Advances in autism genetics: on the threshold of a new neurobiology

Autism is a heterogeneous syndrome defined by impairments in three core domains: social interaction, language and range of interests. Recent work has led to the identification of several autism susceptibility genes and an increased appreciation of the contribution of de novo and inherited copy number variation. Promising strategies are also being applied to identify common genetic risk variants. Systems biology approaches, including array-based expression profiling, are poised to provide additional insights into this group of disorders, in which heterogeneity, both genetic and phenotypic, is emerging as a dominant theme.

[1]  K. Kohn,et al.  X-ray induced DNA double strand break production and repair in mammalian cells as measured by neutral filter elution. , 1979, Nucleic acids research.

[2]  B. Durkacz,et al.  (ADP-ribose)n participates in DNA excision repair , 1980, Nature.

[3]  B. Durkacz,et al.  The effect of inhibition of (ADP-ribose)n biosynthesis on DNA repair assayed by the nucleoid technique. , 1981, European journal of biochemistry.

[4]  P. Mandel,et al.  Poly(ADP-ribosyl)ation of polynucleosomes causes relaxation of chromatin structure. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[5]  M. James,et al.  Role of poly(adenosine diphosphate ribose) in deoxyribonucleic acid repair in human fibroblasts. , 1982, Biochemistry.

[6]  A. Lehmann,et al.  Poly(ADP-ribosylation) reduces the steady-state level of breaks in DNA following treatment of human cells with alkylating agents. , 1984, Carcinogenesis.

[7]  C. Gillberg,et al.  Frequency of the fragile X syndrome in infantile autism , 1985, Clinical genetics.

[8]  L. Sklar,et al.  Hydrogen peroxide-induced injury of cells and its prevention by inhibitors of poly(ADP-ribose) polymerase. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[9]  F. Althaus,et al.  Release of core DNA from nucleosomal core particles following (ADP-ribose)n-modification in vitro. , 1987, Biochemical and biophysical research communications.

[10]  F. Andermann,et al.  Ataxia—ocular motor aprilaxia: A syndrome mimicking ataxia‐telangiectasia , 1988 .

[11]  C. Gillberg,et al.  A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. , 1989, Journal of child psychology and psychiatry, and allied disciplines.

[12]  C. Bendixen,et al.  Camptothecin-stabilized topoisomerase I-DNA adducts cause premature termination of transcription. , 1990, Biochemistry.

[13]  B. Demple,et al.  Two distinct human DNA diesterases that hydrolyze 3'-blocking deoxyribose fragments from oxidized DNA. , 1991, Nucleic acids research.

[14]  B J Freeman,et al.  Complex segregation analysis of autism. , 1991, American journal of human genetics.

[15]  T. Jorgensen,et al.  Human HeLa cell enzymes that remove phosphoglycolate 3'-end groups from DNA. , 1992, Nucleic acids research.

[16]  P. Doetsch,et al.  Effects of abasic sites and DNA single-strand breaks on prokaryotic RNA polymerases. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[17]  P Bolton,et al.  A case-control family history study of autism. , 1994, Journal of child psychology and psychiatry, and allied disciplines.

[18]  G. Gascon,et al.  Ataxia-ocular motor apraxia syndrome: an investigation of cellular radiosensitivity of patients and their families. , 1994, Journal of medical genetics.

[19]  T. Jorgensen,et al.  Removal of 3'-phosphoglycolate from DNA strand-break damage in an oligonucleotide substrate by recombinant human apurinic/apyrimidinic endonuclease 1. , 1994, Nucleic acids research.

[20]  P. Doetsch,et al.  Transcription bypass or blockage at single-strand breaks on the DNA template strand: effect of different 3' and 5' flanking groups on the T7 RNA polymerase elongation complex. , 1994, Biochemistry.

[21]  J D Tucker,et al.  Characterization of the XRCC1-DNA ligase III complex in vitro and its absence from mutant hamster cells. , 1995, Nucleic acids research.

[22]  T. Lindahl,et al.  Post-translational modification of poly(ADP-ribose) polymerase induced by DNA strand breaks. , 1995, Trends in biochemical sciences.

[23]  Y. Matsumoto,et al.  Excision of deoxyribose phosphate residues by DNA polymerase beta during DNA repair. , 1995, Science.

[24]  A. Bailey,et al.  Autism as a strongly genetic disorder: evidence from a British twin study , 1995, Psychological Medicine.

[25]  A. Burgin,et al.  A eukaryotic enzyme that can disjoin dead-end covalent complexes between DNA and type I topoisomerases. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[26]  K. Caldecott,et al.  XRCC1 polypeptide interacts with DNA polymerase beta and possibly poly (ADP-ribose) polymerase, and DNA ligase III is a novel molecular 'nick-sensor' in vitro. , 1996, Nucleic acids research.

[27]  D. Lane,et al.  Two Pathways for Base Excision Repair in Mammalian Cells (*) , 1996, The Journal of Biological Chemistry.

[28]  Y. Pommier,et al.  Trapping of Mammalian Topoisomerase I and Recombinations Induced by Damaged DNA Containing Nicks or Gaps , 1997, The Journal of Biological Chemistry.

[29]  T. Lindahl,et al.  Second pathway for completion of human DNA base excision‐repair: reconstitution with purified proteins and requirement for DNase IV (FEN1) , 1997, The EMBO journal.

[30]  Ping Fang,et al.  De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome , 1997, Nature Genetics.

