Shekeeb S. Mohammad

PsychologyMedicine

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

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 8 papers. Top paper: “Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition”.

Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition

Molecular Psychiatry(2023)10.1038/s41380-022-01852-9

N/A

0.538DataRank · unranked

35 citations

Michael Pusch, Alessandra Picollo, Caitlin Forwood, Matthew H. Nguyen, Vanessa Suckow +94 more

A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy

Molecular Case Studies(2021)10.1101/mcs.a005827

N/A

0.520DataRank · unranked

31 citations

Melissa Walker, Frances A. High, Cynthia A. Cooper, Cassandra A. Rogers, Christine J. Callahan +14 more

Single-Cell RNA Sequencing in Incontinentia Pigmenti With Neonatal Encephalopathy Reveals Broad Immune Activation Moderated by Steroids

Neurology Neuroimmunology & Neuroinflammation(2025)10.1212/nxi.0000000000200358

N/A

0.269DataRank · unranked

5 citations

Velda Han, Brian Gloss, Brooke Keating, Hiroya Nishida, Xianzhong Lau +4 more

Psychiatric comorbidity is common in dystonia and other movement disorders

Archives of Disease in Childhood(2020)10.1136/archdischild-2020-319541

N/A

0DataRank · unranked

5 citations

Isobel Heyman, Benjamin Baig, Anna Coughtrey, Andrew McWilliams, David Dossetor +13 more

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.019

N/A

0DataRank · unranked

47 citations

Heidi Cope, Zelha Nil, Thomas A. Ravenscroft, Wu‐Lin Charng, Shenzhao Lu +42 more

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

Genetics in Medicine(2020)10.1038/s41436-020-00988-9

N/A

0DataRank · unranked

56 citations

Trine Bjørg Hammer, Elena Gardella, Danique R.M. Vlaskamp, Birgitte Bertelsen, Simone Mandelstam +80 more

The Spectrum of Neurologic Phenotypes Associated With NUS1 Pathogenic Variants: A Comprehensive Case Series

Annals of Neurology(2025)10.1002/ana.27272

N/A

0DataRank · unranked

8 citations

María Novelli, Robert Coukos, Neha Prakash, Walaa A. Kamel, Marta Amengual‐Gual +75 more

Gain-of-function GABRB3 variants identified in vigabatrin-hypersensitive epileptic encephalopathies

Brain Communications(2020)10.1093/braincomms/fcaa162

N/A

0DataRank · unranked

35 citations

Vivian W. Y. Liao, Kavitha Kothur, Dinesh C. Indurthi, Bruce Bennetts, Christopher Troedson +16 more