Michael Cuccaro

Associate Professor

  • 11604 Citations
1989 …2019
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Research Output 1992 2019

  • 11604 Citations
  • 123 Article
  • 1 Comment/debate
  • 1 Letter
2019
39 Citations (Scopus)

Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Alzheimer Disease Genetics Consortium (ADGC), European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE), & Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES), Mar 1 2019, In : Nature genetics. 51, 3, p. 414-430 17 p.

Research output: Contribution to journalArticle

Meta-Analysis
Immunity
Alzheimer Disease
Lipids
Serum Amyloid A Protein

Motivations for participation in Parkinson disease genetic research among hispanics versus non-hispanics

Nuytemans, K., Manrique, C. P., Uhlenberg, A., Scott, W. K., Cuccaro, M., Luca, C. C., Singer, C. & Vance, J. M., Jan 1 2019, In : Frontiers in Genetics. 10, JUN, 658.

Research output: Contribution to journalComment/debate

Open Access
Genetic Research
Hispanic Americans
Parkinson Disease
Research

RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways

Gardner, O. K., Wang, L., Van Booven, D., Whitehead, P. L., Hamilton-Nelson, K. L., Adams, L. D., Starks, T. D., Hofmann, N. K., Vance, J. M., Cuccaro, M., Martin, E. R., Byrd, G. S., Haines, J. L., Bush, W. S., Beecham, G. W., Pericak-Vance, M. A. & Griswold, A., Sep 15 2019, In : Human molecular genetics. 28, 18, p. 3053-3061 9 p.

Research output: Contribution to journalArticle

RNA Editing
Alzheimer Disease
African Americans
RNA Sequence Analysis
Transcriptome

The Puerto Rico Alzheimer disease initiative (PRADI): A multisource ascertainment approach

Feliciano-Astacio, B. E., Celis, K., Ramos, J., Rajabli, F., Adams, L. D., Rodriguez, A., Rodriguez, V., Bussies, P. L., Sierra, C., Manrique, P., Mena, P. R., Grana, A., Prough, M., Hamilton-Nelson, K. L., Feliciano, N., Chinea, A., Acosta, H., McCauley, J. L., Vance, J. M., Beecham, G. W. & 2 others, Pericak-Vance, M. A. & Cuccaro, M., Jan 1 2019, In : Frontiers in Genetics. 10, JUN, 538.

Research output: Contribution to journalArticle

Open Access
Puerto Rico
Alzheimer Disease
Hispanic Americans
Precision Medicine
Genetic Research
2018
4 Citations (Scopus)

Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations

Rajabli, F., Feliciano, B. E., Celis, K., Hamilton-Nelson, K. L., Whitehead, P. L., Adams, L. D., Bussies, P. L., Manrique, C. P., Rodriguez, A., Rodriguez, V., Starks, T., Byfield, G. E., Sierra Lopez, C. B., McCauley, J. L., Acosta, H., Chinea, A., Kunkle, B. W., Reitz, C., Farrer, L. A., Schellenberg, G. D. & 8 others, Vardarajan, B. N., Vance, J. M., Cuccaro, M., Martin, E. R., Haines, J. L., Byrd, G. S., Beecham, G. W. & Pericak-Vance, M. A., Dec 1 2018, In : PLoS Genetics. 14, 12, e1007791.

Research output: Contribution to journalArticle

Open Access
African American
Apolipoproteins E
African Americans
Alzheimer disease
ancestry
10 Citations (Scopus)

Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons

Derosa, B. A., El Hokayem, J., Artimovich, E., Garcia-Serje, C., Phillips, A. W., Van Booven, D., Nestor, J. E., Wang, L., Cuccaro, M., Vance, J. M., Pericak-Vance, M. A., Cukier, H. N., Nestor, M. W. & Dykxhoorn, D. M., Dec 1 2018, In : Scientific Reports. 8, 1, 8423.

Research output: Contribution to journalArticle

Autistic Disorder
Neurons
Induced Pluripotent Stem Cells
Gene Expression Profiling
Genes
2017
4 Citations (Scopus)

Early-onset Alzheimer disease and candidate risk genes involved in endolysosomal transport

Kunkle, B. W., Vardarajan, B. N., Naj, A. C., Whitehead, P. L., Rolati, S., Slifer, S., Carney, R. M., Cuccaro, M., Vance, J. M., Gilbert, J., Wang, L. S., Farrer, L. A., Reitz, C., Haines, J. L., Beecham, G. W., Martin, E. R., Schellenberg, G. D., Mayeux, R. P. & Pericak-Vance, M. A., Sep 1 2017, In : JAMA Neurology. 74, 9, p. 1113-1122 10 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Genes
Odds Ratio
National Institute of Neurological Disorders and Stroke
Communication Disorders

Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder

Griswold, A., van Booven, D., Cuccaro, M., Haines, J. L., Gilbert, J. & Pericak-Vance, M. A., Nov 18 2017, (Accepted/In press) In : Neurogenetics. p. 1-10 10 p.

