| 1 |
Mapping Chromosomal Loci in Specific Language Impairment: A Pedigree-Focused Approach
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| 2 |
Global genetic differentiation of complex traits shaped by natural selection in humans.
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In: Nature communications, vol. 9, no. 1, pp. 1865 (2018)
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| 3 |
A Mitochondrial Statigraphy for Island Southeast Asia
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In: American Journal of Human Genetics (2015)
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| 4 |
A Mitochondrial Statigraphy for Island Southeast Asia
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In: American Journal of Human Genetics (2015)
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| 5 |
Reconstructing Austronesian population history in Island Southeast Asia.
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In: Nature communications, vol 5, iss 1 (2014)
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| 6 |
New insight on the Xq28 association with systemic sclerosis.
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In: Ann Rheum Dis , 72 (12) 2032 - 2038. (2013) (2013)
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| 7 |
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity
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In: ISSN: 1018-4813 ; European Journal of Human Genetics, Vol. 21, No 6 (2013) pp. 659-65 (2013)
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| 8 |
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool.
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In: Am J Hum Genet , 91 (1) 83 - 96. (2012) (2012)
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| 9 |
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.
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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 (2011)
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| 10 |
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.
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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 (2010)
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| 12 |
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
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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 (2009)
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| 13 |
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.
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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 (2008)
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| 14 |
The co-evolution of culturally inherited altruistic helping and cultural transmission under random group formation.
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In: Theoretical Population Biology, vol. 73, no. 4, pp. 506-516 (2008)
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| 15 |
The relation between multilocus population genetics and social evolution theory.
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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 (2007)
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| 16 |
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.
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In: ISSN: 1364-6745 ; EISSN: 1364-6753 ; neurogenetics ; https://hal.archives-ouvertes.fr/hal-00281700 ; neurogenetics, Springer Verlag, 2006, 7 (3), pp.149-56. ⟨10.1007/s10048-006-0044-2⟩ (2006)
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| 17 |
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.
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In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 126B, iss 1 (2004)
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| 18 |
Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.
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In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; ORA review team (2004)
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| 19 |
An unusual case of X-linked adrenoleukodystrophy with auditory processing difficulties as the first and sole clinical manifestation.
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In: J Am Acad Audiol , 15 (2) pp. 152-160. (2004) (2004)
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| 20 |
Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits.
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In: Cytogenetic and genome research, vol 98, iss 4 (2002)
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