Sayedul Haque

1.2k total citations
33 papers, 863 citations indexed

About

Sayedul Haque is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Sayedul Haque has authored 33 papers receiving a total of 863 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Developmental Biology. Recurrent topics in Sayedul Haque's work include Congenital limb and hand anomalies (8 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers) and RNA regulation and disease (6 papers). Sayedul Haque is often cited by papers focused on Congenital limb and hand anomalies (8 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers) and RNA regulation and disease (6 papers). Sayedul Haque collaborates with scholars based in Pakistan, United States and Canada. Sayedul Haque's co-authors include Wasim Ahmad, Mahmud Ahmad, M. Siddique, Daniel H. Cohn, Hasan Abbas, Deborah Krakow, Muhammad Faiyaz‐Ul‐Haque, Mahmud Ahmad, Muhammad Faiyaz ul Haque and Sajid Malik and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Sayedul Haque

32 papers receiving 833 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sayedul Haque Pakistan 15 503 273 209 196 167 33 863
Kenji Naritomi Japan 17 400 0.8× 463 1.7× 10 0.0× 65 0.3× 28 0.2× 58 689
Patricia Ybot‐González Spain 21 973 1.9× 239 0.9× 15 0.1× 373 1.9× 4 0.0× 39 1.4k
Nisha Patel Saudi Arabia 17 428 0.9× 267 1.0× 7 0.0× 69 0.4× 11 0.1× 39 727
Pauline Terhal Netherlands 18 574 1.1× 632 2.3× 6 0.0× 79 0.4× 10 0.1× 28 1.0k
Shih‐hsin Kan United States 15 415 0.8× 337 1.2× 4 0.0× 106 0.5× 99 0.6× 47 873
Peter S. Budd United Kingdom 10 374 0.7× 156 0.6× 61 0.3× 426 2.2× 6 0.0× 18 740
Shelagh Joss United Kingdom 13 303 0.6× 169 0.6× 7 0.0× 43 0.2× 13 0.1× 19 452
Lucie Dupuis Canada 13 243 0.5× 335 1.2× 5 0.0× 92 0.5× 5 0.0× 28 554
María Begoña Cachón-González United Kingdom 11 425 0.8× 160 0.6× 102 0.5× 277 1.4× 19 896
Cristina‐Maria Cruciat Germany 7 1.2k 2.4× 203 0.7× 18 0.1× 124 0.6× 2 0.0× 8 1.4k

Countries citing papers authored by Sayedul Haque

Since Specialization
Citations

This map shows the geographic impact of Sayedul Haque's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sayedul Haque with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sayedul Haque more than expected).

Fields of papers citing papers by Sayedul Haque

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sayedul Haque. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sayedul Haque. The network helps show where Sayedul Haque may publish in the future.

