Sadaf Naz

ORCID: 0000-0002-1912-0235

Also affiliated with University of Sindh, Long Island University, University of the Punjab, University of Karachi, Hazara University, Liaquat National Hospital, NYU Grossman Long Island School of Medicine, Texas A&M University

NeuroscienceBiochemistry, 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 9 papers. Top paper: “Variants of human CLDN9 cause mild to profound hearing loss”.

Variants of human CLDN9 cause mild to profound hearing loss

Human Mutation(2021)10.1002/humu.24260

N/A

0.476DataRank · unranked

6 citations

Christophe Philippe, Inna A. Belyantseva, Yoko Nakano, Cristina Fenollar‐Ferrer, Risa Tona +19 more

Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder

Brain(2024)10.1093/brain/awae363

N/A

0.104DataRank · unranked

1 citations

Elisa Calì, Reza Maroofian, Maha S. Zaki, Alistair T. Pagnamenta, Zafar Ali +51 more

RGS3 and IL1RAPL1 missense variants implicate defective neurotransmission in early-onset inherited schizophrenias

Journal of Psychiatry and Neuroscience(2022)10.1503/jpn.220070

N/A

0DataRank · unranked

13 citations

José V. Pardo, Sadaf Naz, Ambreen Kanwal

Preliminary studies on apparent mendelian psychotic disorders in consanguineous families

BMC Psychiatry(2022)10.1186/s12888-022-04304-4

N/A

0DataRank · unranked

4 citations

Sohail A. Sheikh, Amina Iftikhar, Sadaf Naz, José V. Pardo, Ambreen Kanwal

PKHD1L1 , A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss

medRxiv(2023)10.1101/2023.10.08.23296081

N/A

0DataRank · unranked

3 citations

Pedro De‐la‐Torre, Mina Zamani, Hanjun Wang, Hina Khan, T. Morris +12 more

Rare Homozygous Variants in INSR and NFXL1 Are Associated with Severe Treatment-Resistant Psychosis

International Journal of Molecular Sciences(2025)10.3390/ijms26104925

N/A

0DataRank · unranked

1 citations

Rimsha Zulfiqar, Husnain Arshad Cheema, Nauman Jabbar, Amina Iftikhar, Alexander Butt +4 more

Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan

Scientific Reports(2020)10.1038/s41598-020-68779-5

N/A

0DataRank · unranked

15 citations

Rasheeda Bashir, Midhat Salman, Ghulam Mujtaba, Nara Sobreira, P. Dane Witmer +2 more

A truncated CDC14A retains catalytic structure and phosphatase activity preserving male fertility but causes nonsyndromic deafness

Journal of Biological Chemistry(2025)10.1016/j.jbc.2025.110982

N/A

0DataRank · unranked

0 citations

Gina Jackisch, Inna A. Belyantseva, Muhammad Imran, Sadaf Naz, Céleste Sèle +6 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