Research output: Contribution to journalArticle

GABA Receptors
Autism Spectrum Disorder
Regulator Genes
gamma-Aminobutyric Acid
Open Reading Frames
35 Citations (Scopus)

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Anney, R. J. L., Ripke, S., Anttila, V., Grove, J., Holmans, P., Huang, H., Klei, L., Lee, P. H., Medland, S. E., Neale, B., Robinson, E., Weiss, L. A., Zwaigenbaum, L., Yu, T. W., Wittemeyer, K., Willsey, A. J., Wijsman, E. M., Werge, T., Wassink, T. H., Waltes, R. & 143 others, Walsh, C. A., Wallace, S., Vorstman, J. A. S., Vieland, V. J., Vicente, A. M., Vanengeland, H., Tsang, K., Thompson, A. P., Szatmari, P., Svantesson, O., Steinberg, S., Stefansson, K., Stefansson, H., State, M. W., Soorya, L., Silagadze, T., Scherer, S. W., Schellenberg, G. D., Sandin, S., Sanders, S. J., Saemundsen, E., Rouleau, G. A., Rogé, B., Roeder, K., Roberts, W., Reichert, J., Reichenberg, A., Rehnström, K., Regan, R., Poustka, F., Poultney, C. S., Piven, J., Pinto, D., Pericak-Vance, M. A., Pejovic-Milovancevic, M., Pedersen, M. G., Pedersen, C. B., Paterson, A. D., Parr, J. R., Pagnamenta, A. T., Oliveira, G., Nurnberger, J. I., Nordentoft, M., Murtha, M. T., Mouga, S., Mortensen, P. B., Mors, O., Morrow, E. M., Moreno-De-Luca, D., Monaco, A. P., Minshew, N., Merikangas, A., McMahon, W. M., McGrew, S. G., Mattheisen, M., Martsenkovsky, I., Martin, D. M., Mane, S. M., Magnusson, P., Magalhaes, T., Maestrini, E., Lowe, J. K., Lord, C., Levitt, P., Martin, C. L., Ledbetter, D. H., Leboyer, M., Lecouteur, A. S., Ladd-Acosta, C., Kolevzon, A., Klauck, S. M., Jacob, S., Iliadou, B., Hultman, C. M., Hougaard, D. M., Hertz-Picciotto, I., Hendren, R., Hansen, C. S., Haines, J. L., Guter, S. J., Grice, D. E., Green, J. M., Green, A., Goldberg, A. P., Gillberg, C., Gilbert, J., Gallagher, L., Freitag, C. M., Fombonne, E., Folstein, S. E., Fernandez, B., Fallin, M. D., Ercan-Sencicek, A. G., Ennis, S., Duque, F., Duketis, E., Delorme, R., Derubeis, S., Dejonge, M. V., Dawson, G., Cuccaro, M., Correia, C. T., Conroy, J., Conceição, I. C., Chiocchetti, A. G., Celestino-Soper, P. B. S., Casey, J., Cantor, R. M., Café, C., Bybjerg-Grauholm, J., Brennan, S., Bourgeron, T., Bolton, P. F., Bölte, S., Bolshakova, N., Betancur, C., Bernier, R., Beaudet, A. L., Battaglia, A., Bal, V. H., Baird, G., Bailey, A. J., Bækvad-Hansen, M., Bader, J. S., Bacchelli, E., Anagnostou, E., Amaral, D., Almeida, J., Børglum, A. D., Buxbaum, J. D., Chakravarti, A., Cook, E. H., Coon, H., Geschwind, D. H., Gill, M., Hallmayer, J., Palotie, A., Santangelo, S., Sutcliffe, J. S., Arking, D. E., Devlin, B., Daly, M. J. & Hakonarson, H., May 22 2017, In : Molecular Autism. 8, 1, 21.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Meta-Analysis
Schizophrenia
Genome
Genomics
100 Citations (Scopus)

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Psychiatric Genomics Consortium Autism Group & iPSYCH-Broad Autism Group, Jul 1 2017, In : Nature Genetics. 49, 7, p. 978-985 8 p.

Research output: Contribution to journalArticle

Autism Spectrum Disorder
Schizophrenia
Phenotype
4 Citations (Scopus)

Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease

Kunkle, B. W., Carney, R. M., Kohli, M. A., Naj, A. C., Hamilton-Nelson, K. L., Whitehead, P. L., Wang, L., Lang, R., Cuccaro, M., Vance, J. M., Byrd, G. S., Beecham, G. W., Gilbert, J., Martin, E. R., Haines, J. L. & Pericak-Vance, M. A., May 10 2017, In : Neuroscience Letters. 649, p. 124-129 6 p.

Research output: Contribution to journalArticle

Alzheimer Disease
African Americans
Population
Genes
3' Untranslated Regions
2016
17 Citations (Scopus)

ABCA7 frameshift deletion associated with Alzheimer disease in African Americans

Cukier, H. N., Kunkle, B. W., Vardarajan, B. N., Rolati, S., Hamilton-Nelson, K. L., Kohli, M. A., Whitehead, P. L., Dombroski, B. A., Van Booven, D., Lang, R., Dykxhoorn, D. M., Farrer, L. A., Cuccaro, M., Vance, J. M., Gilbert, J., Beecham, G. W., Martin, E. R., Carney, R. M., Mayeux, R., Schellenberg, G. D. & 3 others, Byrd, G. S., Haines, J. L. & Pericak-Vance, M. A., Jun 1 2016, In : Neurology: Genetics. 2, 3, e79.

