Abdul Nasır

Also affiliated with Second Affiliated Hospital of Zhengzhou University

Environmental ScienceMedicineNeuroscienceVeterinary

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: “Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment”.

Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment

Genes(2020)10.3390/genes11111249

N/A

0DataRank · unranked

20 citations

Isabelle Schrauwen, Kevin Esoh, Thashi Bharadwaj, Liz M. Nouel‐Saied, Anushree Acharya +6 more

A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family

Experimental Biology and Medicine(2021)10.1177/1535370221999746

N/A

0DataRank · unranked

14 citations

Isabelle Schrauwen, Kevin Esoh, Thashi Bharadwaj, Liz M. Nouel‐Saied, Anushree Acharya +4 more

ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment

European Journal of Human Genetics(2021)10.1038/s41431-021-00913-x

N/A

0DataRank · unranked

15 citations

Isabelle Schrauwen, Sakina Rehman, Khurram Liaqat, Anushree Acharya, Arnaud P. J. Giese +19 more

A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

Genes(2021)10.3390/genes12111765

N/A

0DataRank · unranked

9 citations

Isabelle Schrauwen, Leonardo Alves de Souza Rios, Shaheen Mowla, Cedrik Tekendo‐Ngongang, Kalinka Popel +11 more

Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13

Journal of Human Genetics(2021)10.1038/s10038-021-00922-0

N/A

0DataRank · unranked

7 citations

Syed Irfan Raza, Muhammad Zeeshan Anwar, Thashi Bharadwaj, Khurram Liaqat, Muhammad Akram Shahzad Khokhar +9 more

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

Communications Biology(2022)10.1038/s42003-022-03326-8

N/A

0DataRank · unranked

21 citations

Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Edmond Wonkam‐Tingang, Kevin Esoh +17 more