Accueil > News / événements > Autisme > Publications
Publications
PUBLICATIONS, CONFERENCES, POSTERS
Autism
Author(s) |
Date |
Title |
Type |
Origin |
Liens |
||||||||
| Carayol J, Schellenberg GD, Dombroski B, Genin E, Rousseau F, Dawson G. |
Oct. 2011 |
Autism risk assesment in siblings of affected children using sex-specific genetic scores |
article | Molecular Autism |
 |
||||||||
| May 2011 | Converging Evidence for an Association of ATP2B2 Allelic Variants with Autism in Male Subjects | article |
Biological Psychiatry |
|
|||||||||
| Persico AM, Lombardi F, Rousseau F, Palmieri L. | Oct 2010 | SLC25A12 gene variants confer protection from autism | oral presentation |
IX International congress Autism Europe (Italy) | |
||||||||
| Sacco R, Rousseau F, Lewin P, Persico A. | Oct 2010 | ITGB3 gene variants double the risk of autism | Poster | IX International congress Autism Europe (Italy) | |
||||||||
| Lepagnol-Bestel AM, Moalic JM, Hager J, Simonneau MJ. |
May 2010 |
Constructing a Transgenic Mouse Model Based On SLC25A12, MARK1 and PRKCB1 Gene Dosage Imbalance Mimicking Gene Expression Changes Found in Brain of ASD Patients |
abstract/poster | IMFAR (Philadelphia) |
 |
||||||||
| Carayol J, Schellenberg J, Tores F, Hager J, Ziegler A, Dawson G. | Feb 2010 | Assessing the impact of a combinated analysis of 4 common low-risk genetic variants on autism risk | article | Molecular Autism | |
 |
|||||||
| Hager J,Carayol J, Tores F, Rousseau F, Hall SB, Persico AM. | Oct. 2009 | A Combination of Common Low Risk Genetic Variants allows the Identification of a Group of Individuals at Higher Risk of Developing Autism | abstract/poster | AACAP (Hawaï) | |
||||||||
| Persico AM, Lombardi F, Sacco R, Rousseau F, Lewin P, Scarcia P, Palmieri L. | Oct. 2009 | Protective gene variants in unaffected siblings of autistic individuals | abstract / oral presentation | SfN (Chicago) | |
||||||||
| Lintas C, Sacco R, Lombardi F, Altieri L, Curatolo P, Manzi B, Alessandrelli R, Militerni R, Bravaccio C, Lenti C, Saccani M, Rousseau F, Hager J, Persico AM. | Oct. 2009 | Family-based candidate gene studies in autism spectrum disorders | abstract/poster | SfN (Chicago) | |
||||||||
| Hager J. | May. 2009 | Association study of a linkage region on chromosome 3p25 in 816 families shows strong evidence for association of ATP2B2 with autism and language delay | abstract / oral presentation | IMFAR (Chicago) | |
||||||||
| Hager J, Carayol J, Tores F, Letexier M, Lindenbaum P, Rousseau F. | Apr. 2009 | Association of variants of PITX1 with specific endo-phenotypes of autism spectrum disorder. | abstract/poster | IRIA (Tours) | |
||||||||
| Hager J. | Nov. 2008 | Combining information from candidate genes for autism improves predictive power | abstract/poster | SHG (Philadelphie) | |
||||||||
| Tores F. | Oct. 2008 | A risk assessment test for autism in siblings in high risk families based on multiples genes : clinical assessment and potential application | abstract/poster | Genova Autism Asssociation (Toronto) | |
||||||||
| Dawson G, Schellenberg GD, Ziegler A, Koenig IR, Rousseau F, Carayol J, Korvatska O, Munson J, Estes A, Yu CE, Hager J. | Oct. 2008 | A multi-gene risk assessment test for autism in siblings in high-risk families with an already affected first child : clinical assessment and potential applications | abstract/oral presentation | AAP NCE (Boston) | |
||||||||
| Hager J. | Oct. 2008 | Association of the PITX1 gene with autism and specific sub-phenotypes og the autism spectrum disorder | abstract/oral presentation | Autism Neuroscience Conference (London) | |
||||||||
| L Palmieri, V Papaleo, V Porcelli, P Scarcia, L Gaita, R Sacco, J Hager, F Rousseau, P Curatolo, B Manzi, R Militerni, C Bravaccio, S Trillo, C Schneider, R Melmed, M Elia, C Lenti, M Saccani, T Pascucci, S Puglisi-Allegra, K-L Reichelt and A M Persico. | July 2008 | Altered calcium homeostatis in autism-spectrum disorders: evidence from biochemical end genetic studies of the mitochondrial aspartate/glutamate carrier AGC1 |
article advance online publication |
Molecular Psychiatry | |
|
|||||||
| Maussion G, Carayol J, Lepagnol-Bestel AM, Tores F, Loe-Mie Y, Milbreta U, Rousseau F, Fontaine K, Renaud J, Moalic JM, Philippi A, Chedotal A, Gorwood P, Ramoz N, Hager J, Simonneau M. | 2008 | Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism | article | "Human Molecular Genetics"" | |
|
|||||||
| Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J. | Dec. 2007 | Association of autism with polymorphisms in the paired-like homeodomain transcrption factor 1 (PITX1) on chromosome 5q31 : a candidate gene analysis | article | "BMC Medical Genetics" | |
|
|||||||
| Hager J. | 2007 | IntegraTest TM Autism Development of a multi-gene risk assessment test | abstract/oral presentation | Molecular Diagnostics Conference (Philadelphie) | |
||||||||
| Sacco R, Papaleo Y, Hager J, Rousseau F, Moessner R, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Curatolo P, Manzi B, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM. | Mar. 2007 | Case-control and family-based association studies of candidates genes in autistic disorder and its endophenotypes : THP2 and GLO1 | article | "BMC Medical Genetics" | |
|
|||||||
| Philippi A, Roschmann E, Tores F, Lindenbaum P, Benajou A, Germain-Leclerc L, Marcaillou C, Fontaine K, Vanpeene M, Roy S, Maillard S, Decaulne V, Saraiva JP, Brooks P, Rousseau F, Hager J. | Oct. 2005 | Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism | article | "Molecular Psychiatry" | |
|
|||||||
Statistics
Author(s) |
Date |
Title |
Type |
Origin |
Liens |
||||||||
| Carayol J, Tores F, König I, Hager J, Ziegler A. | May 2009 | Evaluating diagnostic accuracy of genetic profiles in affected offspring families | article |
Accepted for publication in "Statistics in Medicine 2010" |
|
||||||||
| Carayol J, Philippi A, Tores F. | 2006 | Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment. | article | "Genetic Epidemiology" | |
|
|||||||
| Franke D, Philippi A, Tores F, Ziegler A, König IR. | Sept. 2005 | On confidence intervals for genotype relative risks and attributable risks from case parent trio designs for candidate-gene studies | article | "Human Heredity" | |
|
|||||||
Methods
Author(s) |
Date |
Title |
Type |
Origin |
Liens |
||||||||
| Brooks P, Marcaillou C, Vanpeene M, Saraiva JP, Stockholm D, Francke S, Favis R, Cohen N, Rousseau F, Tores F, Lindenbaum P, Hager J, Philippi A. | Mar. 2009 | Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta | article | "BMC Genetics" | |
|
|||||||