Research output: Contribution to journalArticle

African Americans
Alzheimer Disease
Exome
Alleles
Odds Ratio
9 Citations (Scopus)
Autistic Disorder
Siblings
Dopamine
Genotype
Genes
7 Citations (Scopus)

Genetic polymorphisms related to behavioral approach and behavioral inhibition scales

Johnson, S. L., Carver, C. S., Joormann, J. & Cuccaro, M., Jan 1 2016, In : Personality and Individual Differences. 88, p. 251-255 5 p., 7047.

Research output: Contribution to journalArticle

Genetic Polymorphisms
Brain-Derived Neurotrophic Factor
Reward
Alleles
Inhibition (Psychology)
16 Citations (Scopus)

Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

Kohli, M. A., Cukier, H. N., Hamilton-Nelson, K. L., Rolati, S., Kunkle, B. W., Whitehead, P. L., Zuchner, S. L., Farrer, L. A., Martin, E. R., Beecham, G. W., Haines, J. L., Vance, J. M., Cuccaro, M., Gilbert, J., Schellenberg, G. D., Carney, R. M. & Pericak-Vance, M. A., Feb 1 2016, In : Neurology: Genetics. 2, 1, e41.

Research output: Contribution to journalArticle

Alzheimer Disease
Exome
Genes
Genetic Predisposition to Disease
Genome
17 Citations (Scopus)

SORL1 mutations in early- and late-onset Alzheimer disease

Cuccaro, M., Carney, R. M., Zhang, Y., Bohm, C., Kunkle, B. W., Vardarajan, B. N., Whitehead, P. L., Cukier, H. N., Mayeux, R., George-Hyslop, P. S. & Pericak-Vance, M. A., Jan 1 2016, In : Neurology: Genetics. 2, 6, e116.

Research output: Contribution to journalArticle

Alzheimer Disease
Amyloid
Protein Transport
Mutation
Exome
2015
13 Citations (Scopus)

A genetic analysis of the validity of the Hypomanic Personality Scale

Johnson, S. L., Carver, C. S., Joormann, J. & Cuccaro, M., May 1 2015, In : Bipolar Disorders. 17, 3, p. 331-339 9 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Personality
Anthozoa
Self Report
Genes
10 Citations (Scopus)

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

Kunkle, B. W., Jaworski, J., Barral, S., Vardarajan, B., Beecham, G. W., Martin, E. R., Cantwell, L. S., Partch, A., Bird, T. D., Raskind, W. H., Destefano, A. L., Carney, R. M., Cuccaro, M., Vance, J. M., Farrer, L. A., Goate, A. M., Foroud, T., Mayeux, R. P., Schellenberg, G. D., Haines, J. L. & 1 others, Pericak-Vance, M. A., 2015, (Accepted/In press) In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

Alzheimer Disease
Genome
Penetrance
Multigene Family
MicroRNAs
8 Citations (Scopus)

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

Hohman, T. J., Cooke-Bailey, J. N., Reitz, C., Jun, G., Naj, A., Beecham, G. W., Liu, Z., Carney, R. M., Vance, J. M., Cuccaro, M., Rajbhandary, R., Vardarajan, B. N., Wang, L. S., Valladares, O., Lin, C. F., Larson, E. B., Graff-Radford, N. R., Evans, D., De Jager, P. L., Crane, P. K. & 33 others, Buxbaum, J. D., Murrell, J. R., Raj, T., Ertekin-Taner, N., Logue, M. W., Baldwin, C. T., Green, R. C., Barnes, L. L., Cantwell, L. B., Fallin, M. D., Go, R. C. P., Griffith, P., Obisesan, T. O., Manly, J. J., Lunetta, K. L., Kamboh, M. I., Lopez, O. L., Bennett, D. A., Hardy, J., Hendrie, H. C., Hall, K. S., Goate, A. M., Lang, R., Byrd, G. S., Kukull, W. A., Foroud, T. M., Farrer, L. A., Martin, E. R., Pericak-Vance, M. A., Schellenberg, G. D., Mayeux, R., Haines, J. L. & Thornton-Wells, T. A., 2015, (Accepted/In press) In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

African Americans
Alzheimer Disease
Genome-Wide Association Study
98 Citations (Scopus)

Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder

Cross-Disorder Working Group of the Psychiatric Genomics Consortium, Feb 5 2015, In : American Journal of Human Genetics. 96, 2, p. 283-294 12 p.

Research output: Contribution to journalArticle

Major Depressive Disorder
Bipolar Disorder
Psychiatry
Schizophrenia
Sample Size
353 Citations (Scopus)

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

The Network and Pathway Analysis Subgroup of the Psychiatric Genomics Consortium & International Inflammatory Bowel Disease Genetics Consortium (IIBDGC), Feb 17 2015, In : Nature Neuroscience. 18, 2, p. 199-209 11 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Histones
Psychiatry
Post-Synaptic Density
Genomics
20 Citations (Scopus)

Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants

Griswold, A., Dueker, N. D., Van Booven, D., Rantus, J. A., Jaworski, J. M., Slifer, S. H., Schmidt, M., Hulme, W., Konidari, I., Whitehead, P. L., Cuccaro, M., Martin, E. R., Haines, J. L., Gilbert, J., Hussman, J. P. & Pericak-Vance, M. A., Jul 7 2015, In : Molecular Autism. 6, 1, 43.

