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Claudio Toma - Publications

Affiliations: 
University of Barcelona, Barcelona, Cataluña, Spain 
 Centro Biologia Molecular Severo Ochoa Universidad Autonoma Madrid 
Area:
Human Genetics
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56 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Koromina M, Ravi A, Panagiotaropoulou G, Schilder BM, Humphrey J, Braun A, Bidgeli T, Chatzinakos C, Coombes B, Kim J, Liu X, Terao C, O 'Connell KS, Adams M, Adolfsson R, ... ... Toma C, et al. Fine-mapping genomic loci refines bipolar disorder risk genes. Medrxiv : the Preprint Server For Health Sciences. PMID 38405768 DOI: 10.1101/2024.02.12.24302716  0.648
2023 Ollà I, Pardiñas AF, Parras A, Hernández IH, Santos-Galindo M, Picó S, Callado LF, Elorza A, Rodríguez-López C, Fernández-Miranda G, Belloc E, Walters JTR, O'Donovan MC, Méndez R, Toma C, et al. Pathogenic mis-splicing of CPEB4 in schizophrenia. Biological Psychiatry. PMID 36958377 DOI: 10.1016/j.biopsych.2023.03.010  0.381
2023 Zwicker A, Fullerton JM, Mullins N, Rice F, Hafeman DM, van Haren NEM, Setiaman N, Merranko JA, Goldstein BI, Ferrera AG, Stapp EK, de la Serna E, Moreno D, Sugranyes G, Herrero SM, ... ... Toma C, et al. Polygenic Scores and Onset of Major Mood or Psychotic Disorders Among Offspring of Affected Parents. The American Journal of Psychiatry. appiajp20220476. PMID 36856707 DOI: 10.1176/appi.ajp.20220476  0.702
2022 Hesam-Shariati S, Overs BJ, Roberts G, Toma C, Watkeys OJ, Green MJ, Pierce KD, Edenberg HJ, Wilcox HC, Stapp EK, McInnis MG, Hulvershorn LA, Nurnberger JI, Schofield PR, Mitchell PB, et al. Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder. Translational Psychiatry. 12: 310. PMID 35922419 DOI: 10.1038/s41398-022-02079-6  0.725
2021 Overs BJ, Roberts G, Ridgway K, Toma C, Hadzi-Pavlovic D, Wilcox HC, Hulvershorn LA, Nurnberger JI, Schofield PR, Mitchell PB, Fullerton JM. Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 34726322 DOI: 10.1002/ajmg.b.32879  0.68
2021 Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als TD, Bigdeli TB, Børte S, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars SP, Ikeda M, ... ... Toma C, et al. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics. PMID 34002096 DOI: 10.1038/s41588-021-00857-4  0.761
2021 Toma C, Shaw AD, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21. Journal of Psychiatry & Neuroscience : Jpn. 46: E247-E257. PMID 33729739 DOI: 10.1503/jpn.200083  0.747
2021 Overs BJ, Lenroot RK, Roberts G, Green MJ, Toma C, Hadzi-Pavlovic D, Pierce KD, Schofield PR, Mitchell PB, Fullerton JM. Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder. Psychiatry Research. Neuroimaging. 309: 111258. PMID 33529975 DOI: 10.1016/j.pscychresns.2021.111258  0.695
2020 Jamshidi J, Williams LM, Schofield PR, Park HRP, Montalto A, Chilver MR, Bryant RA, Toma C, Fullerton JM, Gatt JM. Diverse phenotypic measurements of wellbeing: Heritability, temporal stability, and the variance explained by polygenic scores. Genes, Brain, and Behavior. e12694. PMID 32785990 DOI: 10.1111/Gbb.12694  0.588
2020 Torrico B, Antón-Galindo E, Fernàndez-Castillo N, Rojo-Francàs E, Ghorbani S, Pineda-Cirera L, Hervás A, Rueda I, Moreno E, Fullerton JM, Casadó V, Buitelaar JK, Rommelse N, Franke B, Reif A, ... ... Toma C, et al. Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses. Journal of Clinical Medicine. 9. PMID 32545830 DOI: 10.3390/Jcm9061851  0.82
