Naseebullah Kakar

1.0k total citations
27 papers, 377 citations indexed

About

Naseebullah Kakar is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Naseebullah Kakar has authored 27 papers receiving a total of 377 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 3 papers in Genetics. Recurrent topics in Naseebullah Kakar's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Naseebullah Kakar is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Naseebullah Kakar collaborates with scholars based in Pakistan, Germany and United States. Naseebullah Kakar's co-authors include Jamil Ahmad, Christian Kubisch, Guntram Borck, Tadahiko Yamamoto, Richard J. Bing, Ingrid Goebel, Paul Johnson, Peter Nürnberg, Ernest R. Vina and Adeel Ahmad and has published in prestigious journals such as Scientific Reports, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Naseebullah Kakar

26 papers receiving 364 citations

Peers

Naseebullah Kakar

GENET

EPIDE

HEPAT

Patrizia Annunziata Italy

Christine Broissand France

Jane L. Ko United States

Mark Moffat United States

H Klein Germany

Katherine Dick United States

Cheng‐Da Hsu Taiwan

J. Szpirer Belgium

Maria M Campos United States

C. D. Logsdon Australia

Patrizia Annunziata Italy

Naseebullah Kakar

191 ×1.0

77 ×0.5

GENET

112 ×2.2

EPIDE

48 ×1.1

15 ×0.4

HEPAT

Citations per year, relative to Naseebullah Kakar Naseebullah Kakar (= 1×) peers Patrizia Annunziata

Countries citing papers authored by Naseebullah Kakar

Since Specialization

Citations

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

Fields of papers citing papers by Naseebullah Kakar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naseebullah Kakar

This figure shows the co-authorship network connecting the top 25 collaborators of Naseebullah Kakar. A scholar is included among the top collaborators of Naseebullah Kakar 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 Naseebullah Kakar. Naseebullah Kakar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kakar, Naseebullah, Gandham SriLakshmi Bhavani, Manisha Goyal, et al.. (2024). Multi‐gene panel sequencing in highly consanguineous families and patients with congenital forms of skeletal dysplasias. Clinical Genetics. 106(1). 47–55. 1 indexed citations

Kakar, Naseebullah, Asmat Ali, Nathalie Kruse, et al.. (2024). Further evidence of biallelic NAV3 variants associated with recessive neurodevelopmental disorder with dysmorphism, developmental delay, intellectual disability, and behavioral abnormalities. Human Genetics. 144(1). 55–65.

Pozojevic, Jelena, Joanne Trinh, Naseebullah Kakar, et al.. (2024). LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome. Scientific Reports. 14(1). 16302–16302. 2 indexed citations

Rehman, Zia Ur, Sher Alam Khan, Samin Jan, et al.. (2023). Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms. Frontiers in Neurology. 14. 1168307–1168307. 5 indexed citations

Parveen, Asia, et al.. (2023). A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani family. Human Genome Variation. 10(1). 16–16. 2 indexed citations

Hashem, Mais, Rüstem Yilmaz, Muddathir H. Hamad, et al.. (2017). Mutations of PTPN23 in developmental and epileptic encephalopathy. Human Genetics. 136(11-12). 1455–1461. 13 indexed citations

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

Désir, Julie, Naseebullah Kakar, Thomas D. Mueller, et al.. (2015). A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia. Orphanet Journal of Rare Diseases. 10(1). 84–84. 16 indexed citations

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

10.

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

11.

Szakszon, Katalin, Carmelo Salpietro, Naseebullah Kakar, et al.. (2013). De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say‐Barber/Biesecker/Young‐Simpson syndrome. American Journal of Medical Genetics Part A. 161(4). 884–888. 26 indexed citations

12.

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

13.

Baloch, Abdul Hameed, Muneer Ahmed, Adeel Ahmad, et al.. (2012). Various Aspects, Patterns and Risk Factors in Breast Cancer Patients of Balochistan. Asian Pacific Journal of Cancer Prevention. 13(8). 4013–4016. 11 indexed citations

14.

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

15.

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

16.

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

17.

Naeem, Muhammad, et al.. (2008). Prevalence of hepatitis C virus (HCV) genotypes in Balochistan. Molecular Biology Reports. 36(6). 1511–1514. 37 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.

Yamamoto, Tadahiko, Naseebullah Kakar, Ernest R. Vina, Paul Johnson, & Richard J. Bing. (2000). The effect of aspirin and two nitric oxide donors on the infarcted heart in situ. Life Sciences. 67(7). 839–846. 26 indexed citations

20.

Yamamoto, Tadahiko, et al.. (1999). Production of Prostanoids and Nitric Oxide by Infarcted Heartin Situand the Effect of Aspirin. Biochemical and Biophysical Research Communications. 257(2). 488–493. 18 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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