Research output: Contribution to journalArticle

High-Throughput Nucleotide Sequencing
Genes
Genome-Wide Association Study
Autism Spectrum Disorder
Mutation
24 Citations (Scopus)

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis

Kozol, R., Cukier, H. N., Zou, B., Mayo, V., De Rubeis, S., Cai, G., Griswold, A., Whitehead, P. L., Haines, J. L., Gilbert, J., Cuccaro, M., Martin, E. R., Baker, J., Buxbaum, J. D., Pericak-Vance, M. A. & Dallman, J., Jul 15 2015, In : Human Molecular Genetics. 24, 14, p. 4006-4023 18 p., ddv138.

Research output: Contribution to journalArticle

Zebrafish
Autistic Disorder
Morphogenesis
Phenotype
Brain
2014
409 Citations (Scopus)

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Pinto, D., Delaby, E., Merico, D., Barbosa, M., Merikangas, A., Klei, L., Thiruvahindrapuram, B., Xu, X., Ziman, R., Wang, Z., Vorstman, J. A. S., Thompson, A., Regan, R., Pilorge, M., Pellecchia, G., Pagnamenta, A. T., Oliveira, B., Marshall, C. R., Magalhaes, T. R., Lowe, J. K. & 92 others, Howe, J. L., Griswold, A., Gilbert, J., Duketis, E., Dombroski, B. A., De Jonge, M. V., Cuccaro, M., Crawford, E. L., Correia, C. T., Conroy, J., Conceição, I. C., Chiocchetti, A. G., Casey, J. P., Cai, G., Cabrol, C., Bolshakova, N., Bacchelli, E., Anney, R., Gallinger, S., Cotterchio, M., Casey, G., Zwaigenbaum, L., Wittemeyer, K., Wing, K., Wallace, S., Van Engeland, H., Tryfon, A., Thomson, S., Soorya, L., Rogé, B., Roberts, W., Poustka, F., Mouga, S., Minshew, N., McInnes, L. A., McGrew, S. G., Lord, C., Leboyer, M., Le Couteur, A. S., Kolevzon, A., Jiménez González, P., Jacob, S., Holt, R., Guter, S., Green, J., Green, A., Gillberg, C., Fernandez, B. A., Duque, F., Delorme, R., Dawson, G., Chaste, P., Café, C., Brennan, S., Bourgeron, T., Bolton, P. F., Bölte, S., Bernier, R., Baird, G., Bailey, A. J., Anagnostou, E., Almeida, J., Wijsman, E. M., Vieland, V. J., Vicente, A. M., Schellenberg, G. D., Pericak-Vance, M. A., Paterson, A. D., Parr, J. R., Oliveira, G., Nurnberger, J. I., Monaco, A. P., Maestrini, E., Klauck, S. M., Hakonarson, H., Haines, J. L., Geschwind, D. H., Freitag, C. M., Folstein, S. E., Ennis, S., Coon, H., Battaglia, A., Szatmari, P., Sutcliffe, J. S., Hallmayer, J., Gill, M., Cook, E. H., Buxbaum, J. D., Devlin, B., Gallagher, L., Betancur, C. & Scherer, S. W., May 1 2014, In : American Journal of Human Genetics. 94, 5, p. 677-694 18 p.

Research output: Contribution to journalArticle

Genes
Fragile X Syndrome
Intellectual Disability
Synapses
Chromatin
93 Citations (Scopus)

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

Cukier, H. N., Dueker, N. D., Slifer, S. H., Lee, J. M., Whitehead, P. L., Lalanne, E., Leyva, N., Konidari, I., Gentry, R. C., Hulme, W. F., Booven, D. V., Mayo, V., Hofmann, N. K., Schmidt, M., Martin, E. R., Haines, J. L., Cuccaro, M., Gilbert, J. & Pericak-Vance, M. A., Jan 10 2014, In : Molecular Autism. 5, 1, 1.

Research output: Contribution to journalArticle

Exome
Autistic Disorder
Genes
Neurodevelopmental Disorders
Autism Spectrum Disorder
12 Citations (Scopus)

Genetic testing and corresponding services among individuals with autism spectrum disorder (ASD)

Cuccaro, M., Czape, K., Alessandri, M., Lee, J., Deppen, A. R., Bendik, E., Dueker, N., Nations, L., Pericak-Vance, M. A. & Hahn, S., Jan 1 2014, In : American Journal of Medical Genetics, Part A. 164, 10, p. 2592-2600 9 p.

Research output: Contribution to journalArticle

Genetic Testing
Genetic Services
Referral and Consultation
Parents
Costs and Cost Analysis
17 Citations (Scopus)

The Autism Simplex Collection: An international, expertly phenotyped autism sample for genetic and phenotypic analyses

Buxbaum, J. D., Bolshakova, N., Brownfeld, J. M., Anney, R. J. L., Bender, P., Bernier, R., Cook, E. H., Coon, H., Cuccaro, M., Freitag, C. M., Hallmayer, J., Geschwind, D., Klauck, S. M., Nurnberger, J. I., Oliveira, G., Pinto, D., Poustka, F., Scherer, S. W., Shih, A., Sutcliffe, J. S. & 4 others, Szatmari, P., Vicente, A. M., Vieland, V. & Gallagher, L., Jan 1 2014, In : Molecular Autism. 5, 1, 34.

