Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence
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Doron Lancet | Alessandro Orro | Luciano Milanesi | Erika Salvi | Fabio Macciardi | Matteo Fumagalli | Gabriele Trombetti | Paolo Cozzi | Bernard Lerer | Manuela Sironi | Sara Lupoli | J. Beckmann | L. Milanesi | D. Lancet | K. Kanyas | B. Lerer | F. Macciardi | M. Fumagalli | Federica Torri | E. Salvi | S. Lupoli | R. Cagliani | M. Sironi | E. Ben‐Asher | D. Amann-Zalcenstein | A. Orro | P. Cozzi | Yoav Kohn | Rachele Cagliani | Jacques S. Beckmann | Kyra Kanyas | Federica Torri | Anna Akelai | Daniela Amann‐Zalcenstein | Chiara Dal Fiume | Edna Ben‐Asher | Luisa Strik Lievers | Richard B. Ebstein | Y. Kohn | G. Trombetti | Richard B. Ebstein | L. S. Lievers | C. D. Fiume | Anna Akelai
[1] E. Gershon,et al. Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia , 2002, Molecular Psychiatry.
[2] J. Os,et al. Aetiological heterogeneity and course of illness in the functional psychoses: A prospective follow-up study , 1993, Schizophrenia Research.
[3] J. Beckmann,et al. Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval , 2005, European Journal of Human Genetics.
[4] Kyle Summers,et al. Adaptive evolution of genes underlying schizophrenia , 2007, Proceedings of the Royal Society B: Biological Sciences.
[5] P. Fitzgerald,et al. Evidence for impaired long-term potentiation in schizophrenia and its relationship to motor skill learning. , 2008, Cerebral cortex.
[6] S. Gabriel,et al. Calibrating a coalescent simulation of human genome sequence variation. , 2005, Genome research.
[7] Paul Antoine Salin,et al. The suppression of brain cold-stable microtubules in mice induces synaptic defects associated with neuroleptic-sensitive behavioral disorders. , 2002, Genes & development.
[8] Laurent Excoffier,et al. Arlequin (version 3.0): An integrated software package for population genetics data analysis , 2005, Evolutionary bioinformatics online.
[9] M. Nagano,et al. An aromatase‐associated cytoplasmic inclusion, the “stigmoid body,” in the rat brain: II. Ultrastructure (with a review of its history and nomenclature) , 1993, The Journal of comparative neurology.
[10] J. Akey,et al. Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. , 2002, American journal of human genetics.
[11] K. Hornik,et al. Genome scan for susceptibility loci for schizophrenia and bipolar disorder , 2002, Biological Psychiatry.
[12] G. A. Watterson. The homozygosity test of neutrality. , 1978, Genetics.
[13] M. Daly,et al. Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. , 2004, American journal of human genetics.
[14] E. Gershon,et al. Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees. , 1997, Genomics.
[15] T. Sasaki,et al. Identification of human PDE7B, a cAMP-specific phosphodiesterase. , 2000, Biochemical and biophysical research communications.
[16] P. Visscher,et al. Rare chromosomal deletions and duplications increase risk of schizophrenia , 2008, Nature.
[17] David B. Goldstein,et al. A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia , 2009, PLoS genetics.
[18] W. James,et al. Schizophrenia as a Genetic Morphism , 1970, Nature.
[19] Mark Daly,et al. Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..
[20] S. Shaw,et al. A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees. , 2001, American journal of human genetics.
[21] Christopher P Austin,et al. DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation. , 2003, Human molecular genetics.
[22] P. Holmans,et al. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. , 2000, American journal of human genetics.
[23] Leena Peltonen,et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. , 2003, American journal of human genetics.
[24] Kathryn Cullen,et al. Limbic structures and networks in children and adolescents with schizophrenia. , 2007, Schizophrenia bulletin.
[25] W. Li,et al. Statistical tests of neutrality of mutations. , 1993, Genetics.
[26] Robert Zöchling,et al. Brain-derived neurotrophic factor and neurotrophin 3 in schizophrenic psychoses , 2001, Schizophrenia Research.
[27] S. Zeiler,et al. Development/Plasticity/Repair Brain-Derived Neurotrophic Factor Is Required for the Maintenance of Cortical Dendrites , 2022 .
[28] T. Matise,et al. NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees. , 1998, American journal of medical genetics.
