Author

Nuala Sykes

Observed names: N H Sykes, Nuala H Sykes, Nuala H. Sykes, Sykes, Nuala H

Observed institutions: Centre for Human Genetics, University of Oxford

OpenAlex ID: A5111549537

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

2010 · Dalila Pinto, Alistair T. Pagnamenta, et al. · Nature · 1,994

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

2007 · Peter Szatmari, Ann P Thompson, et al. · Nature Genetics · 1,398

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Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

2005 · Kay D. MacDermot, Elena Bonora, et al. · The American Journal of Human Genetics · 406

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

2012 · Richard Anney, Lambertus Klei, et al. · Human Molecular Genetics · 370

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

2011 · Jillian P. Casey, Tiago Magalhaes, et al. · Human Genetics · 196

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Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT

2005 · Gabrielle Barnby, Aaron Abbott, et al. · The American Journal of Human Genetics · 178

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

2009 · IMGSAC, E Maestrini, et al. · Molecular Psychiatry · 142

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MET and autism susceptibility: family and case–control studies

2008 · Inês Sousa, Taane G Clark, et al. · European Journal of Human Genetics · 90

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Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

2004 · Elena Bonora, Janine A Lamb, et al. · European Journal of Human Genetics · 81

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection

2009 · Nuala H Sykes, Claudio Toma, et al. · European Journal of Human Genetics · 69

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Autism: the quest for the genes

2007 · Nuala H. Sykes, Janine A. Lamb · Expert Reviews in Molecular Medicine · 58

CNVs leading to fusion transcripts in individuals with autism spectrum disorder

2012 · Richard Holt, Nuala H Sykes, et al. · European Journal of Human Genetics · 34

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A novel family with an unusual early‐onset generalized dystonia

2004 · Giovanni Fabbrini, Francesco Brancati, et al. · Movement Disorders · 15

A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus

2006 · Elena Bacchelli, Francesco Blasi, et al. · American Journal of Medical Genetics Part A · 1

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

2010 · Richard Anney, Lambertus Klei, et al. · Newcastle University ePrints (Newcastle Univesity)

High-density SNP association study of the autism susceptibility loci on chromosome 7q

2006 · Nuala Sykes, Janine A. Lamb, et al. · American Journal of Medical Genetics Part A

Identification of foxp2 truncation as a novel cause of developmental speech disorder.

2004 · K D MacDermot, Elena Bonora, et al. · UCL Discovery (University College London)

Works count: 22

Citation count: 5,032

H-index: 13

I10-index: 13