Jonathan H. Sheehan

MedicineBiochemistry, 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 13 papers. Top paper: “Specificity and affinity of the N-terminal residues in staphylocoagulase in binding to prothrombin”.

Specificity and affinity of the N-terminal residues in staphylocoagulase in binding to prothrombin

Journal of Biological Chemistry(2020)10.1074/jbc.ra120.012588

N/A

0.370DataRank · unranked

5 citations

Heather K. Kroh, Mary E. Aschenbrenner, Breanne Gibson, Peter Panizzi, Jonathan H. Sheehan +4 more

Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene (ALPL)

Journal of the Endocrine Society(2020)10.1210/jendso/bvaa084

N/A

0DataRank · unranked

9 citations

Jonathan H. Sheehan, John H. Newman, Jens Meiler, John A. Capra, Andrea H. Ramirez +3 more

Co-occurring gain-of-function mutations in HER2 and HER3 modulate HER2/HER3 activation, oncogenesis, and HER2 inhibitor sensitivity

Cancer Cell(2021)10.1016/j.ccell.2021.06.001

N/A

0DataRank · unranked

103 citations

Benjamin P. Brown, Jens Meiler, Arnaldo Marín, Harikrishna Sekar Jayanthan, Dan Ye +13 more

Modeling Immunity with Rosetta: Methods for Antibody and Antigen Design

Biochemistry(2021)10.1021/acs.biochem.0c00912

N/A

0DataRank · unranked

62 citations

Samuel Schmitz, Jared Adolf‐Bryfogle, Alexander M. Sevy, Jessica A. Finn, Marion F. Sauer +20 more

Familial Autonomic Ganglionopathy Caused by Rare CHRNA3 Genetic Variants

Neurology(2021)10.1212/wnl.0000000000012143

N/A

0DataRank · unranked

15 citations

Karen M. Joos, John A. Phillips, Joy D. Cogan, John H. Newman, Rizwan Hamid +10 more

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100131

N/A

0DataRank · unranked

11 citations

Thomas Cassini, Ningning Hu, Tao Yang, Bian Li, Wangzhen Shen +13 more

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

medRxiv(2022)10.1101/2022.02.01.21268115

N/A

0DataRank · unranked

1 citations

Thomas Cassini, Ningning Hu, Tao Yang, Bian Li, Wangzhen Shen +14 more

Molecular mechanisms of catalytic inhibition for active site mutations in glucose-6-phosphatase catalytic subunit 1 linked to glycogen storage disease

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.03.13.532485

N/A

0DataRank · unranked

1 citations

Richard A. Stein, Jonathan H. Sheehan, Emily M. Hawes, Richard M. O’Brien, Emad Tajkhorshid +2 more

Integrative analysis of pathogenic variants in glucose-6-phosphatase based on an AlphaFold2 model

PNAS Nexus(2024)10.1093/pnasnexus/pgae036

N/A

0DataRank · unranked

7 citations

Richard A. Stein, Jonathan H. Sheehan, Emily M. Hawes, Richard M. O’Brien, Emad Tajkhorshid +2 more

Recurrent p.H119Y variant in MAP2K1 expands the phenotypic spectrum of MAP2K1‐related RASopathy

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63854

N/A

0DataRank · unranked

0 citations

Daniel Wegner, Jennifer Wambach, Kathleen Sisco, Stephen Stone, Jonathan H. Sheehan +6 more

Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal recessive condition

Molecular Genetics and Metabolism Reports(2024)10.1016/j.ymgmr.2024.101145

N/A

0DataRank · unranked

0 citations

Yutaka Furuta, Devin Oglesbee, Enikö K. Pivnick, David C. Rinker, Jonathan H. Sheehan +9 more

Integrating structural and evolutionary data to interpret variation and pathogenicity in adapter protein complex 4

Protein Science(2020)10.1002/pro.3870

N/A

0DataRank · unranked

14 citations

Abin Abraham, Carli D. Needle, Christopher W. Moth, Jonathan H. Sheehan, John A. Capra +2 more

Phenotypic Variability and Paternal Inheritance of a CHD8 Variant Causing Intellectual Developmental Disorder With Autism and Macrocephaly Confirmed by Epigenetic and Structural Analyses

Molecular Genetics & Genomic Medicine(2025)10.1002/mgg3.70165

N/A

0DataRank · unranked

0 citations

Kimberly Ezell, Rizwan Hamid, Joy D. Cogan, Thomas Cassini, Lynette Rives +23 more