[29] J. Sanjuán,et al. Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia , 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[30] Daniel Mathalon,et al. A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. , 2009, Schizophrenia bulletin.
[31] P. Muglia,et al. Association between the BDNF gene and schizophrenia , 2003, Molecular Psychiatry.
[32] W. Haenszel,et al. Statistical aspects of the analysis of data from retrospective studies of disease. , 1959, Journal of the National Cancer Institute.
[33] J. Palacios,et al. Alterations on phosphodiesterase type 7 and 8 isozyme mRNA expression in Alzheimer’s disease brains examined by in situ hybridization , 2003, Experimental Neurology.
[34] J. Lieberman,et al. Genomewide association for schizophrenia in the CATIE study: results of stage 1 , 2008, Molecular Psychiatry.
[35] Kevin L. Gunderson,et al. Highly parallel genomic assays , 2006, Nature Reviews Genetics.
[36] N. Andreasen,et al. Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q. , 1999, American journal of medical genetics.
[37] Kevin Thornton,et al. libsequence: a C++ class library for evolutionary genetic analysis , 2003, Bioinform..
[38] T. Crow. The ʻbig bangʼ theory of the origin of psychosis and the faculty of language , 2008, Schizophrenia Research.
[39] S. Mano,et al. Comparisons of site- and haplotype-frequency methods for detecting positive selection. , 2007, Molecular biology and evolution.
[40] C. Spencer,et al. Identification of loci associated with schizophrenia by genome-wide association and follow-up , 2008, Nature Genetics.
[41] E. Bertini,et al. AHI1 gene mutations cause specific forms of Joubert syndrome–related disorders , 2006, Annals of neurology.
[42] Doron Lancet,et al. AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia , 2006, European Journal of Human Genetics.
[43] J L Rapoport,et al. The neurodevelopmental model of schizophrenia: update 2005 , 2005, Molecular Psychiatry.
[44] T. Crow. Is schizophrenia the price that Homo sapiens pays for language? , 1997, Schizophrenia Research.
[45] G. A. Watterson. On the number of segregating sites in genetical models without recombination. , 1975, Theoretical population biology.
[46] Justin C. Fay,et al. Hitchhiking under positive Darwinian selection. , 2000, Genetics.
[47] L. Quintana-Murci,et al. Natural selection has driven population differentiation in modern humans , 2008, Nature Genetics.
[48] Christoph Lange,et al. PBAT: tools for family-based association studies. , 2004, American journal of human genetics.
[49] M Bleuler,et al. Dementia praecox oder die Gruppe der Schizophrenien: Eugen Bleuler , 1986, British Journal of Psychiatry.
[50] W. Maier,et al. The genetic epidemiology of schizophrenia and of schizophrenia spectrum disorders , 2000, European Archives of Psychiatry and Clinical Neuroscience.
[51] P. Smyth. Sun-spots and Terrestrial Magnetism , 1878, Nature.
[52] M C O'Donovan,et al. A genome-wide association study in 574 schizophrenia trios using DNA pooling , 2009, Molecular Psychiatry.
[53] Pablo V Gejman,et al. Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia. , 2004, American journal of human genetics.
[54] J. Bailey-Wilson,et al. Consanguineous matings in an Israeli-Arab community. , 1994, Archives of pediatrics & adolescent medicine.
[55] W. G. Hill,et al. Genetic Data Analysis II . By Bruce S. Weir, Sunderland, Massachusetts. Sinauer Associates, Inc.445 pages. ISBN 0-87893-902-4. , 1996 .
[56] Jianxin Shi,et al. Common variants on chromosome 6p22.1 are associated with schizophrenia , 2009, Nature.
[57] Bernard Lerer,et al. Genetics of schizophrenia: a review of linkage findings. , 2002, The Israel journal of psychiatry and related sciences.
[58] Tao Li,et al. Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women , 2008, PLoS genetics.
[59] A. Singleton,et al. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia , 2008, Science.
[60] I. Gottesman,et al. A single dominant gene still cannot account for the transmission of schizophrenia. , 1989, Archives of general psychiatry.
[61] M. Nei,et al. Mathematical model for studying genetic variation in terms of restriction endonucleases. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[62] J. Swanson,et al. The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus. , 2004, American journal of human genetics.
[63] H. Stefánsson,et al. Support for involvement of the AHI1 locus in schizophrenia , 2007, European Journal of Human Genetics.
