Chad Haldeman‐Englert

Biochemistry, Genetics and Molecular BiologyMedicine

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: “Microduplications of 16p11.2 are associated with schizophrenia”.

Microduplications of 16p11.2 are associated with schizophrenia

Nature Genetics(2009)10.1038/ng.474

N/A

0.990DataRank · unranked

733 citations

Kenneth S. Kendler, Manfred Kayser, Anjene M Addington, Jon McClellan, Milica Pejović-Milovančević +66 more

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Genetics in Medicine(2021)10.1038/s41436-021-01152-7

N/A

0.515DataRank · unranked

30 citations

Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra London +95 more

Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.009

N/A

0.396DataRank · unranked

13 citations

Ashish R. Deshwar, Yan Huang, Scott Barish, Xi Zhang, Sanaa Choufani +30 more

Question prompt lists and caregiver question asking in pediatric specialty appointments: A randomized controlled trial

Patient Education and Counseling(2023)10.1016/j.pec.2022.107620

N/A

0.312DataRank · unranked

7 citations

Haoyang Yan, R. Jean Cadigan, Courtney Canter, Lizzy Bain, Jeannette T. Bensen +15 more

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder,apraxia, and insensitivity to pain

medRxiv(2020)10.1101/2020.09.10.20190314

N/A

0.104DataRank · unranked

1 citations

Georgi Stoyanov, Florian Erger, Jill A. Rosenfeld, Erin Torti, Chad Haldeman‐Englert +18 more

From Uncertain to Actionable: Significant Reduction in Variants of Uncertain Significance in Hereditary Germline Testing via Multi-Institutional Real-World Evidence

medRxiv(2025)10.1101/2025.08.12.25333547

N/A

0DataRank · unranked

0 citations

Matthew J. Ferber, Sophie I. Candille, Ildiko Thibodeau, Daniela Iacoboni, Amy C. Sturm +15 more

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64289

N/A

0DataRank · unranked

0 citations

Chad Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana S. Brightman +10 more

A dyadic approach to the delineation of diagnostic entities in clinical genomics

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2020.11.013

N/A

0DataRank · unranked

116 citations

Margaret P Adam, Fowzan S. Alkuraya, Anne Amemiya, Michael J. Bamshad, Anita E. Beck +42 more

Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genes

Scientific Reports(2021)10.1038/s41598-021-90798-z

N/A

0DataRank · unranked

12 citations

Steven D. Klein, Stephen R. Williams, Jeffrey W. Innis, Frank J. Probst, Chad Haldeman‐Englert +6 more

Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome

PLoS Genetics(2022)10.1371/journal.pgen.1010504

N/A

0DataRank · unranked

14 citations

Renan Paulo Martin, Elizabeth Wohler, Elizabeth Partan, Elizabeth Walek, Shaima Salman +13 more

Question prompt lists and caregiver question asking in pediatric specialty appointments: A randomized controlled trial

UNC Libraries(2024)10.17615/tpm5-8x49

N/A

0DataRank · unranked

0 citations

Michael E. Mahla, Suzanne C. O’Neill, Feng Lin, Geoffrey L. Smith, B. F. Leach +15 more