🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Antonie D. Kline

Greater Baltimore Medical Center

ORCID: 0000-0002-7863-2994

Also affiliated with Rambam Health Care Campus

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

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 6 papers. Top paper: “An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome”.

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.014
N/A
0.546DataRank · unranked
37 citations

Vanda McNiven, Cheryl Cytrynbaum, Maryam Jangjoo, Margaret P Adam, Hans T. Björnsson +57 more

Repetitive and Self-injurious Behaviors in Children with Cornelia de Lange Syndrome

Journal of Autism and Developmental Disorders(2020)10.1007/s10803-020-04617-x
N/A
0DataRank · unranked
11 citations

Bennett W. Clark, Colleen Landy‐Schmitt, Elizabeth A. Offermann, Antonie D. Kline, Samuel T. Wilkinson +2 more

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63247
N/A
0DataRank · unranked
41 citations

Justin Blair, Batsal Devkota, Sierra Fortunato, Dinah Clark, Audrey Lawrence +92 more

An expansion of the phenotype in individuals with SYNCRIP-Related Neurodevelopmental Disorder

Rare(2024)10.1016/j.rare.2024.100052
N/A
0DataRank · unranked
4 citations

Joanna L. Feng, Lindsay A. Phillips, Kara Murias, Marcia Ferguson, Kristin Barañano +26 more

Neurobehavioral and developmental profiles: genotype–phenotype correlations in individuals with Cornelia de Lange syndrome

Orphanet Journal of Rare Diseases(2024)10.1186/s13023-024-03104-1
N/A
0DataRank · unranked
3 citations

Julia T. O’Connor, Deirdre Summa, Antonie D. Kline, Rowena Ng

Sleep correlates of behavior functioning in Cornelia de Lange syndrome

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63793
N/A
0DataRank · unranked
1 citations

Marco A. Grados, Julia T. O’Connor, Deirdre Summa, Antonie D. Kline, Rowena Ng