Concepedia

12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech

Julien Thévenon, Patrick Callier, Joris Andrieux, Bruno Delobel, Albert David, Sylvie Sukno, Delphine Minot, Laure Mosca Anne, Nathalie Marle, Damien Sanlaville,

European Journal of Human Genetics · 2012 · 106 citations · 35 references

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35

Prevalence of Specific Language Impairment in Kindergarten Children

J. Bruce Tomblin, Nancy L. Records, Paula Buckwalter et al. · Journal of Speech Language and Hearing Research · 1997 · 2.3K citations

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A forkhead-domain gene is mutated in a severe speech and language disorder

Cecilia Lai, Simon E. Fisher, Jane A. Hurst et al. · Nature · 2001 · 2.1K citations · Full text

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

Brian J. O’Roak, Pelagia Deriziotis, Choli Lee et al. · Nature Genetics · 2011 · 1.2K citations · Full text

, , +14

A Functional Genetic Link between Distinct Developmental Language Disorders

Sonja C. Vernes, Dianne F. Newbury, Brett S. Abrahams et al. · New England Journal of Medicine · 2008 · 691 citations · Full text

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The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

E.K. Green, Detelina Grozeva, Ian Jones et al. · Molecular Psychiatry · 2009 · 532 citations · Full text

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