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Clara Lajonchere | Researchclopedia

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Clara Lajonchere

APLA Health ORCID

72

Works

9,733

Citations

33

h-index

43

i10-index

Research Topics

Autism Spectrum Disorder Research Genomics and Rare Diseases Genomic variations and chromosomal abnormalities

Affiliations

Autism Speaks2009–2015

University of Southern California2007–2015

University of Iowa2012–2012

Allen Institute for Brain Science2012–2012

APLA Health2025–2025

Top Works

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

Dalila Pinto,Alistair T. Pagnamenta,et al.

20102,042 citations

Genetics and Neurodevelopmental Disorders

Ethics in Clinical Research

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Péter Szatmári,Ping G. Tepper,et al.

20071,388 citations

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Kai Wang,Haitao Zhang,et al.

2009970 citations

Microduplications of 16p11.2 are associated with schizophrenia

Shane McCarthy,Vladimir Makarov,et al.

2009732 citations

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

Richard Anney,Lambertus Klei,et al.

2010588 citations

Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

Yong‐hui Jiang,Ryan K. C. Yuen,et al.

2013496 citations

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

Maja Bućan,Brett S. Abrahams,et al.

2009432 citations

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

Richard Anney,Lambertus Klei,et al.

2012375 citations

A unified genetic theory for sporadic and inherited autism

Xiaoyue Zhao,Anthony Leotta,et al.

2007325 citations