Ann M. Neumeyer

Also affiliated with Center for Autism and Related Disorders

NeuroscienceMedicinePsychologyBiochemistry, 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: “NNZ-2591 in Children and Adolescents With Phelan-McDermid Syndrome”.

NNZ-2591 in Children and Adolescents With Phelan-McDermid Syndrome

Neurology Genetics(2025)10.1212/nxg.0000000000200338

N/A

0.104DataRank · unranked

1 citations

Siddharth Srivastava, J. Lloyd Holder, Mark A. Milad, Liza Squires, Nancy E. Jones +3 more

A novel fast-channel myasthenia caused by mutation in β subunit of AChR reveals subunit-specific contribution of the intracellular M1-M2 linker to channel gating

Experimental Neurology(2020)10.1016/j.expneurol.2020.113375

N/A

0DataRank · unranked

9 citations

Li Di, Shelley Shen, Yuying Zhao, Ann M. Neumeyer, Duygu Selcen +3 more

Updated consensus guidelines on the management of Phelan–McDermid syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63312

N/A

0DataRank · unranked

49 citations

Mustafa Sahin, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Latha Soorya, Audrey Thurm +40 more

Optimizing Care for Autistic Patients in Health Care Settings: A Scoping Review and Call to Action

Academic Pediatrics(2023)10.1016/j.acap.2023.11.006

N/A

0DataRank · unranked

14 citations

Laura Weissman, Eron Friedlaender, Ann M. Neumeyer, Alexander Friedman, Sarah Spence +5 more

The spectrum of neurological presentation in individuals affected by TBL1XR1 gene defects

Orphanet Journal of Rare Diseases(2024)10.1186/s13023-024-03083-3

N/A

0DataRank · unranked

5 citations

Francine Molay, Sarah Hargadon, Cláudia Brito Pires, Natalie Grant, Lizbeth De La Rosa Abreu +10 more

Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.018

N/A

0DataRank · unranked

6 citations

Laura Harrold, Daniel G. Calame, Claire Salter, Takashi Kikuma, Kevin P. Guay +49 more