[31]  K. Kohn,et al.  Effects of Uracil Incorporation, DNA Mismatches, and Abasic Sites on Cleavage and Religation Activities of Mammalian Topoisomerase I* , 1997, The Journal of Biological Chemistry.

[32]  B. Leventhal,et al.  Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. , 1997, American journal of human genetics.

[33]  K. Caldecott,et al.  Role of the DNA ligase III zinc finger in polynucleotide binding and ligation. , 1998, Nucleic acids research.

[34]  J. Piven,et al.  Autism and Tuberous Sclerosis Complex: Prevalence and Clinical Features , 1998, Journal of autism and developmental disorders.

[35]  Deborah D. Hatton,et al.  Autistic Behavior in Young Boys with Fragile X Syndrome , 1998, Journal of autism and developmental disorders.

[36]  A. Bailey,et al.  A clinicopathological study of autism. , 1998, Brain : a journal of neurology.

[37]  Stephen J. Guter,et al.  Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. , 1998, American journal of human genetics.

[38]  T. Tullius,et al.  Oxidative Strand Scission of Nucleic Acids: Routes Initiated by Hydrogen Abstraction from the Sugar Moiety. , 1998, Chemical reviews.

[39]  C. Francks,et al.  A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium. , 1998, Human molecular genetics.

[40]  J. Ménissier-de murcia,et al.  DNA repair defect in poly(ADP-ribose) polymerase-deficient cell lines. , 1998, Nucleic acids research.

[41]  S. Scherer,et al.  Molecular Cloning of the Human Gene, PNKP, Encoding a Polynucleotide Kinase 3′-Phosphatase and Evidence for Its Role in Repair of DNA Strand Breaks Caused by Oxidative Damage* , 1999, The Journal of Biological Chemistry.

[42]  Peter Shrager,et al.  Caspr2, a New Member of the Neurexin Superfamily, Is Localized at the Juxtaparanodes of Myelinated Axons and Associates with K+ Channels , 1999, Neuron.

[43]  H. Zoghbi,et al.  Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.

[44]  M. Otterlei,et al.  Post‐replicative base excision repair in replication foci , 1999, The EMBO journal.

[45]  Y. Pommier,et al.  Induction of Reversible Complexes between Eukaryotic DNA Topoisomerase I and DNA-containing Oxidative Base Damages , 1999, The Journal of Biological Chemistry.

[46]  A. Tomkinson,et al.  DNA Ligase III Is Recruited to DNA Strand Breaks by a Zinc Finger Motif Homologous to That of Poly(ADP-ribose) Polymerase , 1999, The Journal of Biological Chemistry.

[47]  J. Sgouros,et al.  Molecular Characterization of a Human DNA Kinase* , 1999, The Journal of Biological Chemistry.

[48]  B. J. Williams,et al.  Autism and Autistic Behavior in Joubert Syndrome , 1999, Journal of child neurology.

[49]  J. Pouliot,et al.  Yeast gene for a Tyr-DNA phosphodiesterase that repairs topoisomerase I complexes. , 1999, Science.

[50]  G. Poirier,et al.  Poly(ADP-ribosyl)ation reactions in the regulation of nuclear functions. , 1999, The Biochemical journal.

[51]  J. Pleschke,et al.  Poly(ADP-ribose) Binds to Specific Domains in DNA Damage Checkpoint Proteins* , 2000, The Journal of Biological Chemistry.

[52]  Samuel H. Wilson,et al.  FEN1 Stimulation of DNA Polymerase β Mediates an Excision Step in Mammalian Long Patch Base Excision Repair* , 2000, The Journal of Biological Chemistry.

[53]  K. Caldecott,et al.  The DNA ligase III zinc finger stimulates binding to DNA secondary structure and promotes end joining. , 2000, Nucleic acids research.

[54]  A. Tomkinson,et al.  Requirement for human AP endonuclease 1 for repair of 3'-blocking damage at DNA single-strand breaks induced by reactive oxygen species. , 2000, Carcinogenesis.

[55]  V. Schreiber,et al.  Base excision repair is impaired in mammalian cells lacking Poly(ADP-ribose) polymerase-1. , 2000, Biochemistry.

[56]  Penny A. Johnson,et al.  A Cell Cycle-Specific Requirement for the XRCC1 BRCT II Domain during Mammalian DNA Strand Break Repair , 2000, Molecular and Cellular Biology.

[57]  J. Weber,et al.  Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[58]  E. Dogliotti,et al.  DNA polymerase beta is required for efficient DNA strand break repair induced by methyl methanesulfonate but not by hydrogen peroxide. , 2000, Nucleic acids research.

[59]  K. Caldecott,et al.  Mutation of a BRCT domain selectively disrupts DNA single-strand break repair in noncycling Chinese hamster ovary cells. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[60]  K. Caldecott Mammalian DNA single‐strand break repair: an X‐ra(y)ted affair , 2001, BioEssays : news and reviews in molecular, cellular and developmental biology.

[61]  Samuel H. Wilson,et al.  DNA Polymerase (cid:1) -mediated Long Patch Base Excision Repair POLY(ADP-RIBOSE) POLYMERASE-1 STIMULATES STRAND DISPLACEMENT DNA SYNTHESIS* , 2022 .

[62]  M. Weinfeld,et al.  XRCC1 Stimulates Human Polynucleotide Kinase Activity at Damaged DNA Termini and Accelerates DNA Single-Strand Break Repair , 2001, Cell.

[63]  J. Darnell,et al.  Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome , 2001, Cell.

