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American Journal of Human Genetics|March 11, 2000
An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locusJ B Vincent, M L Neves-Pereira, A D Paterson, et al.
Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
Bulletin Du Cancer|August 29, 2006
Challenges in the stratification of breast tumors for tailored therapiesJ-P Thiery, X Sastre-Garau, B Vincent-Salomon, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2006
Sequence variants within exon 1 of MECP2 occur in females with mental retardationChris G Harvey, Sailesh D Menon, Beata Stachowiak, et al.
Plos Neglected Tropical Diseases|May 1, 2018
Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcerQuentin B Vincent, Aziz Belkadi, Cindy Fayard, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 30, 2021
Genome-wide association study of suicidal behaviour severity in mood disordersClement C Zai, Chiara Fabbri, Georgina M Hosang, et al.
Human Genetics|September 1, 2019
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimatesQing Ouyang, Brian C Kavanaugh, Lena Joesch-Cohen, et al.
Nature Communications|July 30, 2024
The bearing capacity of asteroid (65803) Didymos estimated from boulder tracksJ Bigot, P Lombardo, N Murdoch, et al.
BMC Medical Genetics|January 7, 2014
Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1Wei Xu, Sarah Cohen-Woods, Qian Chen, et al.
American Journal of Human Genetics|September 13, 2016
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic FeaturesAnide Johansen, Rasim O Rosti, Damir Musaev, et al.
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