Evangeline C. Kurtz‐Nelson

Also affiliated with Indiana University – Purdue University Indianapolis

NeuroscienceBiochemistry, Genetics and Molecular BiologyMathematicsSocial SciencesPsychology

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 17 papers. Top paper: “The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects”.

The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects

Science Advances(2021)10.1126/sciadv.abe2626

N/A

0.581DataRank · unranked

47 citations

Naihua N. Gong, Samuel J. Belfer, Lara V. van Renssen, Evangeline C. Kurtz‐Nelson, Milán Szuperák +16 more

Characterizing the autism spectrum phenotype in DYRK1A‐related syndrome

Autism Research(2023)10.1002/aur.2995

N/A

0.373DataRank · unranked

11 citations

Hannah M. Rea, Aiva C. Petriceks, Caitlin M. Hudac, Tianyun Wang, Rachel K. Earl +4 more

Genetic Ablation of GIGYF1, Associated With Autism, Causes Behavioral and Neurodevelopmental Defects in Zebrafish and Mice

Biological Psychiatry(2023)10.1016/j.biopsych.2023.02.993

N/A

0.345DataRank · unranked

9 citations

Guiyang Huang, Tianyun Wang, Weicheng Duan, Hua Li, Yirong Wang +14 more

Unpacking The Autism Spectrum Disorder Profile of Children With De Novo Disruptive GRIN2B Variants: A Quantitative and Qualitative Analysis

Research Square (Research Square)(2020)10.21203/rs.3.rs-76658/v1

N/A

0DataRank · unranked

0 citations

Evangeline C. Kurtz‐Nelson, Tara M. Rutter, Jessica L. Peterson, Kendra Hoekzema, Jennifer S. Beighley +7 more

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

Nature Genetics(2021)10.1038/s41588-021-00886-z

N/A

0DataRank · unranked

108 citations

Blake A. Creighton, Keith A. Breau, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +70 more

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.015

N/A

0DataRank · unranked

93 citations

Kaifang Pang, Andrea Ciolfi, Michael A. Levy, Andrés Hernández, Lucia Pedace +95 more

Family Empowerment: Predicting Service Utilization for Children with Autism Spectrum Disorder

Journal of Autism and Developmental Disorders(2021)10.1007/s10803-021-05329-6

N/A

0DataRank · unranked

5 citations

Evangeline C. Kurtz‐Nelson, Hannah Barton, Jonathan Safer‐Lichtenstein, Laura Lee McIntyre, Patricia K. Zemantic

GIGYF1 disruption associates with autism and impaired IGF-1R signaling

Journal of Clinical Investigation(2022)10.1172/jci159806

N/A

0DataRank · unranked

32 citations

Bin Yu, Senwei Tan, Jieqiong Tan, Xiangbin Jia, Qiumeng Zhang +29 more

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Genetics in Medicine(2022)10.1016/j.gim.2022.04.010

N/A

0DataRank · unranked

21 citations

Marieke Joosten, Caroline Alby, Tania Attié‐Bitach, Kelly L. Gilmore, Christèle Dubourg +50 more

Rhythmic attentional sampling in autism

Autism Research(2023)10.1002/aur.3021

N/A

0DataRank · unranked

2 citations

Tamar Kolodny, Kristin Woodard, Aydin Tasevac, Wesley R. Ganz, Hannah M. Rea +4 more

Shared and divergent mental health characteristics of ADNP-, CHD8- and DYRK1A-related neurodevelopmental conditions

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09532-1

N/A

0DataRank · unranked

8 citations

Hannah M. Rea, Elizabeth Jones, Hannah R. Benavidez, Conor Miles, Alana Whiting +7 more

ARID1B-related disorder in 87 adults: Natural history and self-sustainability

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101873

N/A

0DataRank · unranked

6 citations

M. Gösgens, Alexander J.M. Dingemans, P. Striano, Antonella Riva, C. Mignot +81 more

Visual and auditory attention in individuals with DYRK1A and SCN2A disruptive variants

Autism Research(2024)10.1002/aur.3202

N/A

0DataRank · unranked

5 citations

Kelsey Dommer, Monique Mahony, Trent D. DesChamps, Brianna E. Cairney, Rachel K. Earl +8 more

Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.07.003

N/A

0DataRank · unranked

54 citations

Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa +24 more

Characterizing executive functioning and associated behaviors in individuals with dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) syndrome

Frontiers in Neuroscience(2025)10.3389/fnins.2024.1485499

N/A

0DataRank · unranked

0 citations

Sara Jane Webb, Evangeline C. Kurtz‐Nelson, Caitlin M. Hudac, Raphael Bernier, Conor Miles +8 more

Episignatures stratifying ADNP syndrome show modest correlation with phenotype

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.014902

N/A

0DataRank · unranked

7 citations

Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa +23 more

Pathogenic SPTBN1 variants cause a novel autosomal dominant neurodevelopmental syndrome

medRxiv(2020)10.1101/2020.08.31.20184481

N/A

0DataRank · unranked

3 citations

Keith A. Breau, Blake A. Creighton, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +63 more