[64]  M. Koenig,et al.  Homozygosity mapping of Portuguese and Japanese forms of ataxia-oculomotor apraxia to 9p13, and evidence for genetic heterogeneity. , 2001, American journal of human genetics.

[65]  K. C. Nitiss,et al.  Overexpression of Type I Topoisomerases Sensitizes Yeast Cells to DNA Damage* , 2001, The Journal of Biological Chemistry.

[66]  D. Wilkin,et al.  Neuron , 2001, Brain Research.

[67]  Stephen J. Guter,et al.  A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. , 2001, American journal of human genetics.

[68]  T. Kunkel,et al.  Identification of an Intrinsic 5′-Deoxyribose-5-phosphate Lyase Activity in Human DNA Polymerase λ , 2001, The Journal of Biological Chemistry.

[69]  K. Davis,et al.  Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. , 2001, American journal of human genetics.

[70]  L. Davidovic,et al.  Importance of poly(ADP-ribose) glycohydrolase in the control of poly(ADP-ribose) metabolism. , 2001, Experimental cell research.

[71]  T. Wassink,et al.  Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder , 2001, Molecular Psychiatry.

[72]  Axel Benner,et al.  Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. , 2001, Human molecular genetics.

[73]  U. Lakshmipathy,et al.  Antisense-mediated decrease in DNA ligase III expression results in reduced mitochondrial DNA integrity. , 2001, Nucleic acids research.

[74]  Y. Pommier,et al.  Topoisomerase I-mediated DNA damage. , 2001, Advances in cancer research.

[75]  A. Kuzminov Single-strand interruptions in replicating chromosomes cause double-strand breaks , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[76]  P. Coutinho,et al.  Recessive ataxia with ocular apraxia: review of 22 Portuguese patients. , 2001, Archives of neurology.

[77]  R. Borgatti,et al.  Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome. , 2001, American journal of human genetics.

[78]  D. Geschwind,et al.  A genomewide screen for autism susceptibility loci. , 2001, American journal of human genetics.

[79]  J. Clayton-Smith,et al.  Angelman syndrome phenotype associated with mutations inMECP2, a gene encoding a methyl CpG binding protein , 2001, Journal of medical genetics.

[80]  J. Pevsner,et al.  Postmortem brain abnormalities of the glutamate neurotransmitter system in autism , 2001, Neurology.

[81]  Samuel H. Wilson,et al.  5'-Deoxyribose Phosphate Lyase Activity of Human DNA Polymerase ɩ in Vitro , 2001, Science.

[82]  S. Spence,et al.  The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions. , 2001, American journal of human genetics.

[83]  L. Freund,et al.  Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome. , 2001, American journal of medical genetics.

[84]  L. Povirk,et al.  Conversion of Phosphoglycolate to Phosphate Termini on 3′ Overhangs of DNA Double Strand Breaks by the Human Tyrosyl-DNA Phosphodiesterase hTdp1* , 2002, The Journal of Biological Chemistry.

[85]  J. Gilbert,et al.  Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. , 2001, American journal of human genetics.

[86]  JAMES C. Wang,et al.  Cellular roles of DNA topoisomerases: a molecular perspective , 2002, Nature Reviews Molecular Cell Biology.

[87]  J. Buxbaum,et al.  Association between a GABRB3 polymorphism and autism , 2002, Molecular Psychiatry.

[88]  M. DeMott,et al.  Dynamics and diversions in base excision DNA repair of oxidized abasic lesions , 2002, Oncogene.

[89]  D. Geschwind,et al.  Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. , 2002, American journal of human genetics.

[90]  P. Dollé,et al.  Poly(ADP-ribose) Polymerase-2 (PARP-2) Is Required for Efficient Base Excision DNA Repair in Association with PARP-1 and XRCC1* , 2002, The Journal of Biological Chemistry.

[91]  L. Peltonen,et al.  A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. , 2002, American journal of human genetics.

[92]  E. Gershon,et al.  Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7 , 2002, Molecular Psychiatry.

[93]  A. Spradling,et al.  The Drosophila heterochromatic gene encoding poly(ADP-ribose) polymerase (PARP) is required to modulate chromatin structure during development. , 2002, Genes & development.

[94]  B. Houston Encyclopedia of Genetics , 2002 .

[95]  Stephen J. Guter,et al.  Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder , 2002, Molecular Psychiatry.

[96]  A. Barzilai,et al.  ATM deficiency and oxidative stress: a new dimension of defective response to DNA damage. , 2002, DNA repair.

[97]  Lon R. Cardon,et al.  Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia , 2002, Nature Genetics.

[98]  P. O'Connell,et al.  Linkage of high-density lipoprotein–cholesterol concentrations to a locus on chromosome 9p in Mexican Americans , 2002, Nature Genetics.

[99]  T. Bourgeron,et al.  Linkage and association of the glutamate receptor 6 gene with autism , 2002, Molecular Psychiatry.

[100]  M. Hottiger,et al.  Acetylation regulates the DNA end-trimming activity of DNA polymerase beta. , 2002, Molecular cell.

[101]  T. Lindahl,et al.  Down-regulation of DNA repair synthesis at DNA single-strand interruptions in poly(ADP-ribose) polymerase-1 deficient murine cell extracts. , 2002, DNA repair.

[102]  J. Lupski,et al.  Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy , 2002, Nature Genetics.

[103]  Yves Pommier,et al.  Association of XRCC1 and tyrosyl DNA phosphodiesterase (Tdp1) for the repair of topoisomerase I-mediated DNA lesions. , 2003, DNA repair.