2020 Toma C, Shaw AD, Overs BJ, Mitchell PB, Schofield PR, Cooper AA, Fullerton JM. De Novo Gene Variants and Familial Bipolar Disorder. Jama Network Open. 3: e203382. PMID 32383744 DOI: 10.1001/jamanetworkopen.2020.3382  0.76
2020 Putt S, Yanes T, Meiser B, Kaur R, Fullerton JM, Barlow-Stewart K, Schofield PR, Toma C, Peay H, Mitchell PB. Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder. Journal of Affective Disorders. 265: 342-350. PMID 32090758 DOI: 10.1016/J.Jad.2020.01.037  0.733
2020 Toma C. Genetic Variation across Phenotypic Severity of Autism. Trends in Genetics : Tig. PMID 32037010 DOI: 10.1016/J.Tig.2020.01.005  0.449
2019 Toma C, Díaz-Gay M, Soares de Lima Y, Arnau-Collell C, Franch-Expósito S, Muñoz J, Overs B, Bonjoch L, Carballal S, Ocaña T, Cuatrecasas M, Díaz de Bustamante A, Castells A, Bujanda L, Cubiella J, et al. Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing. Clinical and Translational Gastroenterology. PMID 31703024 DOI: 10.14309/ctg.0000000000000100  0.385
2019 Toma C, Díaz-Gay M, Soares de Lima Y, Arnau-Collell C, Franch-Expósito S, Muñoz J, Overs B, Bonjoch L, Carballal S, Ocaña T, Cuatrecasas M, Díaz de Bustamante A, Castells A, Bujanda L, Cubiella J, et al. Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing. Clinical and Translational Gastroenterology. 10: e00100. PMID 31663907 DOI: 10.14309/Ctg.0000000000000100  0.694
2019 Toma C, Díaz-Gay M, Franch-Expósito S, Arnau-Collell C, Overs B, Muñoz J, Bonjoch L, Soares de Lima Y, Ocaña T, Cuatrecasas M, Castells A, Bujanda L, Balaguer F, Cubiella J, Caldés T, et al. Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer. International Journal of Cancer. PMID 31525256 DOI: 10.1002/Ijc.32683  0.696
2019 Torrico B, Shaw AD, Mosca R, Vivó-Luque N, Hervás A, Fernàndez-Castillo N, Aloy P, Bayés M, Fullerton JM, Cormand B, Toma C. Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes Journal of Psychiatry & Neuroscience : Jpn. 44: 1-10. PMID 31094488 DOI: 10.1503/Jpn.180184  0.811
2019 Hesam-Shariati S, Overs B, Toma C, Watkeys O, Green M, Roberts G, Leung V, Stuart A, Schofield PR, Mitchell PB, Fullerton J. M49 EPIGENOME-WIDE ASSOCIATION STUDY (EWAS) OF YOUNG PEOPLE WITH FAMILIAL RISK OF BIPOLAR DISORDER European Neuropsychopharmacology. 29: S192. DOI: 10.1016/J.Euroneuro.2019.08.149  0.664
2019 Torrico B, Shaw A, Mosca R, Vivó-Luque N, Hervas A, Fernàndez-Castillo N, Aloy P, Bayés M, Fullerton J, Cormand B, Toma C. F21WHOLE EXOME SEQUENCING IDENTIFIES LRP1 AS NOVEL CANDIDATE GENE ACROSS PSYCHIATRIC DISORDERS European Neuropsychopharmacology. 29: S1120-S1121. DOI: 10.1016/J.Euroneuro.2018.08.101  0.819
2019 Overs BJ, Lenroot RK, Roberts G, Green MJ, Hadzi-Pavlovic D, Frankland A, Levy F, Toma C, Schofield PR, Mitchell PB, Fullerton J. The Relationship Between Functional Dopamine D2 Receptor Haplotypes And Cognitive Outcomes, As Mediated By Regional Brain Structure: A Comparison Of Control, At-Risk, And Bipolar Disorder Subjects European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.375  0.645
2019 Lenroot RK, Overs B, Roberts G, Frankland A, Levy F, Toma C, Wieckert CS, Schofield P, Mitchell P, Fullerton J. Interactive Effects Of Family History, Polygenic Risk And Age On Cortical Thickness In Young People At High Genetic Risk Of Bipolar Disorder European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.256  0.643
