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Prevalence of amyloid‐β pathology in distinct variants of primary progressive aphasia
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In: ISSN: 0364-5134 ; EISSN: 1531-8249 ; Annals of Neurology ; https://hal-univ-fcomte.archives-ouvertes.fr/hal-03630161 ; Annals of Neurology, Wiley, 2018, 84 (5), pp.729-740. ⟨10.1002/ana.25333⟩ (2018)
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| 3 |
Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis.
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In: Human molecular genetics, vol 27, iss 24 (2018)
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| 4 |
Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.
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In: Genetics in medicine, vol. 20, no. 7, pp. 778-784 (2018)
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A Neolithic expansion, but strong genetic structure, in the independent history of New Guinea. ...
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| 7 |
A Neolithic expansion, but strong genetic structure, in the independent history of New Guinea
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| 8 |
Global Genomic Epidemiology of Salmonella enterica Serovar Typhimurium DT104.
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In: ISSN: 0099-2240 ; EISSN: 1098-5336 ; Applied and Environmental Microbiology ; https://hal-pasteur.archives-ouvertes.fr/pasteur-01421019 ; Applied and Environmental Microbiology, American Society for Microbiology, 2016, 82 (8), pp.2516-26. ⟨10.1128/AEM.03821-15⟩ (2016)
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| 9 |
Fine-Scale Human Population Structure in Southern Africa Reflects Ecogeographic Boundaries.
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In: Genetics, vol 204, iss 1 (2016)
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| 10 |
APOE Genotype and Cognitive Functioning in a Large Age-Stratified Population Sample.
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In: Neuropsychology (2016)
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| 11 |
APOE Genotype and Cognitive Functioning in a Large Age-Stratified Population Sample.
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In: Neuropsychology (2016)
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Towards a Integrated Evolutionary Model to Study Evolution of Evolution
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In: EvoEvo Workshop (Satellite workshop of ECAL 2015) ; https://hal.inria.fr/hal-01252796 ; EvoEvo Workshop (Satellite workshop of ECAL 2015), Jul 2015, York, United Kingdom (2015)
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| 13 |
Establishment of a successful assessment and treatment service for Australian prison inmates with chronic hepatitis C
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In: Medical Journal of Australia (2015)
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| 14 |
Darwin, artificial selection, and poverty
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In: Politics and the Life Sciences (2015)
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| 15 |
Aspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome
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In: Research outputs 2014 to 2021 (2015)
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| 16 |
Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population.
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In: Invest Ophthalmol Vis Sci , 56 (13) pp. 8297-8305. (2015) (2015)
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| 17 |
Aspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome
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| 18 |
Reconstructing Austronesian population history in Island Southeast Asia.
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In: Nature communications, vol 5, iss 1 (2014)
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| 19 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
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In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014)
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| 20 |
Phenotype and genotype in 101 males with X-linked creatine transporter deficiency
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