[104]  V. Schreiber,et al.  Poly(ADP-ribose) Polymerase-1 (PARP-1) Is Required in Murine Cell Lines for Base Excision Repair of Oxidative DNA Damage in the Absence of DNA Polymerase β* , 2003, The Journal of Biological Chemistry.

[105]  Ruth A. Carper,et al.  Evidence of brain overgrowth in the first year of life in autism. , 2003, JAMA.

[106]  K. Caldecott DNA Single-Strand Break Repair and Spinocerebellar Ataxia , 2003, Cell.

[107]  M. Tomicic,et al.  APE/Ref-1 and the mammalian response to genotoxic stress. , 2003, Toxicology.

[108]  H. Zoghbi Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? , 2003, Science.

[109]  Thomas Bourgeron,et al.  Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism , 2003, Nature Genetics.

[110]  S. Rivaud-Pechoux,et al.  Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies. , 2003, Brain : a journal of neurology.

[111]  J. Constantino,et al.  Autistic traits in the general population: a twin study. , 2003, Archives of general psychiatry.

[112]  A. Yasui,et al.  Spatial and Temporal Cellular Responses to Single-Strand Breaks in Human Cells , 2003, Molecular and Cellular Biology.

[113]  Mitsuko Masutani,et al.  A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage. , 2003, Nucleic acids research.

[114]  P. Mundy Annotation: the neural basis of social impairments in autism: the role of the dorsal medial-frontal cortex and anterior cingulate system. , 2003, Journal of child psychology and psychiatry, and allied disciplines.

[115]  S. Klauck,et al.  Analysis of reelin as a candidate gene for autism , 2003, Molecular Psychiatry.

[116]  A. Spradling,et al.  Chromatin Loosening by Poly(ADP)-Ribose Polymerase (PARP) at Drosophila Puff Loci , 2003, Science.

[117]  E. Petermann,et al.  ATP-dependent selection between single nucleotide and long patch base excision repair. , 2003, DNA repair.

[118]  S. Spence,et al.  A genomewide screen of 345 families for autism-susceptibility loci. , 2003, American journal of human genetics.

[119]  Samuel H. Wilson,et al.  Base Excision Repair Intermediates Induce p53-independent Cytotoxic and Genotoxic Responses* , 2003, Journal of Biological Chemistry.

[120]  K. Caldecott XRCC1 and DNA strand break repair. , 2003, DNA repair.

[121]  K. Tyler,et al.  Recurrent dermatomal vesicular skin lesions: a clue to diagnosis of herpes simplex virus 2 meningitis. , 2003, Archives of neurology.

[122]  W. Salinger,et al.  Behavioral phenotype of the reeler mutant mouse: effects of RELN gene dosage and social isolation. , 2003, Behavioral neuroscience.

[123]  H. McDermid,et al.  Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms , 2003, Journal of medical genetics.

[124]  A. Beaudet,et al.  Autism in Angelman syndrome: implications for autism research , 2004, Clinical genetics.

[125]  Leroy F. Liu,et al.  Hydrogen Peroxide Induces Topoisomerase I-mediated DNA Damage and Cell Death* , 2004, Journal of Biological Chemistry.

[126]  S. Tsuji,et al.  The FHA domain of aprataxin interacts with the C-terminal region of XRCC1. , 2004, Biochemical and biophysical research communications.

[127]  T. Gilliam,et al.  Molecular triangulation: bridging linkage and molecular-network information for identifying candidate genes in Alzheimer's disease. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[128]  Kenny Q. Ye,et al.  Large-Scale Copy Number Polymorphism in the Human Genome , 2004, Science.

[129]  R. Benayed,et al.  Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder , 2004, Molecular Psychiatry.

[130]  D. Chugani Serotonin in autism and pediatric epilepsies. , 2004, Mental retardation and developmental disabilities research reviews.

[131]  J. Hallmayer,et al.  Perinatal factors and the development of autism: a population study. , 2004, Archives of general psychiatry.

[132]  B. Chen,et al.  A New XRCC1-Containing Complex and Its Role in Cellular Survival of Methyl Methanesulfonate Treatment , 2004, Molecular and Cellular Biology.

[133]  D. Durocher,et al.  Xrcc4 physically links DNA end processing by polynucleotide kinase to DNA ligation by DNA ligase IV , 2004, The EMBO journal.

[134]  J. Hallmayer,et al.  Using self-report to identify the broad phenotype in parents of children with autistic spectrum disorders: a study using the Autism-Spectrum Quotient. , 2004, Journal of child psychology and psychiatry, and allied disciplines.

[135]  Scott D. Kathe,et al.  Single-Stranded Breaks in DNA but Not Oxidative DNA Base Damages Block Transcriptional Elongation by RNA Polymerase II in HeLa Cell Nuclear Extracts* , 2004, Journal of Biological Chemistry.

[136]  S. Priori,et al.  CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism , 2004, Cell.

[137]  G. Dianov,et al.  APE1 is the major 3'-phosphoglycolate activity in human cell extracts. , 2004, Nucleic acids research.

[138]  Osamu Onodera,et al.  Aprataxin, a novel protein that protects against genotoxic stress. , 2004, Human molecular genetics.

[139]  S. Schwartz,et al.  Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum. , 2004, Pediatrics.

[140]  L. Peltonen,et al.  Genome-wide scan for loci of Asperger syndrome , 2004, Molecular Psychiatry.

[141]  Dai Zhang,et al.  Family‐based association study between autism and glutamate receptor 6 gene in Chinese Han trios , 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[142]  J. Buxbaum,et al.  Linkage analysis for autism in a subset families with obsessive–compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19 , 2004, Molecular Psychiatry.