2019 Toma C, Shaw AD, Allcock RJ, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. ADDRESSING THE IMPACT OF RARE GENETIC VARIANTS IN EXTENDED/MULTIPLEX BIPOLAR FAMILIES European Neuropsychopharmacology. 29: S837-S838. DOI: 10.1016/J.Euroneuro.2017.08.101  0.654
2019 Shaw A, Toma C, Allcock R, Heath A, Pierce K, Mitchell PB, Schofield P, Fullerton J. COMBINED WHOLE EXOME SEQUENCING AND LINKAGE ANALYSIS REVEALS LINKAGE TO 10Q11-10Q21 LOCUS WHICH IS NOT EXPLAINED BY GWAS-ASSOCIATED SNP OR RARE VARIANTS IN ANK3 European Neuropsychopharmacology. 29: S834-S835. DOI: 10.1016/J.Euroneuro.2017.08.096  0.732
2018 Toma C, Pierce KD, Shaw AD, Heath A, Mitchell PB, Schofield PR, Fullerton JM. Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. Plos Genetics. 14: e1007535. PMID 30586385 DOI: 10.1371/Journal.Pgen.1007535  0.793
2018 Brandler WM, Antaki D, Gujral M, Kleiber ML, Whitney J, Maile MS, Hong O, Chapman TR, Tan S, Tandon P, Pang T, Tang SC, Vaux KK, Yang Y, Harrington E, ... ... Toma C, et al. Paternally inherited cis-regulatory structural variants are associated with autism. Science (New York, N.Y.). 360: 327-331. PMID 29674594 DOI: 10.1126/Science.Aan2261  0.774
2018 Toma C, Shaw AD, Allcock RJN, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. An examination of multiple classes of rare variants in extended families with bipolar disorder. Translational Psychiatry. 8: 65. PMID 29531218 DOI: 10.1038/S41398-018-0113-Y  0.783
2017 Wilcox HC, Fullerton JM, Glowinski AL, Benke K, Kamali M, Hulvershorn LA, Stapp EK, Edenberg HJ, Roberts GMP, Ghaziuddin N, Fisher C, Brucksch C, Frankland A, Toma C, Shaw AD, et al. Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts. Journal of the American Academy of Child and Adolescent Psychiatry. 56: 1073-1080. PMID 29173741 DOI: 10.1016/J.Jaac.2017.09.428  0.697
2017 Sintas C, Carreño O, Fernàndez-Castillo N, Corominas R, Vila-Pueyo M, Toma C, Cuenca-León E, Barroeta I, Roig C, Volpini V, Macaya A, Cormand B. Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia. Scientific Reports. 7: 2514. PMID 28566750 DOI: 10.1038/S41598-017-02554-X  0.732
2017 Arenas C, Toma C, Cormand B, Irigoien I. Identifying Extreme Observations, Outliers and Noise in Clinical and Genetic Data Current Bioinformatics. 12: 101-117. DOI: 10.2174/1574893611666160606161031  0.648
2017 Cormand B, Torrico B, Ghorbani S, Fernàndez-Castillo N, Pineda L, Hervás A, Franke B, Buitelaar J, Freitag C, Reif A, Rueda I, Kleppe R, Haavik J, Toma C. Contribution of The 14-3-3 Gene Family To Autism Spectrum Disorder European Neuropsychopharmacology. 27: S374-S375. DOI: 10.1016/J.Euroneuro.2016.09.404  0.841
2016 Torrico B, Chiocchetti AG, Bacchelli E, Trabetti E, Hervás A, Franke B, Buitelaar JK, Rommelse N, Yousaf A, Duketis E, Freitag CM, Caballero-Andaluz R, Martinez-Mir A, Scholl FG, Ribasés M, ... ... Toma C, et al. Lack of replication of previous autism spectrum disorder GWAS hits in European populations. Autism Research : Official Journal of the International Society For Autism Research. PMID 27417655 DOI: 10.1002/Aur.1662  0.798
2015 Toma C, Torrico B, Hervás A, Salgado M, Rueda I, Valdés-Mas R, Buitelaar JK, Rommelse N, Franke B, Freitag C, Reif A, Pérez-Jurado LA, Battaglia A, Mazzone L, Bacchelli E, et al. Common and rare variants of microRNA genes in autism spectrum disorders. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-11. PMID 25903372 DOI: 10.3109/15622975.2015.1029518  0.803