Research output: Contribution to journalArticle

Autistic Disorder
National Institutes of Health (U.S.)
National Institute of Mental Health (U.S.)
Exome
Genetic Research
37 Citations (Scopus)

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Hadley, D., Wu, Z. L., Kao, C., Kini, A., Mohamed-Hadley, A., Thomas, K., Vazquez, L., Qiu, H., Mentch, F., Pellegrino, R., Kim, C., Connolly, J., Glessner, J., Hakonarson, H., Pinto, D., Merikangas, A., Klei, L., Vorstman, J. A. S., Thompson, A., Regan, R. & 78 others, Pagnamenta, A. T., Oliveira, B., Magalhaes, T. R., Gilbert, J., Duketis, E., De Jonge, M. V., Cuccaro, M., Correia, C. T., Conroy, J., Conceiça, I. C., Chiocchetti, A. G., Casey, J. P., Bolshakova, N., Bacchelli, E., Anney, R., Zwaigenbaum, L., Wittemeyer, K., Wallace, S., Van Engeland, H., Soorya, L., Rogé, B., Roberts, W., Poustka, F., Mouga, S., Minshew, N., McGrew, S. G., Lord, C., Leboyer, M., Le Couteur, A. S., Kolevzon, A., Jacob, S., Guter, S., Green, J., Green, A., Gillberg, C., Fernandez, B. A., Duque, F., Delorme, R., Dawson, G., Brennan, S., Bourgeron, T., Bolton, P. F., Bölte, S., Bernier, R., Baird, G., Bailey, A. J., Anagnostou, E., Wijsman, E. M., Vieland, V. J., Vicente, A. M., Schellenberg, E. D., Pericak-Vance, M. A., Paterson, A. D., Parr, J. R., Oliveira, G., Almeida, J., Café, C., Nurnberger, J. I., Monaco, A. P., Maestrini, E., Klauck, S. M., Haines, J. L., Geschwind, D. H., Freitag, C. M., Folstein, S. E., Ennis, S., Coon, H., Battaglia, A., Szatmari, P., Sutcliffe, J. S., Hallmayer, J., Gill, M., Cook, E. H., Buxbaum, J. D., Devlin, B., Gallagher, L., Betancur, C. & Scherer, S. W., Jun 13 2014, In : Nature Communications. 5, 4074.

Research output: Contribution to journalArticle

glutamates
Metabotropic Glutamate Receptors
Autistic Disorder
genes
Genes
11 Citations (Scopus)

Variation in oxytocin receptor gene (OXTR) polymorphisms is associated with emotional and behavioral reactions to betrayal

Tabak, B. A., McCullough, M., Carver, C. S., Pedersen, E. J. & Cuccaro, M., Jan 1 2014, In : Social Cognitive and Affective Neuroscience. 9, 6, p. 810-816 7 p., nst042.

Research output: Contribution to journalArticle

Oxytocin Receptors
Haplotypes
Genes
Anger
Cognition
2013
18 Citations (Scopus)

Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders

Hadjixenofontos, A., Schmidt, M., Whitehead, P. L., Konidari, I., Hedges, D. J., Wright, H. H., Abramson, R. K., Menon, R., Williams, S. M., Cuccaro, M., Haines, J. L., Gilbert, J., Pericak-Vance, M. A., Martin, E. R. & McCauley, J. L., Jan 1 2013, In : Annals of Human Genetics. 77, 1, p. 9-21 13 p.

Research output: Contribution to journalArticle

Mitochondrial DNA
Autistic Disorder
Autism Spectrum Disorder
Genome-Wide Association Study
Fathers
1097 Citations (Scopus)