[64] A. Clark,et al. Recent and ongoing selection in the human genome , 2007, Nature Reviews Genetics.
[65] Thomas W. Mühleisen,et al. Large recurrent microdeletions associated with schizophrenia , 2008, Nature.
[66] P. Visscher,et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. , 2003, American journal of human genetics.
[67] Jacqueline K. Wittke-Thompson,et al. Rational inferences about departures from Hardy-Weinberg equilibrium. , 2005, American journal of human genetics.
[68] D. Javitt,et al. Circuit-based framework for understanding neurotransmitter and risk gene interactions in schizophrenia , 2008, Trends in Neurosciences.
[69] R. J. Ferland,et al. Species differences in the expression of Ahi1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies , 2008, The Journal of comparative neurology.
[70] E. Robins,et al. Research diagnostic criteria: rationale and reliability. , 1978, Archives of general psychiatry.
[71] L. Girard,et al. Ahi-1, a Novel Gene Encoding a Modular Protein with WD40-Repeat and SH3 Domains, Is Targeted by the Ahi-1 and Mis-2 Provirus Integrations , 2002, Journal of Virology.
[72] W. Ewens,et al. The transmission/disequilibrium test: history, subdivision, and admixture. , 1995, American journal of human genetics.
[73] Paul J. Harrison,et al. For Personal Use. Only Reproduce with Permission from the Lancet Publishing Group. Genes for Schizophrenia? Recent Findings and Their Pathophysiological Implications , 2022 .
[74] R. Hudson,et al. A test of neutral molecular evolution based on nucleotide data. , 1987, Genetics.
[75] T. Shohat,et al. Trends in the frequencies of consanguineous marriages in the Israeli Arab community , 2000, Clinical genetics.
[76] Y. Hirayasu. Brain imaging in schizophrenia , 2007, Neuropathology : official journal of the Japanese Society of Neuropathology.
[77] P. McGuffin,et al. Linkage and associated studies of schizophrenia. , 2000, American journal of medical genetics.
[78] Stefan Schneider,et al. Arlequin (version 3.0): An integrated software package for population genetics data analysis , 2005 .
[79] E. Lander,et al. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease , 2003, Nature Genetics.
[80] A. Sampson,et al. Relationship of Brain-Derived Neurotrophic Factor and Its Receptor TrkB to Altered Inhibitory Prefrontal Circuitry in Schizophrenia , 2005, The Journal of Neuroscience.
[81] S. Tavaré,et al. Unrooted genealogical tree probabilities in the infinitely-many-sites model. , 1995, Mathematical biosciences.
[82] Francis J McMahon,et al. Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. , 2003, American journal of human genetics.
[83] J. Ott. Genetic data analysis II , 1997 .
[84] B. Kerem,et al. Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24 , 2003, Molecular Psychiatry.
[85] Y. Yuval,et al. Dominant inheritance in two families with familial Mediterranean fever (FMF). , 1995, American journal of medical genetics.
[86] John P A Ioannidis,et al. Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database , 2008, Nature Genetics.
[87] David Reich,et al. Detecting natural selection by empirical comparison to random regions of the genome , 2009, Human molecular genetics.
[88] N C Andreasen,et al. The family history method using diagnostic criteria. Reliability and validity. , 1977, Archives of general psychiatry.
[89] John P. Rice,et al. Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees , 2003, Biological Psychiatry.
[90] D. Weinberger. Implications of normal brain development for the pathogenesis of schizophrenia. , 1987, Archives of general psychiatry.
[91] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .
[92] Wendy S. Schackwitz,et al. Association of common variants in the Joubert syndrome gene (AHI1) with autism. , 2008, Human molecular genetics.
[93] J. R. Alexander,et al. A pedigree series for mapping disease genes in bipolar affective disorder: sampling, assessment, and analytic considerations. , 1994, Psychiatric genetics.
[94] A. Gori,et al. Use of RAPD and microsatellite (SSR) variation to assess genetic relationships among populations of tetraploid alfalfa, Medicago sativa , 2000 .
[95] S. K. Lo,et al. Reliability and Validity , 2020, International Encyclopedia of Human Geography.
[96] R Kucherlapati,et al. Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia , 2007, Molecular Psychiatry.
[97] Nancy C. Andreasen,et al. The family history method using diagnostic criteria , 1978 .
[98] A. Hoffer,et al. Schizophrenia as a Genetic Morphism , 1964, Nature.
