Ghazala Mirza

8.6k total citations
20 papers, 1.1k citations indexed

About

Ghazala Mirza is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Ghazala Mirza has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Ghazala Mirza's work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Advanced biosensing and bioanalysis techniques (2 papers). Ghazala Mirza is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Advanced biosensing and bioanalysis techniques (2 papers). Ghazala Mirza collaborates with scholars based in United Kingdom, United States and Australia. Ghazala Mirza's co-authors include Jiannis Ragoussis, Christopher Yau, Stefano Colella, Chris Holmes, Anne S. Bassett, Penny Clouston, Helen Butler, A Seller, Jennifer M. Taylor and Frances Flinter and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

In The Last Decade

Ghazala Mirza

19 papers receiving 1.1k citations

Peers

Countries citing papers authored by Ghazala Mirza

Since Specialization

Citations

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

Fields of papers citing papers by Ghazala Mirza

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ghazala Mirza

This figure shows the co-authorship network connecting the top 25 collaborators of Ghazala Mirza. A scholar is included among the top collaborators of Ghazala Mirza 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 Ghazala Mirza. Ghazala Mirza 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

#	Work	Indexed citations
1	Longitudinal assessment of sputum microbiome by sequencing of the 16S rRNA gene in non-cystic fibrosis bronchiectasis patients 2017 ·PLoS ONE ·Michael J. Cox, (unknown), (unknown), Ghazala Mirza, Phillip James, Meg Coleman, Andrew Jones, Robert Wilson, Diana Bilton, William Cookson, Miriam F. Moffatt, Michael R. Loebinger	86
2	Machine learning shows association between genetic variability in PPARG and cerebral connectivity in preterm infants 2017 ·Proceedings of the National Academy of Sciences ·Michelle L. Krishnan, Zi Wang, Paul Aljabar, Gareth Ball, Ghazala Mirza, Alka Saxena, Serena J. Counsell, Joseph V. Hajnal, Giovanni Montana, A. David Edwards	24
3	Whole Exome Sequencing of Flow Purified Tumour Cells Reveals Recurrently Mutated Genes and Pathways in Adult T-Cell Lymphoma/Leukaemia (ATLL) 2015 ·Blood ·Richard Dillon, Lucy Cook, Alka Saxena, Rosamond Nuamah, Ghazala Mirza, (unknown), Michael A. Simpson, Sean Whittaker, Charles R. M. Bangham, Graham P. Taylor, Paul Fields	1
4	De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder 2014 ·Journal of Medical Genetics ·Christian Babbs, (unknown), Alistair T. Pagnamenta, Stephen R.F. Twigg, Jonathan Green, Simon J. McGowan, Ghazala Mirza, (unknown), Vikram Sharma, Emanuela V. Volpi, Veronica J. Buckle, Steven A. Wall, Samantha J.L. Knight, Jeremy Parr, Andrew O.M. Wilkie	23
5	Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population 2011 ·European Journal of Human Genetics ·(unknown), Dianne F. Newbury, Lilian Jara, (unknown), Ghazala Mirza, Hernán Palomino, (unknown), Jean‐Baptiste Cazier, Anthony P. Monaco	40
6	A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data 2010 ·Genome biology ·Christopher Yau, Dmitri Mouradov, Robert N. Jorissen, Stefano Colella, Ghazala Mirza, Graham Steers, Adrian L. Harris, Jiannis Ragoussis, Oliver M. Sieber, Chris Holmes	93
7	Seeing clearly: the dominant and recessive nature ofFOXE3in eye developmental anomalies 2009 ·Human Mutation ·Sı̇bel Aylı̇n Uğur İşerı̇, Robert J. Osborne, Martin Farrall, Alexander W. Wyatt, Ghazala Mirza, Gudrun Nürnberg, (unknown), H. Herbert, Angela Martin, Muhammad Sajid Hussain, J. R. O. Collin, Mark Lathrop, Peter Nürnberg, Jiannis Ragoussis, Nicola Ragge	67
8	QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data 2007 ·Nucleic Acids Research ·Stefano Colella, Christopher Yau, Jennifer M. Taylor, Ghazala Mirza, Helen Butler, Penny Clouston, Anne S. Bassett, A Seller, Chris Holmes, Jiannis Ragoussis	400
9	Schizophrenia in an adult with 6p25 deletion syndrome 2006 ·American Journal of Medical Genetics Part A ·Oana Caluseriu, Ghazala Mirza, Jiannis Ragoussis, Eva W. C. Chow, Duncan J. MacCrimmon, Anne S. Bassett	23
10	Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes 2004 ·European Journal of Human Genetics ·Ghazala Mirza, Ruth Williams, (unknown), Robin D. Clark, Ruth Newbury‐Ecob, Shari Baldinger, Frances Flinter, Jiannis Ragoussis	43
11	Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region 2004 ·Cytogenetic and Genome Research ·S. J. Davies, Carol A. Wise, Byrappa Venkatesh, Ghazala Mirza, Andrew Jefferson, Emanuela V. Volpi, Jiannis Ragoussis	25
12	Comparison of Human Chromosome 6p25 with Mouse Chromosome 13 Reveals a Greatly Expanded Ov-Serpin Gene Repertoire in the Mouse 2002 ·Genomics ·Dion Kaiserman, (unknown), Katrina L. Scarff, (unknown), Ghazala Mirza, (unknown), Richard McKeone, Paul Denny, Jessica Cooley, Charaf Benarafa, Eileen Remold‐O’Donnell, Jiannis Ragoussis, Phillip I. Bird	50
13	Molecularly defined interstitial tandem duplication 6p case with mild manifestations 2001 ·American Journal of Medical Genetics ·(unknown), Philip N. Mowrey, Jiannis Ragoussis, Ghazala Mirza, (unknown), (unknown), Clesson Turner, Sondra W. Levin	18
14	Molecular Cloning, Chromosomal Mapping, and Developmental Expression of a Novel Protein Tyrosine Phosphatase-like Gene 1999 ·Genomics ·Dafe Uwanogho, Zoë Hardcastle, (unknown), Ghazala Mirza, Kent L. Thornburg, Jiannis Ragoussis, Paul T. Sharpe	27
15	Delineation of two distinct 6p deletion syndromes 1999 ·Human Genetics ·Angela Davies, Ghazala Mirza, Gurbax S. Sekhon, Peter D. Turnpenny, (unknown), Frank Speleman, (unknown), Nicole Van Regemorter, Esther Vamos, Frances Flinter, Jiannis Ragoussis	88
16	An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development. 1999 ·PubMed ·Angela Davies, Ghazala Mirza, Frances Flinter, (unknown)	48
17	A serpin gene cluster on human chromosome 6p25 contains PI6, PI9 and ELANH2 which have a common structure almost identical to the 18q21 ovalbumin serpin genes 1998 ·Cytogenetic and Genome Research ·Jie Sun, Richard Stephens, Ghazala Mirza, Haruhiko Kanai, Jiannis Ragoussis, Phillip I. Bird	17
18	Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting. 1998 ·Journal of Medical Genetics ·Angela Davies, K Imaizumi, Ghazala Mirza, Richard S. Stephens, Y. Kuroki, (unknown), Jiannis Ragoussis	22
19	A FISH probe specific for the telomeric region of 6p 1997 ·Cytogenetic and Genome Research ·Ghazala Mirza, Angela Davies, Jiannis Ragoussis	0
20	Postoperative endophthalmitis caused by an Enterobacter species 1994 ·Journal of Hospital Infection ·Ghazala Mirza	19

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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