Erica Schindewolf

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 8 papers. Top paper: “Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition”.

Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition

JCI Insight(2023)10.1172/jci.insight.155888

N/A

0.550DataRank · unranked

38 citations

Michael March, Christoph Seiler, Leticia S. Matsuoka, S Kim, Charlly Kao +28 more

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age

American Journal of Obstetrics and Gynecology(2023)10.1016/j.ajog.2023.09.005

N/A

0.485DataRank · unranked

15 citations

Stephanie Galloway, T. Blaine Crowley, Julie S. Moldenhauer, Ann Swillen, Jeroen Breckpot +57 more

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624

N/A

0.464DataRank · unranked

21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation

Prenatal Diagnosis(2024)10.1002/pd.6566

N/A

0DataRank · unranked

7 citations

Anne S. Bassett, Erik Boot, Bruno Marino, Julie S. Moldenhauer, Sólveig Óskarsdóttir +6 more

Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61531

N/A

0DataRank · unranked

13 citations

Stanley M. Kanai, Bryan L. Krock, Erica Schindewolf, Jennifer Oliver‐Krasinski, Nahla Khalek +6 more

An Unusual Cause of Hexokinase 1 Deficiency—Case Report

eJHaem(2025)10.1002/jha2.70123

N/A

0DataRank · unranked

0 citations

Kelly Maurer, Tanaya Jadhav, Tejas Jammihal, Zhe Zhang, Helge Hartung +11 more

The importance of patient‐specific resources for families dealing with prenatal rare diseases

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63450

N/A

0DataRank · unranked

2 citations

Jennifer Ortiz Cutshall, Lex van der Heijden, Erica Schindewolf, Sarah E. Sheppard, Dhyanam P. Shukla

Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter study

American Journal of Obstetrics and Gynecology(2024)10.1016/j.ajog.2024.06.025

N/A

0DataRank · unranked

9 citations

Mohamad Ali Maktabi, Alexandra Tinfow, Jessica L. Giordano, Thomas M. Heisler, Qi Yan +22 more