[143]  K. Davis,et al.  Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism. , 2004, The American journal of psychiatry.

[144]  C. Walsh,et al.  Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome , 2004, Nature Genetics.

[145]  J. Bressler,et al.  A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A , 2004, American journal of medical genetics. Part A.

[146]  P. Calsou,et al.  Involvement of Poly(ADP-ribose) Polymerase-1 and XRCC1/DNA Ligase III in an Alternative Route for DNA Double-strand Breaks Rejoining* , 2004, Journal of Biological Chemistry.

[147]  K. Caldecott DNA single-strand breaks and neurodegeneration. , 2004, DNA repair.

[148]  Albert David,et al.  X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. , 2004, American journal of human genetics.

[149]  D. Chan,et al.  The Protein Kinase CK2 Facilitates Repair of Chromosomal DNA Single-Strand Breaks , 2004, Cell.

[150]  Igor Tsigelny,et al.  The Arg451Cys-Neuroligin-3 Mutation Associated with Autism Reveals a Defect in Protein Processing , 2004, The Journal of Neuroscience.

[151]  S. Tsuji,et al.  Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein , 2004, Annals of neurology.

[152]  P. Mosesso,et al.  The novel human gene aprataxin is directly involved in DNA single-strand-break repair , 2005, Cellular and Molecular Life Sciences CMLS.

[153]  K. Davis,et al.  Linkage and Association of the Mitochondrial Aspartate / Glutamate Carrier SLC 25 A 12 Gene With Autism , 2004 .

[154]  C. Brenner,et al.  The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4. , 2004, DNA repair.

[155]  D. Geschwind,et al.  Evidence for sex-specific risk alleles in autism spectrum disorder. , 2004, American journal of human genetics.

[156]  Stephanie Hayes,et al.  The factor structure of autistic traits. , 2004, Journal of child psychology and psychiatry, and allied disciplines.

[157]  Jinshui Fan,et al.  XRCC1 co-localizes and physically interacts with PCNA. , 2004, Nucleic acids research.

[158]  Samuel H. Wilson,et al.  In situ analysis of repair processes for oxidative DNA damage in mammalian cells. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[159]  G. de Murcia,et al.  The PARP superfamily , 2004, BioEssays : news and reviews in molecular, cellular and developmental biology.

[160]  Nils Brose,et al.  The complexity of PDZ domain-mediated interactions at glutamatergic synapses: a case study on neuroligin , 2004, Neuropharmacology.

[161]  Samuel H. Wilson,et al.  AP endonuclease-independent DNA base excision repair in human cells. , 2004, Molecular cell.

[162]  Mark F Bear,et al.  The mGluR theory of fragile X mental retardation , 2004, Trends in Neurosciences.

[163]  W. Kress,et al.  Aprataxin mutations are a rare cause of early onset ataxia in Germany , 2004, Journal of Neurology.

[164]  H. Wong,et al.  DNA damage levels and biochemical repair capacities associated with XRCC1 deficiency. , 2005, Biochemistry.

[165]  Eric Fombonne,et al.  Epidemiology of autistic disorder and other pervasive developmental disorders. , 2005, The Journal of clinical psychiatry.

[166]  Jing Liu,et al.  Positive Association of the Oxytocin Receptor Gene (OXTR) with Autism in the Chinese Han Population , 2005, Biological Psychiatry.

[167]  J. Piven,et al.  Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene , 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[168]  D. Geschwind,et al.  Replication of autism linkage: fine-mapping peak at 17q21. , 2005, American journal of human genetics.

[169]  W. McMahon,et al.  Evidence for Linkage on Chromosome 3q25–27 in a Large Autism Extended Pedigree , 2006, Human Heredity.

[170]  M. Y. Kim,et al.  Poly(ADP-ribosyl)ation by PARP-1: 'PAR-laying' NAD+ into a nuclear signal. , 2005, Genes & development.

[171]  G. Dianov,et al.  Poly(ADP‐ribose) polymerase‐1 protects excessive DNA strand breaks from deterioration during repair in human cell extracts , 2005, The FEBS journal.

[172]  M. Gill,et al.  Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31. , 2005, The American journal of psychiatry.

[173]  C. Brenner,et al.  Disease-associated Mutations Inactivate AMP-Lysine Hydrolase Activity of Aprataxin*♦ , 2005, Journal of Biological Chemistry.

[174]  T. Südhof,et al.  A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins. , 2005, Neuron.

[175]  G. Dawson,et al.  Autism and the serotonin transporter: the long and short of it , 2005, Molecular Psychiatry.

[176]  J. Sutcliffe,et al.  Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors. , 2005, American journal of human genetics.

[177]  J. Lupski,et al.  Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1 , 2005, Nature.

[178]  Emanuel Dicicco-Bloom,et al.  Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. , 2005, American journal of human genetics.

[179]  Samuel H. Wilson,et al.  DNA Polymerase (cid:1) Protects Mouse Fibroblasts against Oxidative DNA Damage and Is Recruited to Sites of DNA Damage/Repair* , 2005 .

[180]  C Eng,et al.  Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations , 2005, Journal of Medical Genetics.

[181]  J. Champoux,et al.  Human Tdp1 Cleaves a Broad Spectrum of Substrates, Including Phosphoamide Linkages* , 2005, Journal of Biological Chemistry.

[182]  J. Champoux,et al.  SCAN1 mutant Tdp1 accumulates the enzyme–DNA intermediate and causes camptothecin hypersensitivity , 2005, The EMBO journal.

