10 citations

Lucia Wang, Abhishek Sharma, Sheng‐Jia Lin

Cnr2 Is Important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors

Frontiers in Molecular Neuroscience(2021)10.3389/fnmol.2021.624265

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0DataRank · unranked

4 citations

Roberto Rodríguez‐Morales, Alexis Santana-Cruz, Juan A. Cantres-Velez, Aranza Torrado-Tapias, Sheng‐Jia Lin +8 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

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29 citations

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

Boron-promoted Deprotonative Conjugate Addition: Development of Geminal diborons as Versatile Soft Pronucleophiles and Acyl An-ion Equivalents

ChemRxiv(2022)10.26434/chemrxiv-2022-kbb2w

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0DataRank · unranked

1 citations

Sheng‐Jia Lin, Emmanuel Santos, Jenna Pralat, Kaylyn Spotton, Abhishek Sharma +1 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

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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

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0DataRank · unranked

19 citations

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

Generation and Application of Homoallylic α,α‐Diboryl Radicals via Diboron‐Promoted Ring‐Opening of Vinyl Cyclopropanes: cis‐Diastereoselective Borylative Cycloaddition**

Chemistry - A European Journal(2023)10.1002/chem.202303175

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0DataRank · unranked

18 citations

Ashvin J. Gangani, Aiswarya Mini, Sheng‐Jia Lin, Jia‐Min Chu, Caitlyn O. Agee +5 more

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

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

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0DataRank · unranked

29 citations

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

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0DataRank · unranked

5 citations

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

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2 citations

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

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0DataRank · unranked

7 citations

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

Biallelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a syndromic neurodevelopmental disorder

medRxiv(2024)10.1101/2024.07.18.24310581

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1 citations

Cailyn P Leo, Chenghong Deng, Kejia Zhang, Sheng‐Jia Lin, Reza Maroofian +75 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

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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

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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

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0DataRank · unranked

3 citations

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

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0DataRank · unranked

2 citations

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