Gulshan Karbani

4.5k total citations · 1 hit paper
18 papers, 2.6k citations indexed

About

Gulshan Karbani is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Gulshan Karbani has authored 18 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Gulshan Karbani's work include Microtubule and mitosis dynamics (5 papers), Congenital limb and hand anomalies (4 papers) and Mitochondrial Function and Pathology (3 papers). Gulshan Karbani is often cited by papers focused on Microtubule and mitosis dynamics (5 papers), Congenital limb and hand anomalies (4 papers) and Mitochondrial Function and Pathology (3 papers). Gulshan Karbani collaborates with scholars based in United Kingdom, United Arab Emirates and United States. Gulshan Karbani's co-authors include C. Geoffrey Woods, Emma Roberts, Hussain Jafri, Kelly Springell, James J. Cox, Duncan P. McHale, Lihadh Al‐Gazali, Adeline K. Nicholas, Daniel J. Hampshire and John N. Wood and has published in prestigious journals such as Nature, Nature Genetics and Cancer.

In The Last Decade

Gulshan Karbani

18 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An SCN9A channelopathy causes congenital inability to experience pain

2006 1.1k citations James J. Cox, Frank Reimann et al. Nature profile →

Peers

Countries citing papers authored by Gulshan Karbani

Since Specialization

Citations

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

Fields of papers citing papers by Gulshan Karbani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gulshan Karbani

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Culture, attitude and knowledge about breast cancer and preventive measures: a qualitative study of South Asian breast cancer patients in the UK. 2011 ·PubMed ·Gulshan Karbani, Jennifer N. W. Lim, Jenny Hewison, Karl Atkin, Kieran Horgan, Mark Lansdown, Carol Chu	60
2	The molecular landscape of ASPM mutations in primary microcephaly 2008 ·Journal of Medical Genetics ·Adeline K. Nicholas, Eric A. Swanson, James J. Cox, Gulshan Karbani, (unknown), Kelly Springell, Daniel J. Hampshire, M Ahmed, Jacquelyn Bond, Daniela Benedetto, Marco Fichera, Corrado Romano, William B. Dobyns, C. Geoffrey Woods	68
3	An SCN9A channelopathy causes congenital inability to experience pain breakdown → 2006 ·Nature ·James J. Cox, Frank Reimann, Adeline K. Nicholas, (unknown), Emma Roberts, Kelly Springell, Gulshan Karbani, Hussain Jafri, (unknown), Yasmin Raashid, Lihadh Al‐Gazali, (unknown), Enza Maria Valente, Shaun Gorman, Richard Williams, Duncan P. McHale, John N. Wood, Fiona M. Gribble, C. Geoffrey Woods	1094
4	Quantification of Homozygosity in Consanguineous Individuals with Autosomal Recessive Disease 2006 ·The American Journal of Human Genetics ·C. Geoffrey Woods, James J. Cox, Kelly Springell, Daniel J. Hampshire, Moin Mohamed, Martin McKibbin, Rowena Stern, F. Lucy Raymond, Richard Sandford, Saghira Malik Sharif, Gulshan Karbani, (unknown), Jacquelyn Bond, David Clayton, Chris F. Inglehearn	192
5	Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome 2006 ·The American Journal of Human Genetics ·C. Geoffrey Woods, Sigmar Stricker, Petra Seemann, Rowena Stern, James J. Cox, (unknown), Emma Roberts, Kelly Springell, Simon Scott, Gulshan Karbani, Saghira Malik Sharif, Carmel Toomes, Jacquelyn Bond, Dheeraj Kumar, Lihadh Al‐Gazali, Stefan Mundlos	116
6	A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size 2005 ·Nature Genetics ·Jacquelyn Bond, Emma Roberts, Kelly Springell, (unknown), (unknown), J. William Higgins, Daniel J. Hampshire, Ewan E. Morrison, (unknown), Elias O. Silva, (unknown), Diana Baralle, Michela Raponi, Gulshan Karbani, Yasmin Abdul Rashid, Hussain Jafri, Christopher Bennett, Peter Corry, Christopher A. Walsh, C. Geoffrey Woods	423
7	Natural history of cardiac involvement in geleophysic dysplasia 2004 ·American Journal of Medical Genetics Part A ·A. J. Scott, Sonia N. Yeung, D F Dickinson, Gulshan Karbani, Yanick J. Crow	14
8	Cancer by negative heterosis: breast and ovarian cancer excess in hybrids of inbred ethnic groups 2004 ·Medical Hypotheses ·Srdjan Denic, (unknown), Manal Awad, Gulshan Karbani, (unknown)	5
9	Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain 2002 ·The American Journal of Human Genetics ·Andrew P. Jackson, (unknown), Sandra Bell, Jimi Adu, Carmel Toomes, Ian Carr, Emma Roberts, Daniel J. Hampshire, Yanick J. Crow, Alan J. Mighell, Gulshan Karbani, Hussain Jafri, Yasmin Abdul Rashid, Robert F. Mueller, Alexander F. Markham, C. Geoffrey Woods	340
10	A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34 2000 ·The American Journal of Human Genetics ·Leanne Moynihan, Andrew P. Jackson, Emma Roberts, Gulshan Karbani, Ian Lewis, Peter Corry, G Turner, Robert F. Mueller, Nicholas Lench, C. Geoffrey Woods	81
11	Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter 1998 ·The American Journal of Human Genetics ·Andrew P. Jackson, Duncan P. McHale, David A. Campbell, Hussain Jafri, Yasmin Abdul Rashid, (unknown), Gulshan Karbani, Peter Corry, Malcolm I. Levene, Robert F. Mueller, (unknown), Nicholas Lench, C. Geoffrey Woods	117
12	Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: a possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild. 1997 ·PubMed ·(unknown), (unknown), R F Mueller, Gulshan Karbani	16
13	A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22. 1997 ·Journal of Medical Genetics ·David A. Campbell, Duncan P. McHale, Kathryn Brown, Leanne Moynihan, Mark Houseman, Gulshan Karbani, G. Parry, (unknown), Valerie Newton, (unknown), Alex Markham, Nicholas Lench, R F Mueller	31
14	Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: A possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al‐Awadi, and Raas‐Rothschild 1997 ·American Journal of Medical Genetics ·Durgesh Kumar, (unknown), R F Mueller, Gulshan Karbani	1
15	Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: A possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild 1997 ·American Journal of Medical Genetics ·(unknown), (unknown), R F Mueller, Gulshan Karbani	14
16	Linkage Studies of Non-Syndromic Recessive Deafness (NSRD) in a Family Originating from the Mirpur Region of Pakistan Maps DFNB1 Centromeric to D13S175 1996 ·Human Molecular Genetics ·Kathryn Brown, (unknown), Gulshan Karbani, G. Parry, (unknown), Gillian P. Crockford, D. Timothy Bishop, Valerie Newton, A.F. Markham, R F Mueller	37
17	Familial microcephaly with normal intelligence in a patient with acute lymphoblastic leukemia 1992 ·Cancer ·David Heney, (unknown), G Turner, Gulshan Karbani, Jacquès Cadranel, Ian Lewis, C. C. Bailey	5
18	Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay. 1991 ·Archives of Disease in Childhood ·N. Shaw, David Haigh, (unknown), Gulshan Karbani, J T Brocklebank, Michael J. Dillon	22

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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