[183]  Thomas C. Südhof,et al.  A Splice Code for trans-Synaptic Cell Adhesion Mediated by Binding of Neuroligin 1 to α- and β-Neurexins , 2005, Neuron.

[184]  Rodney C Samaco,et al.  Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. , 2005, Human molecular genetics.

[185]  M. Keddache,et al.  Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression , 2005, Molecular Psychiatry.

[186]  A. Zimmerman,et al.  Neuroglial activation and neuroinflammation in the brain of patients with autism , 2005, Annals of neurology.

[187]  N. Craddock,et al.  Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients , 2005, Molecular Psychiatry.

[188]  Huichen Wang,et al.  DNA ligase III as a candidate component of backup pathways of nonhomologous end joining. , 2005, Cancer research.

[189]  E Maestrini,et al.  Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects , 2005, Journal of Medical Genetics.

[190]  D. Geschwind,et al.  Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs , 2005, Molecular Psychiatry.

[191]  C. Mathew Encyclopedia of genetics, genomics, proteomics and bioinformatics. , 2005 .

[192]  J. Lupski,et al.  Deficiency in 3′-phosphoglycolate processing in human cells with a hereditary mutation in tyrosyl-DNA phosphodiesterase (TDP1) , 2005, Nucleic acids research.

[193]  M. Crescenzi,et al.  The accumulation of MMS-induced single strand breaks in G1 phase is recombinogenic in DNA polymerase β defective mammalian cells , 2005, Nucleic acids research.

[194]  G. De Michele,et al.  Very late onset in ataxia oculomotor apraxia type I , 2005, Annals of neurology.

[195]  F. Daboussi,et al.  APE1 overexpression in XRCC1-deficient cells complements the defective repair of oxidative single strand breaks but increases genomic instability , 2005, Nucleic acids research.

[196]  V S Caviness,et al.  Brain asymmetries in autism and developmental language disorder: a nested whole-brain analysis. , 2004, Brain : a journal of neurology.

[197]  J. Sutcliffe,et al.  Analysis of the RELN gene as a genetic risk factor for autism , 2005, Molecular Psychiatry.

[198]  Rebecca C. Knickmeyer,et al.  Topical Review: Fetal Testosterone and Sex Differences in Typical Social Development and in Autism , 2006, Journal of child neurology.

[199]  D. Geschwind,et al.  Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families , 2006, Annals of neurology.

[200]  R. Costa,et al.  Chk2 Mediates Stabilization of the FoxM1 Transcription Factor To Stimulate Expression of DNA Repair Genes , 2006, Molecular and Cellular Biology.

[201]  P. Bolton,et al.  Genetic heterogeneity between the three components of the autism spectrum: a twin study. , 2006, Journal of the American Academy of Child and Adolescent Psychiatry.

[202]  H. Leonhardt,et al.  Differential recruitment of DNA Ligase I and III to DNA repair sites , 2006, Nucleic Acids Research.

[203]  M. Butler,et al.  Expression of 4 Genes Between Chromosome 15 Breakpoints 1 and 2 and Behavioral Outcomes in Prader-Willi Syndrome , 2006, Pediatrics.

[204]  M. Bjornsti,et al.  Trapping of DNA topoisomerase I on nick-containing DNA in cell free extracts of Saccharomyces cerevisiae. , 2006, DNA repair.

[205]  D. Geschwind,et al.  Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder , 2006, Molecular Psychiatry.

[206]  Deborah D. Hatton,et al.  Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP , 2006, American journal of medical genetics. Part A.

[207]  Jennifer H. Pfeifer,et al.  Understanding emotions in others: mirror neuron dysfunction in children with autism spectrum disorders , 2006, Nature Neuroscience.

[208]  N. Gueven,et al.  Nucleolar localization of aprataxin is dependent on interaction with nucleolin and on active ribosomal DNA transcription. , 2006, Human molecular genetics.

[209]  S. White,et al.  Tyrosyl-DNA phosphodiesterase (Tdp1) participates in the repair of Top2-mediated DNA damage. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[210]  Astrid M. Vicente,et al.  Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels , 2007, Human Genetics.

[211]  A. Kuzminov,et al.  Fragmentation of replicating chromosomes triggered by uracil in DNA. , 2006, Journal of molecular biology.

[212]  H. Engeland,et al.  Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism , 2006, Molecular Psychiatry.

[213]  Jung-Suk Sung,et al.  Roles of base excision repair subpathways in correcting oxidized abasic sites in DNA , 2006, The FEBS journal.

[214]  D. Stephan,et al.  Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. , 2006, The New England journal of medicine.

[215]  Bryan Frank,et al.  Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes , 2006, BMC Genomics.

[216]  L. Peltonen,et al.  A heterogeneity-based genome search meta-analysis for autism-spectrum disorders , 2006, Molecular Psychiatry.

[217]  F. Serajee,et al.  Association of Reelin gene polymorphisms with autism. , 2006, Genomics.

[218]  Pat Levitt,et al.  A genetic variant that disrupts MET transcription is associated with autism , 2006, Proceedings of the National Academy of Sciences.

[219]  S. West,et al.  The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates , 2006, Nature.

[220]  R Redon,et al.  Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders , 2006, Journal of Medical Genetics.

[221]  K. Caldecott,et al.  TDP1-dependent DNA single-strand break repair and neurodegeneration. , 2006, Mutagenesis.

[222]  J. Gregg,et al.  Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes. , 2006, Human molecular genetics.

