Angela E. Lin

Also affiliated with National Center on Birth Defects and Developmental Disabilities

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 19 papers. Top paper: “Characteristics of Adults With Congenital Heart Defects in the United States”.

Characteristics of Adults With Congenital Heart Defects in the United States

Journal of the American College of Cardiology(2020)10.1016/j.jacc.2020.05.025

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0DataRank · unranked

63 citations

Julie E. Dunn, Ami B. Bhatt, Wendy Book, Jill Glidewell, Carol Hogue +9 more

Damaging de novo missense variants inEEF1A2lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy

Human Mutation(2020)10.1002/humu.24015

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0DataRank · unranked

40 citations

Katherine L. Helbig, Candace T. Myers, Marcello Scala, Robert Huether, Sara A. Lewis +40 more

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

UNC Libraries(2020)10.17615/nh7z-zg10

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1 citations

Kathryn F. Peters, Lewis B. Holmes, David J. Aughton, Laura Mazzanti, Kathleen A. Leppig +27 more

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

UNC Libraries(2020)10.17615/tdb3-bx52

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0DataRank · unranked

0 citations

Hemant Bengani, Joseph A. Marsh, Angela M. Kaindl, Koh-ichiro Yoshiura, Katharina Steindl +73 more

Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62194

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12 citations

Nisha Patel, John M. Graham, Michael J. Bamshad, Deborah A. Nickerson, Janson J. White +10 more

Multiplex Base-Editing Enables Combinatorial Epigenetic Regulation for Genome Mining of Fungal Natural Products

Journal of the American Chemical Society(2022)10.1021/jacs.2c10211

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0DataRank · unranked

46 citations

Chunxiao Sun, Zhiwen Liu, Alan Cabrera, Mario Escobar, Shunyu Huang +9 more

The human Y and inactive X chromosomes similarly modulate autosomal gene expression

Cell Genomics(2023)10.1016/j.xgen.2023.100462

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0DataRank · unranked

51 citations

Helen Skaletsky, Alexander K. Godfrey, Neha V. Bokil, Levi S. Teitz, Isani Singh +22 more

Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000–2017: A report from the National Birth Defects Prevention Network

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63181

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27 citations

Angela E. Lin, Sonja A. Rasmussen, Russell S. Kirby, Eirini Nestoridi, Rebecca F. Liberman +15 more

Safety, tolerability, and effectiveness of anticoagulation and antiplatelet therapy in hereditary hemorrhagic telangiectasia

Journal of Thrombosis and Haemostasis(2023)10.1016/j.jtha.2022.09.003

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0DataRank · unranked

13 citations

Ellen Zhang, Josanna Rodriguez‐Lopez, Alison S. Witkin, Alexandra K. Wong, Jay Luther +6 more

Multifocal heterotopic ossification in a man with germline variants of LIM Mineralization Protein‐1 (LMP‐1)

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63304

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1 citations

Eileen M. Shore, Meiqi Xu, Clemens Bergwitz, Santiago A. Lozano‐Calderón, Angela E. Lin +3 more

The human Y and inactive X chromosomes similarly modulate autosomal gene expression

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.05.543763

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16 citations

Helen Skaletsky, Alexander K. Godfrey, Neha V. Bokil, Levi S. Teitz, Isani Singh +22 more

Correspondence on “Points to consider in the practice of postmortem genetic testing: A statement of the American College of Medical Genetics and Genomics (ACMG)” by Deignan, et al

Genetics in Medicine(2023)10.1016/j.gim.2023.100904

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0DataRank · unranked

0 citations

Kathryn J. Gray, Siddharth K. Prakash, Monica H. Wojcik, Angela E. Lin, Fowzan S. Alkuraya

Clinical practice guidelines for the care of girls and women with Turner syndrome

European Journal of Endocrinology(2024)10.1093/ejendo/lvae050

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0DataRank · unranked

193 citations

N.H. Andersen, Sophie Christin‐Maître, Shanlee Davis, Anthonie L. Duijnhouwer, Aneta Gawlik +71 more

Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types

Cell Genomics(2024)10.1016/j.xgen.2024.100628

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0DataRank · unranked

17 citations

Adrianna K. San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky +10 more

Gain-of-function variants in SMAD4 compromise respiratory epithelial function

Journal of Allergy and Clinical Immunology(2024)10.1016/j.jaci.2024.08.024

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0DataRank · unranked

9 citations

Eleanor R. Scimone, Joseph Lawton, Rashmi Richa, Lael M. Yonker, Y. Peter Di +6 more

Maternal Exposure to Tap Water Disinfection By‐Products and Risk of Selected Congenital Heart Defects

Birth Defects Research(2024)10.1002/bdr2.2391

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0DataRank · unranked

5 citations

Thomas J. Luben, Ibrahim Zaganjor, Anthony Rhoads, Paul A. Romitti, Kristin M. Conway +11 more

Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101851

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4 citations

Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Rotem Haklai +72 more

Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.18.585578

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0DataRank · unranked

1 citations

Adrianna K. San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky +10 more

Artificial intelligence-driven genotype–epigenotype–phenotype approaches to resolve challenges in syndrome diagnostics

EBioMedicine(2025)10.1016/j.ebiom.2025.105677

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0DataRank · unranked

6 citations

Hannah Klinkhammer, Sanaa Choufani, Nikola Reko, Angela K Christman, Elise Pisan +36 more