Wasim Ahmad

Also affiliated with University of Engineering and Technology Taxila, Petronas (Malaysia), Ernst Abbe University of Applied Sciences Jena, Amplyx Pharmaceuticals (United States), Friedrich Schiller University Jena

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

1in 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 1 indexed paper 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 11 papers. Top paper: “Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia”.

Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia

The Journal of Gene Medicine(2024)10.1002/jgm.3601

N/A

0.292DataRank · unranked

6 citations

Asmat Ullah, Nighat Haider, Sufyan Suleman, Fati Ullah Khan, Abid Ali Shah +4 more

Syntaxin 4 is essential for hearing in human and zebrafish

Human Molecular Genetics(2022)10.1093/hmg/ddac257

N/A

0.208DataRank · unranked

3 citations

Amama Ghaffar, Thashi Bharadwaj, Khadim Shah, Sakina Rehman, Anushree Acharya +9 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

Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

Journal of Human Genetics(2021)10.1038/s10038-021-00954-6

N/A

0DataRank · unranked

14 citations

Isabelle Schrauwen, Elvis Twumasi Aboagye, Thashi Bharadwaj, Kevin Esoh, Sulman Basit +10 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

Issue Information

Human Mutation(2018)10.1002/humu.23568

N/A

0DataRank · unranked

0 citations

R. Donald Harvey, Tracy Dudding‐Byth, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel +135 more

LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertility

eLife(2023)10.7554/elife.90095

N/A

0DataRank · unranked

9 citations

Pengxin Chai, Shoaib Nawaz, Jungmin Choi, Francesc López‐Giráldez, Shabir Hussain +7 more

LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertility

eLife(2023)10.7554/elife.90095.3

N/A

0DataRank · unranked

8 citations

Pengxin Chai, Shoaib Nawaz, Jungmin Choi, Francesc López‐Giráldez, Shabir Hussain +7 more

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

BMC Medical Genomics(2024)10.1186/s12920-024-02060-w

N/A

0DataRank · unranked

1 citations

Anushree Acharya, Fati Ullah Khan, Saadullah Khan, Irfan Ullah, Isabelle Schrauwen +3 more

Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

Nature Genetics(2025)10.1038/s41588-025-02332-w

N/A

0DataRank · unranked

1 citations

Inna A. Belyantseva, Arnaud P. J. Giese, Kwanghyuk Lee, Artur A. Indzhykulian, Sri Pratima Nandamuri +26 more

Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.662903

N/A

0DataRank · unranked

78 citations

Shoaib Nawaz, Jungmin Choi, Huafeng Wang, Shabir Hussain, Mehboob Nawaz +12 more