[223]  Richard E Thompson,et al.  Abnormalities of cholesterol metabolism in autism spectrum disorders , 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[224]  Charles E. Schwartz,et al.  High frequency of neurexin 1β signal peptide structural variants in patients with autism , 2006, Neuroscience Letters.

[225]  R. Ebstein,et al.  Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skills , 2006, Molecular Psychiatry.

[226]  J. Harris,et al.  Aprataxin Forms a Discrete Branch in the HIT (Histidine Triad) Superfamily of Proteins with Both DNA/RNA Binding and Nucleotide Hydrolase Activities* , 2006, Journal of Biological Chemistry.

[227]  J. Sutcliffe,et al.  Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility , 2006, European Journal of Human Genetics.

[228]  Mark Weiser,et al.  Advancing paternal age and autism. , 2006, Archives of general psychiatry.

[229]  Bassem A. Hassan,et al.  Gene prioritization through genomic data fusion , 2006, Nature Biotechnology.

[230]  G. Dawson,et al.  Evidence for multiple loci from a genome scan of autism kindreds , 2006, Molecular Psychiatry.

[231]  D. Geschwind,et al.  Genome-wide analyses of human perisylvian cerebral cortical patterning , 2007, Proceedings of the National Academy of Sciences.

[232]  Y. Itoyama,et al.  DNA single‐strand break repair is impaired in aprataxin‐related ataxia , 2007, Annals of neurology.

[233]  D. Geschwind,et al.  Autism spectrum disorders: developmental disconnection syndromes , 2007, Current Opinion in Neurobiology.

[234]  D. Stephan,et al.  A survey of genetic human cortical gene expression , 2007, Nature Genetics.

[235]  Pat Levitt,et al.  Disruption of cerebral cortex MET signaling in autism spectrum disorder , 2007, Annals of neurology.

[236]  G. Maga,et al.  Human base excision repair complex is physically associated to DNA replication and cell cycle regulatory proteins , 2007, Nucleic acids research.

[237]  J. Gilbert,et al.  Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14 , 2007, Molecular Psychiatry.

[238]  Stephen T Warren,et al.  Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. , 2007, Human molecular genetics.

[239]  Zhao-Qi Wang,et al.  Altered poly(ADP-ribose) metabolism impairs cellular responses to genotoxic stress in a hypomorphic mutant of poly(ADP-ribose) glycohydrolase. , 2007, Experimental cell research.

[240]  K. Caldecott,et al.  Poly(ADP-Ribose) Polymerase 1 Accelerates Single-Strand Break Repair in Concert with Poly(ADP-Ribose) Glycohydrolase , 2007, Molecular and Cellular Biology.

[241]  Mark F. Bear,et al.  Correction of Fragile X Syndrome in Mice , 2007, Neuron.

[242]  Thomas Bourgeron,et al.  Mapping autism risk loci using genetic linkage and chromosomal rearrangements , 2007, Nature Genetics.

[243]  Simon Heath,et al.  A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 , 2007, Nature Genetics.

[244]  Thomas Bourgeron,et al.  Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders , 2007, Nature Genetics.

[245]  Kenny Q. Ye,et al.  Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.

[246]  K. Caldecott Mammalian single-strand break repair: mechanisms and links with chromatin. , 2007, DNA repair.

[247]  Mira Park,et al.  Family-based association study between GRIK2 polymorphisms and autism spectrum disorders in the Korean trios , 2007, Neuroscience Research.

[248]  C. Freitag,et al.  The genetics of autistic disorders and its clinical relevance: a review of the literature , 2007, Molecular Psychiatry.

[249]  Y. Furiya,et al.  Short half-lives of ataxia-associated aprataxin proteins in neuronal cells , 2007, Neuroscience Letters.

[250]  Kenny Q. Ye,et al.  A unified genetic theory for sporadic and inherited autism , 2007, Proceedings of the National Academy of Sciences.

[251]  Christian R Marshall,et al.  Contribution of SHANK3 mutations to autism spectrum disorder. , 2007, American journal of human genetics.

[252]  Jacqueline Blundell,et al.  A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice , 2007, Science.

[253]  A. Durr,et al.  Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1 , 2007, Neurology.

[254]  A. Begg,et al.  Role for DNA polymerase beta in response to ionizing radiation. , 2007, DNA repair.

[255]  P. Hergenrother,et al.  Poly(ADP-ribose) makes a date with death. , 2007, Current opinion in chemical biology.

[256]  N. Mailand,et al.  Human Xip1 (C2orf13) Is a Novel Regulator of Cellular Responses to DNA Strand Breaks* , 2007, Journal of Biological Chemistry.

[257]  C. Cass,et al.  XRCC1 Stimulates Polynucleotide Kinase by Enhancing Its Damage Discrimination and Displacement from DNA Repair Intermediates* , 2007, Journal of Biological Chemistry.

[258]  S. West,et al.  Actions of Aprataxin in Multiple DNA Repair Pathways* , 2007, Journal of Biological Chemistry.

[259]  M. Butler,et al.  Whole genome microarray analysis of gene expression in subjects with fragile X syndrome , 2007, Genetics in Medicine.

[260]  Teiichi Furuichi,et al.  Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients. , 2007, The Journal of clinical investigation.

[261]  Joseph Piven,et al.  Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism. , 2007, Archives of general psychiatry.

[262]  R. Dolmetsch,et al.  Molecular mechanisms of autism: a possible role for Ca2+ signaling , 2007, Current Opinion in Neurobiology.

[263]  M. Farrer,et al.  Aprataxin (APTX) gene mutations resembling multiple system atrophy. , 2007, Parkinsonism & related disorders.

