Sheikh Riazuddin

Also affiliated with Allama Iqbal Medical College, University of Health Sciences Lahore

NeuroscienceMedicineBiochemistry, 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

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 15 papers. Top paper: “Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan”.

Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

BMC Medical Genetics(2004)10.1186/1471-2350-5-24

N/A

0.550DataRank · unranked

38 citations

Xiaoyan Cindy Li, Shontell D Powell, Saima Riazuddin, Terry-Lynn Young, Khushnooda Ramzan +12 more

Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features

European Journal of Human Genetics(2020)10.1038/s41431-020-0669-x

N/A

0.546DataRank · unranked

37 citations

Geok Lin Chua, Cheen Fei Chin, Hessa S. Alsaif, Artem Borovikov, Saima Riazuddin +25 more

Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

Clinical Genetics(2023)10.1111/cge.14312

N/A

0.477DataRank · unranked

23 citations

Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy Turriff, Keith Pelstring +22 more

Mutations in ZBTB20 in individuals with persistent stuttering

medRxiv(2022)10.1101/2022.11.03.22281471

N/A

0.208DataRank · unranked

3 citations

Muhammad Hashim Raza, Tae‐Un Han, Terra D. Barnes, Philip Shaw, Gustavo Sudre +4 more

Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

Genes(2020)10.3390/genes11101122

N/A

0DataRank · unranked

20 citations

Iván A. López, Cristina Fenollar‐Ferrer, Rabia Faridi, Claudio Anselmi, Asma Ali Khan +10 more

Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient mice

Research Square(2023)10.21203/rs.3.rs-3310464/v1

N/A

0DataRank · unranked

0 citations

Rizwan Yousaf, Sayaka Inagaki, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell +9 more

Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly

Communications Biology(2024)10.1038/s42003-024-06466-1

N/A

0DataRank · unranked

12 citations

Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen +17 more

Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome

Clinical Genetics(2024)10.1111/cge.14514

N/A

0DataRank · unranked

6 citations

Pamela Stratton, Noemi Salmeri, Robert J. Morell, Asma Ali Khan, Muhammad A. Usmani +4 more

Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1-Deficient Mice

Genes(2024)10.3390/genes15070845

N/A

0DataRank · unranked

2 citations

Rizwan Yousaf, Sayaka Inagaki, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell +9 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

KLHL13 functional defects cause neurodevelopmental disorder in humans that can be rescued via inhibition of AURKB in cellular and animal models

Genetics in Medicine(2025)10.1016/j.gim.2025.101625

N/A

0DataRank · unranked

0 citations

Zubair M. Ahmed, Yaping Ji, Axel Schmidt, Meron Azage, María Palomares‐Bralo +10 more

Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F

Molecular Therapy(2023)10.1016/j.ymthe.2023.10.017

N/A

0DataRank · unranked

15 citations

Saumil Sethna, Todd Duncan, Muhammad Azhar Naeem, T. Michael Redmond, Sheikh Riazuddin +4 more

New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder

Human Genetics(2021)10.1007/s00439-021-02319-7

N/A

0DataRank · unranked

52 citations

Alessandro Rea, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, Shoujun Gu, Zunaira Munir +7 more

CIB2 regulates mTORC1 signaling and is essential for autophagy and visual function

Nature Communications(2021)10.1038/s41467-021-24056-1

N/A

0DataRank · unranked

49 citations

Patrick A. Scott, Arnaud P. J. Giese, Todd Duncan, Xiaoying Jian, Sheikh Riazuddin +6 more

Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disability

European Journal of Human Genetics(2021)10.1038/s41431-021-00968-w

N/A

0DataRank · unranked

11 citations

Faiza Rasheed, Muhammad Rashid, Hans van Bokhoven, Zubair M. Ahmed, Sheikh Riazuddin +2 more