2015 Torrico B, Fernàndez-Castillo N, Hervás A, Milà M, Salgado M, Rueda I, Buitelaar JK, Rommelse N, Oerlemans AM, Bralten J, Freitag CM, Reif A, Battaglia A, Mazzone L, Maestrini E, ... ... Toma C, et al. Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability. European Journal of Human Genetics : Ejhg. PMID 25782667 DOI: 10.1038/Ejhg.2015.37  0.827
2014 Hervás A, Toma C, Romarís P, Ribasés M, Salgado M, Bayes M, Balmaña N, Cormand B, Maristany M, Guijarro S, Arranz MJ. The involvement of serotonin polymorphisms in autistic spectrum symptomatology. Psychiatric Genetics. 24: 158-63. PMID 24887447 DOI: 10.1097/Ypg.0000000000000034  0.772
2014 Toma C, Torrico B, Hervás A, Valdés-Mas R, Tristán-Noguero A, Padillo V, Maristany M, Salgado M, Arenas C, Puente XS, Bayés M, Cormand B. Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations. Molecular Psychiatry. 19: 784-90. PMID 23999528 DOI: 10.1038/Mp.2013.106  0.838
2013 Carreño O, Corominas R, Serra SA, Sintas C, Fernández-Castillo N, Vila-Pueyo M, Toma C, Gené GG, Pons R, Llaneza M, Sobrido MJ, Grinberg D, Valverde MÁ, Fernández-Fernández JM, Macaya A, et al. Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies. Molecular Genetics & Genomic Medicine. 1: 206-22. PMID 24498617 DOI: 10.1186/1129-2377-14-S1-P26  0.743
2013 Camacho-Garcia RJ, Hervás A, Toma C, Balmaña N, Cormand B, Martinez-Mir A, Scholl FG. Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses. Psychiatric Genetics. 23: 262-6. PMID 24064682 DOI: 10.1097/Ypg.0000000000000013  0.721
2013 Sánchez-Mora C, Ramos-Quiroga JA, Garcia-Martínez I, Fernàndez-Castillo N, Bosch R, Richarte V, Palomar G, Nogueira M, Corrales M, Daigre C, Martínez-Luna N, Grau-Lopez L, Toma C, Cormand B, Roncero C, et al. Evaluation of single nucleotide polymorphisms in the miR-183-96-182 cluster in adulthood attention-deficit and hyperactivity disorder (ADHD) and substance use disorders (SUDs). European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 23: 1463-73. PMID 23906647 DOI: 10.1016/J.Euroneuro.2013.07.002  0.712
2013 Urbizu A, Toma C, Poca MA, Sahuquillo J, Cuenca-León E, Cormand B, Macaya A. Chiari malformation type I: a case-control association study of 58 developmental genes. Plos One. 8: e57241. PMID 23437350 DOI: 10.1371/Journal.Pone.0057241  0.76
2013 Toma C, Hervás A, Torrico B, Balmaña N, Salgado M, Maristany M, Vilella E, Martínez-Leal R, Planelles MI, Cuscó I, del Campo M, Pérez-Jurado LA, Caballero-Andaluz R, de Diego-Otero Y, Pérez-Costillas L, et al. Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2. Psychiatric Genetics. 23: 82-5. PMID 23277129 DOI: 10.1097/Ypg.0B013E32835D6Fc6  0.819
2013 Toma C, Hervás A, Balmaña N, Salgado M, Maristany M, Vilella E, Aguilera F, Orejuela C, Cuscó I, Gallastegui F, Pérez-Jurado LA, Caballero-Andaluz R, Diego-Otero Yd, Guzmán-Alvarez G, Ramos-Quiroga JA, et al. Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 14: 516-27. PMID 22397633 DOI: 10.3109/15622975.2011.602719  0.779
2012 Rodríguez-Pascau L, Toma C, Macías-Vidal J, Cozar M, Cormand B, Lykopoulou L, Coll MJ, Grinberg D, Vilageliu L. Characterisation of two deletions involving NPC1 and flanking genes in Niemann-Pick type C disease patients. Molecular Genetics and Metabolism. 107: 716-20. PMID 23142039 DOI: 10.1016/J.Ymgme.2012.10.004  0.726
2011 Pérez-Dueñas B, Ormazábal A, Toma C, Torrico B, Cormand B, Serrano M, Sierra C, De Grandis E, Marfa MP, García-Cazorla A, Campistol J, Pascual JM, Artuch R. Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspects. Archives of Neurology. 68: 615-21. PMID 21555636 DOI: 10.1001/Archneurol.2011.80  0.789