[99] Christian von Mering,et al. STRING 8—a global view on proteins and their functional interactions in 630 organisms , 2008, Nucleic Acids Res..
[100] Pak Chung Sham,et al. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits , 2003, Bioinform..
[101] K. Johannesson,et al. Site‐specific genetic divergence in parallel hybrid zones suggests nonallopatric evolution of reproductive barriers , 2006, Molecular ecology.
[102] J. Delanghe,et al. Biological and clinical significance of haptoglobin polymorphism in humans. , 1996, Clinical chemistry.
[103] Christoph Lange,et al. PBAT: A comprehensive software package for genome-wide association analysis of complex family-based studies , 2005, Human Genomics.
[104] C. Walsh,et al. Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome , 2004, Nature Genetics.
[105] Kevin R. Thornton,et al. Inferring selection in partially sequenced regions. , 2008, Molecular biology and evolution.
[106] E. Walker,et al. Diagnostic and Statistical Manual of Mental Disorders , 2013 .
[107] M. Slatkin,et al. An investigation of the statistical power of neutrality tests based on comparative and population genetic data. , 2009, Molecular biology and evolution.
[108] G. Miller,et al. Resolving the paradox of common, harmful, heritable mental disorders: which evolutionary genetic models work best? , 2006, The Behavioral and brain sciences.
[109] Joseph A. Gogos,et al. Strong association of de novo copy number mutations with sporadic schizophrenia , 2008, Nature Genetics.
[110] H. Bandelt,et al. Median-joining networks for inferring intraspecific phylogenies. , 1999, Molecular biology and evolution.
[111] N. Bresolin,et al. Widespread balancing selection and pathogen-driven selection at blood group antigen genes. , 2009, Genome research.
[112] K. Gunderson,et al. Whole genome genotyping technologies on the BeadArray™ platform , 2007 .
[113] B. J. Williams,et al. Autism and Autistic Behavior in Joubert Syndrome , 1999, Journal of child neurology.
[114] B. Lerer,et al. Excitement and confusion on chromosome 6q: the challenges of neuropsychiatric genetics in microcosm , 2005, Molecular Psychiatry.
[115] D. Horrobin. Schizophrenia: The illness that made us human , 1998, Schizophrenia Research.
[116] S. Potkin,et al. Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia , 2009, Molecular Psychiatry.
[117] G. Abecasis,et al. A note on exact tests of Hardy-Weinberg equilibrium. , 2005, American journal of human genetics.
[118] S.. Sampling theory for neutral alleles in a varying environment , 2003 .
[119] John D. Storey,et al. Statistical significance for genomewide studies , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[120] Z. Rumboldt,et al. Absence of decussation of the superior cerebellar peduncles in patients with Joubert syndrome , 2008, American journal of medical genetics. Part A.
[121] A. Farmer,et al. The Strength of the Genetic Effect , 1994, British Journal of Psychiatry.
[122] I. Glass,et al. Joubert syndrome (and related disorders) (OMIM 213300) , 2007, European Journal of Human Genetics.
[123] M. First,et al. Nosology of chronic mood disorders. , 1996, The Psychiatric clinics of North America.
[124] Elaine Holmes,et al. Metabolic changes in schizophrenia and human brain evolution , 2008, Genome Biology.
[125] Xingshun Xu,et al. Huntingtin-associated protein 1 interacts with Ahi1 to regulate cerebellar and brainstem development in mice. , 2008, The Journal of clinical investigation.
[126] A. Andrieux,et al. STOP proteins. , 1999, Cell structure and function.
[127] Fred A. Wright,et al. Erratum: Genomewide association for schizophrenia in the CATIE study: Results of stage 1 (Molecular Psychiatry (2008) 13 (570-584) DOI: 10.1038/mp.2008.25) , 2009 .
[128] F. Tajima. Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. , 1989, Genetics.
[129] C. Ockleford,et al. Structure and function of the nematosome. , 1987, Journal of cell science.
[130] T. Kreis,et al. Identification and molecular characterization of E-MAP-115, a novel microtubule-associated protein predominantly expressed in epithelial cells , 1993, The Journal of cell biology.
[131] P. Visscher,et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder , 2009, Nature.
[132] M. Owen,et al. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. , 2003, American journal of human genetics.
[133] E M Wijsman,et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia , 2009, Molecular Psychiatry.
[134] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.