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E., Asherson, P. & 350 others, Azevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S. E., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E. B., Black, D. W., Blackwood, D. H. R., Bloss, C. S., Boehnke, M., Boomsma, D. I., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N. G., Buitelaar, J. K., Bunney, W. E., Buxbaum, J. D., Byerley, W. F., Byrne, E. M., Caesar, S., Cahn, W., Cantor, R. M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Cloninger, C. R., Collier, D. A., Cook, E. H., Coon, H., Cormand, B., Corvin, A., Coryell, W. H., Craig, D. W., Craig, I. W., Crosbie, J., Cuccaro, M., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., De Geus, E. J., Degenhardt, F., Djurovic, S., Donohoe, G. J., Doyle, A. E., Duan, J., Dudbridge, F., Duketis, E., Ebstein, R. P., Edenberg, H. J., Elia, J., Ennis, S., Etain, B., Fanous, A., Farmer, A. E., Ferrier, I. N., Flickinger, M., Fombonne, E., Foroud, T., Frank, J., Franke, B., Fraser, C., Freedman, R., Freimer, N. B., Freitag, C. M., Friedl, M., Frisén, L., Gallagher, L., Gejman, P. V., Georgieva, L., Gershon, E. S., Geschwind, D. H., Giegling, I., Gill, M., Gordon, S. D., Gordon-Smith, K., Green, E. K., Greenwood, T. A., Grice, D. E., Gross, M., Grozeva, D., Guan, W., Gurling, H., De Haan, L., Haines, J. L., Hakonarson, H., Hallmayer, J., Hamilton, S. P., Hamshere, M. L., Hansen, T. F., Hartmann, A. M., Hautzinger, M., Heath, A. C., Henders, A. K., Herms, S., Hickie, I. B., Hipolito, M., Hoefels, S., Holmans, P. A., Holsboer, F., Hoogendijk, W. J., Hottenga, J. J., Hultman, C. M., Hus, V., Ingason, A., Ising, M., Jamain, S., Jones, E. G., Jones, I., Jones, L., Tzeng, J. Y., Kähler, A. K., Kahn, R. S., Kandaswamy, R., Keller, M. C., Kennedy, J. L., Kenny, E., Kent, L., Kim, Y., Kirov, G. K., Klauck, S. M., Klei, L., Knowles, J. A., Kohli, M. A., Koller, D. L., Konte, B., Korszun, A., Krabbendam, L., Krasucki, R., Kuntsi, J., Kwan, P., Landén, M., Långström, N., Lathrop, M., Lawrence, J., Lawson, W. B., Leboyer, M., Ledbetter, D. H., Lee, P. H., Lencz, T., Lesch, K. P., Levinson, D. F., Lewis, C. M., Li, J., Lichtenstein, P., Lieberman, J. A., Lin, D. Y., Linszen, D. H., Liu, C., Lohoff, F. W., Loo, S. K., Lord, C., Lowe, J. K., Lucae, S., Macintyre, D. J., Madden, P. A. F., Maestrini, E., Magnusson, P. K. E., Mahon, P. B., Maier, W., Malhotra, A. K., Mane, S. M., Martin, C. L., Martin, N. G., Mattheisen, M., Matthews, K., Mattingsdal, M., Mccarroll, S. A., Mcghee, K. A., Mcgough, J. J., Mcgrath, P. J., Mcguffin, P., Mcinnis, M. G., Mcintosh, A., Mckinney, R., Mclean, A. W., Mcmahon, F. J., Mcmahon, W. M., Mcquillin, A., Medeiros, H., Medland, S. E., Meier, S., Melle, I., Meng, F., Meyer, J., Middeldorp, C. M., Middleton, L., Milanova, V., Miranda, A., Monaco, A. P., Montgomery, G. W., Moran, J. L., Moreno-De-Luca, D., Morken, G., Morris, D. W., Morrow, E. M., Moskvina, V., Muglia, P., Mühleisen, T. W., Muir, W. J., Müller-Myhsok, B., Murtha, M., Myers, R. M., Myin-Germeys, I., Neale, M. C., Nelson, S. F., Nievergelt, C. M., Nikolov, I., Nimgaonkar, V., Nolen, W. A., Nöthen, M. M., Nurnberger, J. I., Nwulia, E. A., Nyholt, D. R., O'dushlaine, C., Oades, R. D., Olincy, A., Oliveira, G., Olsen, L., Ophoff, R. A., Osby, U., Owen, M. J., Palotie, A., Parr, J. R., Paterson, A. D., Pato, C. N., Pato, M. T., Penninx, B. W., Pergadia, M. L., Pericak-Vance, M. A., Pickard, B. S., Pimm, J., Piven, J., Posthuma, D., Potash, J. B., Poustka, F., Propping, P., Puri, V., Quested, D. J., Quinn, E. M., Ramos-Quiroga, J. A., Rasmussen, H. B., Raychaudhuri, S., Rehnström, K., Reif, A., Ribasés, M., Rice, J. P., Rietschel, M., Roeder, K., Roeyers, H., Rossin, L., Rothenberger, A., Rouleau, G., Ruderfer, D., Rujescu, D., Sanders, A. R., Sanders, S. J., Santangelo, S. L., Sergeant, J. A., Schachar, R., Schalling, M., Schatzberg, A. F., Scheftner, W. A., Schellenberg, G. D., Scherer, S. W., Schork, N. J., Schulze, T. G., Schumacher, J., Schwarz, M., Scolnick, E., Scott, L. J., Shi, J., Shilling, P. D., Shyn, S. I., Silverman, J. M., Slager, S. L., Smalley, S. L., Smit, J. H., Smith, E. N., Sonuga-Barke, E. J. S., St. Clair, D., State, M., Steffens, M., Steinhausen, H. C., Strauss, J. S., Strohmaier, J., Stroup, T. S., Sutcliffe, J. S., Szatmari, P., Szelinger, S., Thirumalai, S., Thompson, R. C., Todorov, A. A., Tozzi, F., Treutlein, J., Uhr, M., Van Den Oord, E. J. C. G., Van Grootheest, G., Van Os, J., Vicente, A. M., Vieland, V. J., Vincent, J. B., Visscher, P. M., Walsh, C. A., Wassink, T. H., Watson, S. J., Weissman, M. M., Werge, T., Wienker, T. F., Wijsman, E. M., Willemsen, G., Williams, N., Willsey, A. J., Witt, S. H., Xu, W., Young, A. H., Yu, T. W., Zammit, S., Zandi, P. P., Zhang, P., Zitman, F. G., Zöllner, S., Devlin, B., Kelsoe, J. R., Sklar, P., Daly, M. J., O'donovan, M. C., Craddock, N., Sullivan, P. F., Smoller, J. W., Kendler, K. S. & Wray, N. R., Sep 1 2013, In : Nature Genetics. 45, 9, p. 984-994 11 p.

Research output: Contribution to journalArticle

Major Depressive Disorder
Single Nucleotide Polymorphism
Psychiatry
Schizophrenia
Bipolar Disorder
4 Citations (Scopus)

Genomic Signatures of a Global Fitness Index in a Multi-Ethnic Cohort of Women

Rampersaud, E., Nathanson, L., Farmer, J., Meshbane, K., Belton, R. L., Dressen, A., Cuccaro, M., Musto, A., Daunert, S., Deo, S. K., Hudson, N., Vance, J. M., Seo, D. M., Mendez, A. J., Dykxhoorn, D. M., Pericak-Vance, M. A. & Goldschmidt-Clermont, P., Mar 1 2013, In : Annals of Human Genetics. 77, 2, p. 147-157 11 p.

