G. Mirza

发表

Functional impact of global rare copy number variation in autism spectrum disorders

Gary D Bader, Joseph T. Glessner, Stephen J. Guter, 2010, Nature.

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

C. Yau, G. Mirza, J. Ragoussis, 2007, Nucleic acids research.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Ayellet V. Segrè, 2012, Nature Genetics.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants

Enrico Petretto, Gareth Ball, Alka Saxena, 2017, Nature Communications.

“Integrative genomics study of microglial transcriptome reveals effect of DLG4 (PSD95) on white matter in preterm infants”

G. Mirza, E. Petretto, G. Ball, 2017, bioRxiv.

A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data

Oliver Sieber, Christopher Yau, Jiannis Ragoussis, 2010, Genome Biology.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Tanya M. Teslovich, Andrew D. Johnson, Kyle J. Gaulton, 2014, Nature Genetics.

Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Christian Gieger, Jason Carey, Steven Wiltshire, 2016 .

Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

Jiannis Ragoussis, Ernesto Lowy, Alistair T. Pagnamenta, 2010, Biological Psychiatry.

Machine learning shows association between genetic variability in PPARG and cerebral connectivity in preterm infants

Joseph V. Hajnal, Paul Aljabar, Giovanni Montana, 2017, Proceedings of the National Academy of Sciences.

Human epidermal differentiation complex in a single 2.5 Mbp long continuum of overlapping DNA cloned in bacteria integrating physical and transcript maps.

G. Mirza, J. Ragoussis, D. Nižetić, 1999, The Journal of investigative dermatology.

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.

Steve D. M. Brown, Jennifer R. Davies, G. Mirza, 2005, Proceedings of the National Academy of Sciences of the United States of America.

An interstitial deletion of 6p24-p25 proximal to theFKHL7 locus and includingAP-2α that affects anterior eye chamber development.

G. Mirza, J. Ragoussis, A. Davies, 1999, Journal of medical genetics.

An interstitial deletion of 6 p 24p 25 proximal to the FKHL 7 locus and including AP-2 á that a V ects anterior eye chamber development

G. Mirza, J. Ragoussis, A. Davies, 1999 .

Edinburgh Research Explorer Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants

G. Mirza, E. Petretto, G. Ball, 2017 .

Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies

G. Mirza, J. Ragoussis, M. Farrall, 2009, Human mutation.

De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder

A. Pagnamenta, G. Mirza, J. Parr, 2014, Journal of Medical Genetics.

haracterization of a Family with Rare Deletions in NTNAP5 and DOCK4 Suggests Novel Risk Loci for utism and Dyslexia

P. Deloukas, R. Ophoff, M. Nöthen, 2022 .

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Joseph T. Glessner, Stephen J. Guter, D. Pinto, 2011, Human Genetics.

Molecular cloning, chromosomal mapping, and developmental expression of a novel protein tyrosine phosphatase-like gene.

K L Thornburg, J Ragoussis, G. Mirza, 1999, Genomics.

Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region

J. Ragoussis, G. Mirza, J. Ragoussis, 2004, Cytogenetic and Genome Research.

Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes

G. Mirza, J. Ragoussis, R. Newbury-Ecob, 2004, European Journal of Human Genetics.

Delineation of two distinct 6p deletion syndromes

G. Mirza, J. Ragoussis, F. Speleman, 1999, Human Genetics.

Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting.

G. Mirza, J. Ragoussis, Y. Kuroki, 1998, Journal of medical genetics.

Schizophrenia in an adult with 6p25 deletion syndrome

G. Mirza, J. Ragoussis, A. Bassett, 2006, American journal of medical genetics. Part A.

Molecularly defined interstitial tandem duplication 6p case with mild manifestations.

G. Mirza, J. Ragoussis, C. Turner, 2001, American journal of medical genetics.

Comparison of human chromosome 6p25 with mouse chromosome 13 reveals a greatly expanded ov-serpin gene repertoire in the mouse.

G. Mirza, J. Ragoussis, P. Denny, 2002, Genomics.

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

G. Mirza, J. Ragoussis, P. Bird, 1998, Cytogenetic and Genome Research.

Partial trisomy 22 in a liveborn resulting from a rearrangement between chromosomes 6 and 22

G. Mirza, J. Ragoussis, K. Imaizumi, 2000, Journal of medical genetics.

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population

G. Mirza, A. Monaco, D. Newbury, 2011, European Journal of Human Genetics.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Tanya M. Teslovich, Andrew D. Johnson, Kyle J. Gaulton, 2014 .

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Simon C. Potter, 2012, Nature Genetics.

Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Tanya M. Teslovich, Kyle J. Gaulton, Sara M. Willems, 2015, Nature Genetics.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Stephen J. Guter, D. Pinto, S. Scherer, 2011, Human Genetics.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Ross M. Fraser, 2012, Nature Genetics.

A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data

C. Yau, G. Mirza, J. Ragoussis, 2010, Genome Biology.