Co-authorship network of co-authors of Sayedul Haque

This figure shows the co-authorship network connecting the top 25 collaborators of Sayedul Haque. A scholar is included among the top collaborators of Sayedul Haque based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sayedul Haque. Sayedul Haque is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dar, Ahsana, et al.. (2019). Cytotoxic and genotoxic action of Tagetes patula flower methanol extract and patuletin using the Allium test. TURKISH JOURNAL OF BIOLOGY. 43(5). 326–339. 5 indexed citations
2.
VanderMeer, Julia E., et al.. (2012). A novel ZRS mutation in a Balochi tribal family with triphalangeal thumb, pre‐axial polydactyly, post‐axial polydactyly, and syndactyly. American Journal of Medical Genetics Part A. 158A(8). 2031–2035. 12 indexed citations
3.
Shah, Afzal, et al.. (2008). Electrochemical and Spectroscopic Investigations of Protonated Ferrocene-DNA Intercalation. Analytical Sciences. 24(11). 1437–1441. 49 indexed citations
4.
Malik, Sajid, Katta M. Girisha, Muhammad Wajid, et al.. (2007). Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences. BMC Medical Genetics. 8(1). 78–78. 16 indexed citations
5.
Rafiq, Muhammad, Sajid Malik, Muhammad Sohail, et al.. (2005). A Novel Locus of Ectodermal Dysplasia Maps to Chromosome 10q24.32–q25.1. Journal of Investigative Dermatology. 124(2). 338–342. 7 indexed citations
6.
Irshad, Saba, et al.. (2005). Localization of a novel autosomal recessive non‐syndromic hearing impairment locus DFNB55 to chromosome 4q12‐q13.2. Clinical Genetics. 68(3). 262–267. 8 indexed citations
7.
Wajid, Muhammad, Maria H. Chahrour, Sayedul Haque, et al.. (2005). A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3. American Journal of Medical Genetics Part A. 133A(1). 18–22. 14 indexed citations
8.
Ansar, Muhammad, Muhammad Aminuddin, Maqsood Anwar, et al.. (2004). Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1‐17q25.3. Clinical Genetics. 66(1). 73–78. 3 indexed citations
9.
Ansar, Muhammad, Maria H. Chahrour, Muhammad Imran Arshad, et al.. (2004). DFNB44, a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus, Maps to Chromosome 7p14.1-q11.22. Human Heredity. 57(4). 195–199. 10 indexed citations
10.
Faiyaz‐Ul‐Haque, Muhammad, Sayedul Haque, M. PATEL, et al.. (2004). Fine mapping of the X‐linked split‐hand/split‐foot malformation (SHFM2) locus to a 5.1‐Mb region on Xq26.3 and analysis of candidate genes. Clinical Genetics. 67(1). 93–97. 42 indexed citations
11.
Arshad, Muhammad Imran, et al.. (2003). A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1–14q24.3 in large consanguineous kindred from Pakistan. European Journal of Human Genetics. 11(1). 77–80. 20 indexed citations
12.
Malik, Sajid, Muhammad Imran Arshad, Muhammad Aminuddin, et al.. (2003). A novel type of autosomal recessive syndactyly: Clinical and molecular studies in a family of Pakistani origin. American Journal of Medical Genetics Part A. 126A(1). 61–67. 16 indexed citations
13.
Wajid, Muhammad, Amir Ali Abbasi, Kai Yan, et al.. (2003). DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22–q21.12. European Journal of Human Genetics. 11(10). 812–815. 9 indexed citations
14.
Faiyaz‐Ul‐Haque, Muhammad, Wasim Ahmad, Abdul Wahab, et al.. (2002). Frameshift mutation in the cartilage‐derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe‐type chondrodysplasia. American Journal of Medical Genetics. 111(1). 31–37. 48 indexed citations
15.
16.
Jamal, Syed M., Sajid Malik, Wasim Ahmad, Sayedul Haque, & Habib Ahmad. (2001). Brothers No Longer Sisters: Case Study of Pseudohermaphrodites. Journal of Medical Sciences(Faisalabad). 1(2). 55–57.
17.
Nöthen, Markus M., Sven Cichon, Ina R. Vogt, et al.. (1998). A Gene for Universal Congenital Alopecia Maps to Chromosome 8p21-22. The American Journal of Human Genetics. 62(2). 386–390. 46 indexed citations
18.
Cichon, Sven, Ina R. Vogt, Axel M. Hillmer, et al.. (1998). Cloning, Genomic Organization, Alternative Transcripts and Mutational Analysis of the Gene Responsible for Autosomal Recessive Universal Congenital Alopecia. Human Molecular Genetics. 7(11). 1671–1679. 114 indexed citations
19.
Ahmad, Mahmud, Hasan Abbas, & Sayedul Haque. (1993). Alopecia universalis as a single abnormality in an inbred Pakistani kindred. American Journal of Medical Genetics. 46(4). 369–371. 21 indexed citations
20.
Ahmad, Mahmud, et al.. (1990). Fibular hypoplasia and complex brachydactyly (Du Pan Syndrome) in an inbred Pakistani kindred. American Journal of Medical Genetics. 36(3). 292–296. 11 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kenji Naritomi Breakdown of academic impact, for papers by Patricia Ybot‐González Breakdown of academic impact, for papers by Nisha Patel Breakdown of academic impact, for papers by Pauline Terhal Breakdown of academic impact, for papers by Shih‐hsin Kan Breakdown of academic impact, for papers by Peter S. Budd Breakdown of academic impact, for papers by Shelagh Joss Breakdown of academic impact, for papers by Lucie Dupuis Breakdown of academic impact, for papers by María Begoña Cachón-González Breakdown of academic impact, for papers by Cristina‐Maria Cruciat
Rankless by CCL
2026