Anne M. Comi

Medicine

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 11 papers. Top paper: “The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder”.

The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder

Human Mutation(2021)10.1002/humu.24308

N/A

0.921DataRank · unranked

20 citations

Amanda M. Levy, Jaya Punetha, Hua Gao, Nicholas Ah Mew, Kwame Anyane Yeboa +54 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003

N/A

0.564DataRank · unranked

42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100345

N/A

0.292DataRank · unranked

6 citations

Raymond J. Louie, Olivia Larner, Robert G. Best, Kevin Chen, Josephine Morris +27 more

Biomarker development in Sturge-Weber syndrome

Journal of Neurodevelopmental Disorders(2025)10.1186/s11689-025-09640-6

N/A

0.241DataRank · unranked

4 citations

Katharine E. Joslyn, Kieran D. McKenney, Anne M. Comi, Siddharth Gupta

Retrospective analysis of presymptomatic treatment in Sturge–Weber syndrome

Annals of the Child Neurology Society(2024)10.1002/cns3.20058

N/A

0DataRank · unranked

16 citations

Isabelle Iannotti, Eric H. Kossoff, T. Andrew Zabel, Bernard A. Cohen, Yangming Ou +3 more

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.12.004

N/A

0DataRank · unranked

1 citations

Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa S. Rajan, Senta Schönnagel +53 more

Sirolimus Treatment in Sturge-Weber Syndrome

Pediatric Neurology(2020)10.1016/j.pediatrneurol.2020.10.013

N/A

0DataRank · unranked

59 citations

Alyssa M. Day, Joshua B. Ewen, Jack H. Adamek, Anna W. Byars, Bernard A. Cohen +12 more

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

medRxiv(2025)10.1101/2025.03.31.25324695

N/A

0DataRank · unranked

2 citations

Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa Rajan, Senta Schönnagel +54 more

Identification of a Mosaic Activating Mutation in GNA11 in Atypical Sturge-Weber Syndrome

Journal of Investigative Dermatology(2020)10.1016/j.jid.2020.03.978

N/A

0DataRank · unranked

50 citations

Laurence P. Frelin, Meghan McCann, Carlos A. Pardo, Bernard A. Cohen, Anne M. Comi +2 more

Quantitative EEG improves prediction of Sturge-Weber syndrome in infants with port-wine birthmark

Clinical Neurophysiology(2021)10.1016/j.clinph.2021.06.030

N/A

0DataRank · unranked

15 citations

Bo‐Hao Tang, Lindsay Smegal, Jack H. Adamek, Danielle McAuliffe, Balaji M. Lakshmanan +9 more

Study protocol: retrospectively mining multisite clinical data to presymptomatically predict seizure onset for individual patients with Sturge-Weber

BMJ Open(2022)10.1136/bmjopen-2021-053103

N/A

0DataRank · unranked

10 citations

Anna Pinto, Doris Lin, Anne M. Comi, Yangming Ou, Pooja Vedmurthy