Jamil Ahmad

1.5k total citations
25 papers, 407 citations indexed

About

Jamil Ahmad is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Jamil Ahmad has authored 25 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Neurology. Recurrent topics in Jamil Ahmad's work include Hearing, Cochlea, Tinnitus, Genetics (3 papers), RNA regulation and disease (3 papers) and Neurological diseases and metabolism (2 papers). Jamil Ahmad is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (3 papers), RNA regulation and disease (3 papers) and Neurological diseases and metabolism (2 papers). Jamil Ahmad collaborates with scholars based in Pakistan, Germany and United States. Jamil Ahmad's co-authors include Naseebullah Kakar, Christian Kubisch, Guntram Borck, Sheikh Riazuddin, Nancy J. Cox, Dennis Drayna, Naveeda Riaz, Anna Pluzhnikov, Stacy Steinberg and Ingrid Goebel and has published in prestigious journals such as The American Journal of Human Genetics, Human Genetics and European Journal of Human Genetics.

In The Last Decade

Jamil Ahmad

24 papers receiving 385 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jamil Ahmad Pakistan 13 169 133 64 64 47 25 407
Rinat Gizatullin Sweden 18 441 2.6× 95 0.7× 60 0.9× 40 0.6× 2 0.0× 37 750
Anne Maddalena United States 17 411 2.4× 736 5.5× 61 1.0× 26 0.4× 27 0.6× 27 1.1k
Jesse Ingels United States 11 242 1.4× 104 0.8× 4 0.1× 31 0.5× 3 0.1× 14 566
Susan Zeesman Canada 12 315 1.9× 284 2.1× 12 0.2× 42 0.7× 44 0.9× 19 608
Tiffany Vu United States 8 341 2.0× 469 3.5× 17 0.3× 20 0.3× 70 1.5× 9 691
Sureni V. Mullegama United States 15 315 1.9× 308 2.3× 11 0.2× 30 0.5× 8 0.2× 27 564
Vera Beyer Germany 9 181 1.1× 168 1.3× 11 0.2× 20 0.3× 15 0.3× 15 318
Robin Ryther United States 12 463 2.7× 336 2.5× 68 1.1× 18 0.3× 19 850
J. Arp Canada 12 85 0.5× 21 0.2× 41 0.6× 6 0.1× 5 0.1× 16 626
Stuart I. Davidson United Kingdom 7 162 1.0× 221 1.7× 49 0.8× 6 0.1× 7 685

Countries citing papers authored by Jamil Ahmad

Since Specialization
Citations

This map shows the geographic impact of Jamil Ahmad'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 Jamil Ahmad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jamil Ahmad more than expected).

Fields of papers citing papers by Jamil Ahmad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jamil Ahmad. 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 Jamil Ahmad. The network helps show where Jamil Ahmad may publish in the future.

Co-authorship network of co-authors of Jamil Ahmad

This figure shows the co-authorship network connecting the top 25 collaborators of Jamil Ahmad. A scholar is included among the top collaborators of Jamil Ahmad 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 Jamil Ahmad. Jamil Ahmad 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.
Kakar, Naseebullah, Denise Horn, Eva L. Decker, et al.. (2017). Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophies. American Journal of Medical Genetics Part A. 176(2). 438–442. 8 indexed citations
2.
Kakar, Muhammad Azam, et al.. (2016). Multiplex One-step RT-PCR for Detection and Serotyping of Foot and Mouth Disease Virus in Balochistan. 5(2). 74–80. 1 indexed citations
3.
Ullah, Asad, Syed M. Jamal, Aurore Romey, et al.. (2016). Genetic Characterization of Serotypes A and Asia-1 Foot-and-mouth Disease Viruses in Balochistan, Pakistan, in 2011. Transboundary and Emerging Diseases. 64(5). 1569–1578. 24 indexed citations
4.
Kakar, Naseebullah, Ingrid Goebel, Tahir Yaqub, et al.. (2016). Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17(3-4). 260–265. 10 indexed citations
5.
Kakar, Naseebullah, Jamil Ahmad, Déborah Morris-Rosendahl, et al.. (2014). STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly. Human Genetics. 134(1). 45–51. 26 indexed citations
6.
Baloch, Abdul Hameed, Muhammad Muzzamil Luqman, Adeel Ahmad, et al.. (2014). Missense mutations (p.H371Y, p.D438Y) in gene CHEK2 are associated with breast cancer risk in women of Balochistan origin. Molecular Biology Reports. 41(2). 1103–1107. 14 indexed citations
7.
Akhtar, Tanveer, Allah Rakha, Ghazanfar Abbas, et al.. (2014). Genetic characterization of the Makrani people of Pakistan from mitochondrial DNA control-region data. Legal Medicine. 17(2). 134–139. 15 indexed citations
8.
Kakar, Naseebullah, Jamil Ahmad, Christian Kubisch, & Guntram Borck. (2013). Exon skipping and severe childhood‐onset obesity caused by a leptin receptor mutation. American Journal of Medical Genetics Part A. 161(10). 2672–2674. 11 indexed citations
9.
Ahmad, Jamil, et al.. (2013). Linkage study of DFNB3 responsible for hearing loss in human. Indian journal of human genetics. 19(3). 325–325. 2 indexed citations
10.
Graul‐Neumann, Luitgard, Ulrike Wille, Naseebullah Kakar, et al.. (2013). Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe. European Journal of Human Genetics. 22(6). 726–733. 19 indexed citations
11.
Kakar, Naseebullah, Ingrid Goebel, Gudrun Nürnberg, et al.. (2012). A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly. European Journal of Medical Genetics. 55(12). 727–731. 34 indexed citations
12.
Ali, Zafar, et al.. (2012). The study of gene GJB2/DFNB1 causing deafness in humans by linkage analysis from district Peshawar. Indian journal of human genetics. 18(2). 217–217. 1 indexed citations
13.
Kakar, Naseebullah, Adeel Ahmad, Abdul Hameed Baloch, et al.. (2012). A missense mutation (p.G274R) in gene ASPA causes Canavan disease in a Pakistani family. Molecular Biology Reports. 39(5). 6197–6201. 5 indexed citations
14.
Borck, Guntram, Naseebullah Kakar, Katrin Friedrich, et al.. (2011). An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group. Human Genetics. 131(2). 209–216. 16 indexed citations
15.
Kakar, Naseebullah, et al.. (2010). Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from Pakistan. Clinical Genetics. 78(3). 247–256. 18 indexed citations
16.
Naeem, Muhammad, et al.. (2008). Prevalence of hepatitis C virus (HCV) genotypes in Balochistan. Molecular Biology Reports. 36(6). 1511–1514. 37 indexed citations
17.
Farid, A., Bernhard F. Benkel, Jamil Ahmad, et al.. (2008). Genetic variability at seven codons of the prion protein gene in nine Pakistani sheep breeds. Journal of Genetics. 87(2). 187–190. 7 indexed citations
18.
Goebel, Ingrid, et al.. (2008). A novel HSF4gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan. BMC Medical Genetics. 9(1). 99–99. 34 indexed citations
19.
Ahmad, Jamil, Shaheen N. Khan, Shahid Y. Khan, et al.. (2005). DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1. Human Genetics. 116(5). 407–412. 12 indexed citations
20.
Riaz, Naveeda, Stacy Steinberg, Jamil Ahmad, et al.. (2005). Genomewide Significant Linkage to Stuttering on Chromosome 12. The American Journal of Human Genetics. 76(4). 647–651. 77 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.

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