Ghazala Mirza - Concepedia

Author

Ghazala Mirza

Centre for Human Genetics

Also Known As

G Mirza, G. K. Mirza, G. MIRZA, G. Mirza, Ghazala K Mirza, Ghazala K. Mirza, Ghazala Mirza, Mirza, Ghazala

Publications

8.6K

Citations

H-Index

Concepts

All Affiliations

Centre for Human Genetics University of Oxford King's College London Guy's Hospital Inserm

About

Ghazala Mirza is an author at Centre for Human Genetics specializing in genetics, medicine, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	978
2	Natural Sciences	1	1	36
3	Biostatistics	1	1	2K
4	Cell Biology	1	1	58
5	Diabetes	1	1	420

Ghazala Mirza

Publications

5.5K

Citations

H-Index

Page 1

	Year	Citations
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data Stefano Colella, Christopher Yau, Jennifer M. Taylor, Nucleic Acids Research	2007	617
A genome-wide scan for common alleles affecting risk for autism Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2010	585
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci Kyle J. Gaulton, Teresa Ferreira, Yeji Lee, Nature Genetics Genome-wide Association StudyGenetic DeterminantGenotype-phenotype AssociationGenetic Fine MappingGenetics	2015	420
Individual common variants exert weak effects on the risk for autism spectrum disorders Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2012	372
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder Jillian P. Casey, Tiago R. Magalhães, Judith Conroy, Human Genetics	2011	200
Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia Alistair T. Pagnamenta, Elena Bacchelli, Maretha Jonge, Biological Psychiatry	2010	141
A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data Christopher Yau, Dmitri Mouradov, Robert N. Jorissen, Genome biology	2010	138
Longitudinal assessment of sputum microbiome by sequencing of the 16S rRNA gene in non-cystic fibrosis bronchiectasis patients Michael J. Cox, Elena Turek, Catherine Hennessy, PLoS ONE	2017	134
Delineation of two distinct 6p deletion syndromes Angela Davies, Ghazala Mirza, Gurbax S. Sekhon, Human Genetics Down SyndromeMendelian DisorderGenetic DisorderGeneticsPathology	1999	113

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