Ayman W. El‐Hattab

Economics, Econometrics and FinanceBiochemistry, 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 10 papers. Top paper: “Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency”.

Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency

Human Molecular Genetics(2022)10.1093/hmg/ddac098

N/A

0.345DataRank · unranked

9 citations

Anna Lena Burgemeister, Vincent Cantagrel, Jeanne Amiel, Karine Siquier-Pernet, Nathalie Boddaert +16 more

Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features

Human Mutation(2020)10.1002/humu.24009

N/A

0DataRank · unranked

19 citations

Cheryl Dickerson, Myra Wick, Najla Al‐Sweel, Amanda Openshaw, Siddharth Srivastava +10 more

Clinician-centric diagnosis of rare genetic diseases: performance of a gene pertinence metric in decision support for clinicians

Orphanet Journal of Rare Diseases(2020)10.1186/s13023-020-01461-1

N/A

0DataRank · unranked

10 citations

Renee D. George, Peter Waltman, Ayman W. El‐Hattab, Kiely N. James, Valentina Stanley +2 more

Biallelic GRM7 variants cause epilepsy, microcephaly, and cerebral atrophy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51003

N/A

0DataRank · unranked

30 citations

Tadahiro Mitani, Sedat Işıkay, Jozef Hertecant, Mohammed Almannai, Kandamurugu Manickam +19 more

Mitochondrial DNA maintenance defects: potential therapeutic strategies

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.07.003

N/A

0DataRank · unranked

20 citations

Ayman W. El‐Hattab, Mahshid S. Azamian, M. Nadir Ali, Fernando Scaglia, Mohammed Almannai

Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease

Brain(2023)10.1093/brain/awad434

N/A

0DataRank · unranked

8 citations

Xinfu Jiao, J. Christopher Hennings, Jan Giesecke, Geeta Palsule, Stefanie Beck‐Wödl +35 more

Constructing and interpreting a large-scale variant effect map for an ultrarare disease gene: Comprehensive prediction of the functional impact of PSAT1 genotypes

PLoS Genetics(2023)10.1371/journal.pgen.1010972

N/A

0DataRank · unranked

5 citations

Gareth A. Cromie, Katherine Owens, Martin S. Timour, Michelle Tang, J. Nathan Kutz +4 more

Predicting the functional effect of compound heterozygous genotypes from large scale variant effect maps

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.11.523651

N/A

0DataRank · unranked

1 citations

Gareth A. Cromie, Katherine Owens, Martin S. Timour, Michelle Tang, J. Nathan Kutz +4 more

Clinical trials in mitochondrial disorders, an update

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.10.002

N/A

0DataRank · unranked

73 citations

Ayman W. El‐Hattab, M. Nadir Ali, Claudia Soler‐Alfonso, Fernando Scaglia, Mohammed Almannai

Biallelic LGI1 and ADAM23 variants cause hippocampal epileptic encephalopathy via the LGI1–ADAM22/23 pathway

Brain(2025)10.1093/brain/awaf202

N/A

0DataRank · unranked

3 citations

Yuri Miyazaki, Daisuke Ishikawa, Hiroki Inahashi, Zuhair N. Al‐Hassnan, Giovanni Zifarelli +20 more