[264]  D. Geschwind,et al.  High density SNP association study of a major autism linkage region on chromosome 17. , 2007, Human molecular genetics.

[265]  Christa Lese Martin,et al.  Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism , 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[266]  K. Caldecott,et al.  APLF (C2orf13) Is a Novel Human Protein Involved in the Cellular Response to Chromosomal DNA Strand Breaks , 2007, Molecular and Cellular Biology.

[267]  S. West,et al.  Defective DNA Repair and Neurodegenerative Disease , 2007, Cell.

[268]  Sufang Yang,et al.  Ischemic preconditioning induces XRCC1, DNA polymerase-beta, and DNA ligase III and correlates with enhanced base excision repair. , 2007, DNA repair.

[269]  J. LaSalle,et al.  15 q 11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders , 2007 .

[270]  K. Caldecott,et al.  TDP1 facilitates repair of ionizing radiation-induced DNA single-strand breaks. , 2007, DNA repair.

[271]  A. Lu,et al.  A quantitative trait locus analysis of social responsiveness in multiplex autism families. , 2007, The American journal of psychiatry.

[272]  D. Pinto,et al.  Contribution of SHANK 3 Mutations to Autism Spectrum Disorder , 2007 .

[273]  S. Nakajima,et al.  A novel human AP endonuclease with conserved zinc‐finger‐like motifs involved in DNA strand break responses , 2007, The EMBO journal.

[274]  Z. Tümer,et al.  Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome , 2007, European Journal of Human Genetics.

[275]  G. Dianov,et al.  Co-ordination of DNA single strand break repair. , 2007, DNA repair.

[276]  K. Caldecott,et al.  TDP1 facilitates chromosomal single‐strand break repair in neurons and is neuroprotective in vivo , 2007, The EMBO journal.

[277]  P. Degan,et al.  Terminally differentiated muscle cells are defective in base excision DNA repair and hypersensitive to oxygen injury , 2007, Proceedings of the National Academy of Sciences.

[278]  D. Geschwind,et al.  LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia , 2007, Molecular Psychiatry.

[279]  Ananya De,et al.  A novel interaction between DNA ligase III and DNA polymerase gamma plays an essential role in mitochondrial DNA stability. , 2007, The Biochemical journal.

[280]  Lorraine Potocki,et al.  Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype. , 2007, American journal of human genetics.

[281]  Kimiyoshi Arimura,et al.  Spinocerebellar ataxia with axonal neuropathy. , 2010, Advances in experimental medicine and biology.

[282]  C. Verweij,et al.  Heritability of autistic traits in the general population. , 2007, Archives of pediatrics & adolescent medicine.

[283]  A. Yasui,et al.  Recruitment of DNA repair synthesis machinery to sites of DNA damage/repair in living human cells , 2007, Nucleic acids research.

[284]  J. LaSalle,et al.  15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. , 2007, Human molecular genetics.

[285]  Joshua M. Korn,et al.  Association between microdeletion and microduplication at 16p11.2 and autism. , 2008, The New England journal of medicine.

[286]  G. Dianov,et al.  CHIP-mediated degradation and DNA damage-dependent stabilization regulate base excision repair proteins. , 2008, Molecular cell.

[287]  Eric Hollander,et al.  Autism‐related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism , 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[288]  F. Moroni Poly(ADP-ribose)polymerase 1 (PARP-1) and postischemic brain damage. , 2008, Current opinion in pharmacology.

[289]  Timothy M. DeLorey,et al.  Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: A potential model of autism spectrum disorder , 2008, Behavioural Brain Research.

[290]  Geraldine Dawson,et al.  Heterogeneous association between engrailed‐2 and autism in the CPEA network , 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[291]  J. Gregg,et al.  Gene expression changes in children with autism. , 2008, Genomics.

[292]  T Varilo,et al.  Association of DISC1 with autism and Asperger syndrome , 2008, Molecular Psychiatry.

[293]  Jing Liu,et al.  Association of the ENGRAILED 2 (EN2) gene with autism in Chinese Han population , 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[294]  D. Pinto,et al.  Structural variation of chromosomes in autism spectrum disorder. , 2008, American journal of human genetics.

[295]  Katarzyna Chawarska,et al.  Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. , 2008, American journal of human genetics.

[296]  Y. Uchiyama,et al.  Characterization of plant XRCC1 and its interaction with proliferating cell nuclear antigen , 2008, Planta.

[297]  C. Lopez,et al.  E2F1 Regulates the Base Excision Repair Gene XRCC1 and Promotes DNA Repair* , 2008, Journal of Biological Chemistry.

[298]  J. Shao,et al.  The association analysis of RELN and GRM8 genes with autistic spectrum disorder in chinese han population , 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[299]  R. Ebstein,et al.  Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition , 2008, Molecular Psychiatry.

[300]  D. Conrad,et al.  Recurrent 16p11.2 microdeletions in autism. , 2007, Human molecular genetics.

[301]  Joseph Piven,et al.  Defining key features of the broad autism phenotype: A comparison across parents of multiple‐ and single‐incidence autism families , 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[302]  J. Sebat,et al.  Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. , 2008, American journal of human genetics.

[303]  Tanya M. Teslovich,et al.  A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. , 2008, American journal of human genetics.

[304]  S. Mitra,et al.  Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells , 2008, Cell Research.

[305]  A. Tomkinson,et al.  Two DNA-binding and Nick Recognition Modules in Human DNA Ligase III* , 2008, Journal of Biological Chemistry.