Research output: Contribution to journalArticle

Genes
Exercise
Sedentary Lifestyle
Messenger RNA
Oxidative Phosphorylation
125 Citations (Scopus)

Reconstructing the Population Genetic History of the Caribbean

Moreno-Estrada, A., Gravel, S., Zakharia, F., McCauley, J. L., Byrnes, J. K., Gignoux, C. R., Ortiz-Tello, P. A., Martínez, R. J., Hedges, D. J., Morris, R. W., Eng, C., Sandoval, K., Acevedo-Acevedo, S., Norman, P. J., Layrisse, Z., Parham, P., Martínez-Cruzado, J. C., Burchard, E. G., Cuccaro, M., Martin, E. R. & 1 others, Bustamante, C. D., Nov 1 2013, In : PLoS Genetics. 9, 11, e1003925.

Research output: Contribution to journalArticle

Population Genetics
ancestry
population genetics
North American Indians
genome
2012
117 Citations (Scopus)

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Casey, J. P., Magalhaes, T., Conroy, J. M., Regan, R., Shah, N., Anney, R., Shields, D. C., Abrahams, B. S., Almeida, J., Bacchelli, E., Bailey, A. J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bolton, P. F., Bourgeron, T., Brennan, S., Cali, P., Correia, C. & 106 others, Corsello, C., Coutanche, M., Dawson, G., De Jonge, M., Delorme, R., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Foley, S., Fombonne, E., Freitag, C. M., Gilbert, J., Gillberg, C., Glessner, J. T., Green, J., Guter, S. J., Hakonarson, H., Holt, R., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S. M., Kolevzon, A., Lamb, J. A., Leboyer, M., Couteur, A. L., Leventhal, B. L., Lord, C., Lund, S. C., Maestrini, E., Mantoulan, C., Marshall, C. R., McConachie, H., McDougle, C. J., McGrath, J., McMahon, W. M., Merikangas, A., Miller, J., Minopoli, F., Mirza, G. K., Munson, J., Nelson, S. F., Nygren, G., Oliveira, G., Pagnamenta, A. T., Papanikolaou, K., Parr, J. R., Parrini, B., Pickles, A., Pinto, D., Piven, J., Posey, D. J., Poustka, A., Poustka, F., Ragoussis, J., Roge, B., Rutter, M. L., Sequeira, A. F., Soorya, L., Sousa, I., Sykes, N., Stoppioni, V., Tancredi, R., Tauber, M., Thompson, A. P., Thomson, S., Tsiantis, J., Van Engeland, H., Vincent, J. B., Volkmar, F., Vorstman, J. A. S., Wallace, S., Wang, K., Wassink, T. H., White, K., Wing, K., Wittemeyer, K., Yaspan, B. L., Zwaigenbaum, L., Betancur, C., Buxbaum, J. D., Cantor, R. M., Cook, E. H., Coon, H., Cuccaro, M., Geschwind, D. H., Haines, J. L., Hallmayer, J., Monaco, A. P., Nurnberger, J. I., Pericak-Vance, M. A., Schellenberg, G. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P., Vieland, V. J., Wijsman, E. M., Green, A., Gill, M., Gallagher, L., Vicente, A. & Ennis, S., Apr 1 2012, In : Human Genetics. 131, 4, p. 565-579 15 p.

Research output: Contribution to journalArticle

Haplotypes
Genes
Autism Spectrum Disorder
Aptitude
Genetic Heterogeneity
42 Citations (Scopus)

Derivation of autism spectrum disorder-specific induced pluripotent stem cells from peripheral blood mononuclear cells

DeRosa, B. A., Van Baaren, J. M., Dubey, G. K., Lee, J. M., Cuccaro, M., Vance, J. M., Pericak-Vance, M. A. & Dykxhoorn, D. M., May 10 2012, In : Neuroscience Letters. 516, 1, p. 9-14 6 p.

Research output: Contribution to journalArticle

Induced Pluripotent Stem Cells
Blood Cells
Stem Cells
Biopsy
Skin
95 Citations (Scopus)

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways

Griswold, A., Ma, D., Cukier, H. N., Nations, L. D., Schmidt, M., Chung, R. H., Jaworski, J. M., Salyakina, D., Konidari, I., Whitehead, P. L., Wright, H. H., Abramson, R. K., Williams, S. M., Menon, R., Martin, E. R., Haines, J. L., Gilbert, J., Cuccaro, M. & Pericak-Vance, M. A., Aug 1 2012, In : Human Molecular Genetics. 21, 15, p. 3513-3523 11 p., dds164.

Research output: Contribution to journalArticle

GABA Receptors
Genes
GABA Plasma Membrane Transport Proteins
Neural Pathways
Genetic Loci
19 Citations (Scopus)

Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci

Hedges, D. J., Hamilton-Nelson, K. L., Sacharow, S. J., Nations, L., Beecham, G. W., Kozhekbaeva, Z. M., Butler, B. L., Cukier, H. N., Whitehead, P. L., Ma, D., Jaworski, J. M., Nathanson, L., Lee, J. M., Hauser, S. L., Oksenberg, J. R., Cuccaro, M., Haines, J. L., Gilbert, J. & Pericak-Vance, M. A., May 22 2012, In : Molecular Autism. 3, 1, 2.