2011 Ormazabal A, Serrano M, Garcia-Cazorla A, Campistol J, Artuch R, Castro de Castro P, Barredo-Valderrama E, Armstrong J, Toma C, Cormand B. Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 1558-60. PMID 21465550 DOI: 10.1002/Mds.23564  0.705
2011 Toma C, Hervás A, Balmaña N, Vilella E, Aguilera F, Cuscó I, del Campo M, Caballero R, De Diego-Otero Y, Ribasés M, Cormand B, Bayés M. Association study of six candidate genes asymmetrically expressed in the two cerebral hemispheres suggests the involvement of BAIAP2 in autism. Journal of Psychiatric Research. 45: 280-2. PMID 20888579 DOI: 10.1016/J.Jpsychires.2010.09.001  0.72
2010 Pérez-Dueñas B, Toma C, Ormazábal A, Muchart J, Sanmartí F, Bombau G, Serrano M, García-Cazorla A, Cormand B, Artuch R. Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 gene. Journal of Inherited Metabolic Disease. 33: 795-802. PMID 20857335 DOI: 10.1007/S10545-010-9196-1  0.726
2010 Pons R, Serrano M, Ormazabal A, Toma C, Garcia-Cazorla A, Area E, Ribasés M, Kanavakis E, Drakaki K, Giannakopoulos A, Orfanou I, Youroukos S, Cormand B, Artuch R. Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 1086-90. PMID 20198643 DOI: 10.1002/Mds.23002  0.677
2010 Maestrini E, Pagnamenta AT, Lamb JA, Bacchelli E, Sykes NH, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri TS, Minopoli F, Reichert J, Cai G, Buxbaum JD, et al. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Molecular Psychiatry. 15: 954-68. PMID 19401682 DOI: 10.1038/Mp.2009.34  0.785
2009 Sykes NH, Toma C, Wilson N, Volpi EV, Sousa I, Pagnamenta AT, Tancredi R, Battaglia A, Maestrini E, Bailey AJ, Monaco AP. Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. European Journal of Human Genetics : Ejhg. 17: 1347-53. PMID 19384346 DOI: 10.1038/Ejhg.2009.47  0.782
2009 Sousa I, Clark TG, Toma C, Kobayashi K, Choma M, Holt R, Sykes NH, Lamb JA, Bailey AJ, Battaglia A, Maestrini E, Monaco AP. MET and autism susceptibility: family and case-control studies. European Journal of Human Genetics : Ejhg. 17: 749-58. PMID 19002214 DOI: 10.1038/Ejhg.2008.215  0.79
2008 Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsäter H, Rastam M, et al. Analysis of X chromosome inactivation in autism spectrum disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 830-5. PMID 18361425 DOI: 10.1002/Ajmg.B.30688  0.726
2008 Velayos-Baeza A, Toma C, Paracchini S, Monaco AP. The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. Human Molecular Genetics. 17: 859-71. PMID 18063668 DOI: 10.1093/Hmg/Ddm358  0.764
2007 Toma C, Rossi M, Sousa I, Blasi F, Bacchelli E, Alen R, Vanhala R, Monaco AP, Järvelä I, Maestrini E. Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations. Molecular Psychiatry. 12: 977-9. PMID 17957233 DOI: 10.1038/Sj.Mp.4002069  0.764
2007 Velayos-Baeza A, Toma C, da Roza S, Paracchini S, Monaco AP. Alternative splicing in the dyslexia-associated gene KIAA0319. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 627-34. PMID 17846832 DOI: 10.1007/S00335-007-9051-3  0.794
2007 Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Toma C, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985  0.764
2006 Blasi F, Bacchelli E, Carone S, Toma C, Monaco AP, Bailey AJ, Maestrini E. SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. European Journal of Human Genetics : Ejhg. 14: 123-6. PMID 16205742 DOI: 10.1038/Sj.Ejhg.5201444  0.778
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