K. Nicole Weaver

Cincinnati Children's Hospital Medical Center

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

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 10 papers. Top paper: “POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies”.

POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.014

N/A

0.457DataRank · unranked

20 citations

Kristin E.N. Watt, Satoru Ide, Kristina Baltrunaite, Chad Brunswick, Katherine Inskeep +40 more

Genetic and phenotypic heterogeneity in KIAA0753‐related ciliopathies

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62497

N/A

0.312DataRank · unranked

7 citations

Yuri A. Zárate, Danielle Monteil, Jurgen Spranger, Dan Doherty, Rolf W. Stottmann +2 more

Sequencing validates deep learning models for EHR-based detection of Noonan syndrome in pediatric patients

npj Genomic Medicine(2025)10.1038/s41525-025-00512-5

N/A

0.241DataRank · unranked

4 citations

Amy Shikany, Ammar Husami, Xinjian Wang, Eneida Mendonca, K. Nicole Weaver +2 more

Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63397

N/A

0DataRank · unranked

4 citations

April Vanderwal, Sarah E. Chadwell, A.I. Sánchez, Robert J. Hopkin, Robert B. Hufnagel +3 more

MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency Syndrome

American Journal of Neuroradiology(2020)10.3174/ajnr.a6746

N/A

0DataRank · unranked

25 citations

K. Nicole Weaver, Khalid Alhasan, Evren Gümüş, Bonnie Sullivan, Martin Zenker +3 more

Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome

Genetics in Medicine(2024)10.1016/j.gim.2024.101222

N/A

0DataRank · unranked

8 citations

Michael March, Christopher J. Cardinale, Yichuan Liu, Mark R. Battig, Lívia Sertori Finoti +15 more

Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2024)10.1002/ajmg.c.32095

N/A

0DataRank · unranked

3 citations

Andrea Patete, Lindsey Aschbacher‐Smith, Dima Qu’d, Geraldine Kelly‐Mancuso, Carolyn R. Raski +15 more

A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

Nature Communications(2024)10.1038/s41467-023-44506-2

N/A

0DataRank · unranked

16 citations

Eva D’haene, Machteld Baetens, Tara N. Yankee, Emma Wentworth Winchester, Nicole Glidden +13 more

POLRMT mutations impair mitochondrial transcription causing neurological disease

Nature Communications(2021)10.1038/s41467-021-21279-0

N/A

0DataRank · unranked

60 citations

Bradley Peter, Zsolt Szilágyi, Héctor Díaz-Maldonado, Meenakshi Singh, Ewen W. Sommerville +34 more

Stx4 is required to regulate cardiomyocyte Ca2+ handling during vertebrate cardiac development

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100115

N/A

0DataRank · unranked

5 citations

Padmapriyadarshini Ravisankar, Manu Beerens, Lejla Mulahasanovic, Kelly Smallwood, Marion Bermúdez Sasso +9 more