Rebecca Hernan

Also affiliated with Harvard University, Boston Children's Museum

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 14 papers. Top paper: “NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism”.

NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.10.002

N/A

0DataRank · unranked

42 citations

Qiumeng Zhang, Rujia Dai, Bin Yu, Kendra Hoekzema, Jieqiong Tan +53 more

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Genetics in Medicine(2020)10.1038/s41436-020-0908-0

N/A

0DataRank · unranked

37 citations

Julia Wynn, Lan Yu, Rebecca Hernan, Xueya Zhou, Vincent Duron +21 more

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.011

N/A

0DataRank · unranked

50 citations

Le Xu, Lan Yu, Julia Wynn, Rebecca Hernan, Xueya Zhou +33 more

A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion

New England Journal of Medicine(2021)10.1056/nejmoa2033911

N/A

0DataRank · unranked

46 citations

Emmanuelle Szenker‐Ravi, Changuk Chung, Zhen Li, Lu Wang, Muznah Khatoo +25 more

Missense variants affecting the actin-binding domains of PLS3 cause X-linked congenital diaphragmatic hernia and body wall defects

medRxiv(2021)10.1101/2021.07.07.21259278

N/A

0DataRank · unranked

2 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Matthew J. Dysart, Hannah T. M. Contreras +33 more

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 and ALYREF as new candidate risk genes

medRxiv(2021)10.1101/2021.06.01.21257928

N/A

0DataRank · unranked

0 citations

Le Xu, Lan Yu, Julia Wynn, Rebecca Hernan, Xueya Zhou +33 more

Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.01.020

N/A

0DataRank · unranked

39 citations

Rebecca Hernan, Paul C. Marcogliese, Yan Huang, Tracy S. Gertler, Meltem Akçaboy +13 more

Extracorporeal Membrane Oxygenation (ECMO) and its complications in newborns with congenital diaphragmatic hernia

Journal of Pediatric Surgery(2022)10.1016/j.jpedsurg.2021.12.028

N/A

0DataRank · unranked

13 citations

Rafael Klein-Cloud, Claire Gerall, Weijia Fan, Jessica Price, Rebecca Hernan +9 more

Congenital Heart Disease with Congenital Diaphragmatic Hernia: Surgical Decision Making and Outcomes

The Journal of Pediatrics(2023)10.1016/j.jpeds.2023.113530

N/A

0DataRank · unranked

13 citations

Rebecca Hernan, Christopher Mardy, Eunice Hahn, Wendy K. Chung, Emile Bacha +4 more

PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.002

N/A

0DataRank · unranked

8 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Eric L. Bogenschutz, Matthew J. Dysart +34 more

Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.08.024

N/A

0DataRank · unranked

14 citations

Carrie L. Welch, Rebecca Hernan, Julia Wynn, Usha Krishnan, Jill M. Zalieckas +46 more

Rescuing lung development through embryonic inhibition of histone acetylation

Science Translational Medicine(2024)10.1126/scitranslmed.adc8930

N/A

0DataRank · unranked

12 citations

Zhuowei Li, Nicole Talaba, William Genthe, Maria B. Brix, Betty Pham +16 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369

N/A

0DataRank · unranked

4 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 more

LONP1 Variants Are Associated With Clinically Diverse Phenotypes

Clinical Genetics(2025)10.1111/cge.70057

N/A

0DataRank · unranked

1 citations

Lu Qiao, Rebecca Hernan, David A. Sweetser, Jessica L. Waxler, Daryl A. Scott +34 more