Research output: Contribution to journalArticle

Autistic Disorder
GABA Receptors
gamma-Aminobutyric Acid
Genes
Polymerase Chain Reaction
21 Citations (Scopus)

Exploring the relationship between autism spectrum disorder and epilepsy using latent class cluster analysis

Cuccaro, M., Tuchman, R. F., Hamilton, K. L., Wright, H. H., Abramson, R. K., Haines, J. L., Gilbert, J. & Pericak-Vance, M. A., Aug 1 2012, In : Journal of Autism and Developmental Disorders. 42, 8, p. 1630-1641 12 p.

Research output: Contribution to journalArticle

Cluster Analysis
Epilepsy
Phenotype
Language Development
Autism Spectrum Disorder
21 Citations (Scopus)

Genome-Wide Association and Linkage Study in the Amish Detects a Novel Candidate Late-Onset Alzheimer Disease Gene

Cummings, A. C., Jiang, L., Velez Edwards, D. R., McCauley, J. L., Laux, R., Mcfarland, L. L., Fuzzell, D., Knebusch, C., Caywood, L., Reinhart-Mercer, L., Nations, L., Gilbert, J., Konidari, I., Tramontana, M., Cuccaro, M., Scott, W. K., Pericak-Vance, M. A. & Haines, J. L., Sep 1 2012, In : Annals of Human Genetics. 76, 5, p. 342-351 10 p.

Research output: Contribution to journalArticle

Amish
Genome-Wide Association Study
Alzheimer Disease
Single Nucleotide Polymorphism
Genome
220 Citations (Scopus)

Individual common variants exert weak effects on the risk for autism spectrum disorderspi

Anney, R., Klei, L., Pinto, D., Almeida, J., Bacchelli, E., Baird, G., Bolshakova, N., Bölte, S., Bolton, P. F., Bourgeron, T., Brennan, S., Brian, J., Casey, J., Conroy, J., Correia, C., Corsello, C., Crawford, E. L., De jonge, M., Delorme, R., Duketis, E. & 117 others, Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Fombonne, E., Gilbert, J., Gillberg, C., Glessner, J. T., Green, A., Green, J., Guter, S. J., Heron, E. A., Holt, R., Howe, J. L., Hughes, G., Hus, V., Igliozzi, R., Jacob, S., Kenny, G. P., Kim, C., Kolevzon, A., Kustanovich, V., Lajonchere, C. M., Lamb, J. A., Law-Smith, M., Leboyer, M., Le couteur, A., Leventhal, B. L., Liu, X. Q., Lombard, F., Lord, C., Lotspeich, L., Lund, S. C., Magalhaes, T. R., Mantoulan, C., McDougle, C. J., Melhem, N. M., Merikangas, A., Minshew, N. J., Mirza, G. K., Munson, J., Noakes, C., Nygren, G., Papanikolaou, K., Pagnamenta, A. T., Parrini, B., Paton, T., Pickles, A., Posey, D. J., Poustka, F., Ragoussis, J., Regan, R., Roberts, W., Roeder, K., Roge, B., Rutter, M. L., Schlitt, S., Shah, N., Sheffield, V. C., Soorya, L., Sousa, I., Stoppioni, V., Sykes, N., Tancredi, R., Thompson, A. P., Thomson, S., Tryfon, A., Tsiantis, J., Van Engeland, H., Vincent, J. B., Volkmar, F., Vorstman, J. A. S., Wallace, S., Wing, K., Wittemeyer, K., Wood, S., Zurawiecki, D., Zwaigenbaum, L., Bailey, A. J., Battaglia, A., Cantor, R. M., Coon, H., Cuccaro, M., Dawson, G., Ennis, S., Freitag, C. M., Geschwind, D. H., Haines, J. L., Klauck, S. M., Mcmahon, W. M., Maestrini, E., Miller, J., Monaco, A. P., Nelson, S. F., Nurnberger, J. I., Oliveira, G., Parr, J. R., Pericak-Vance, M. A., Piven, J., Schellenberg, G. D., Scherer, S. W., Vicente, A. M., Wassink, T. H., Wijsman, E. M., Betancur, C., Buxbaum, J. D., Cook, E. H., Gallagher, L., Gill, M., Hallmayer, J., Paterson, A. D., Sutcliffe, J. S., Szatmari, P., Vieland, V. J., Hakonarson, H. & Devlin, B., Nov 1 2012, In : Human Molecular Genetics. 21, 21, p. 4781-4792 12 p., dds301.

Research output: Contribution to journalArticle

Autistic Disorder
Single Nucleotide Polymorphism
Alleles
Genome
Language Development
42 Citations (Scopus)

The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1

Cukier, H. N., Lee, J. M., Ma, D., Young, J., Mayo, V., Butler, B. L., Ramsook, S. S., Rantus, J. A., Abrams, A. J., Whitehead, P. L., Wright, H. H., Abramson, R. K., Haines, J. L., Cuccaro, M., Pericak-Vance, M. A. & Gilbert, J., Dec 1 2012, In : Autism Research. 5, 6, p. 385-397 13 p.

Research output: Contribution to journalArticle

Autistic Disorder
Genes
Rett Syndrome
Developmental Disabilities
Methyl CpG Binding Domain
2011
12 Citations (Scopus)

A de novo 1.5Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis

Griswold, A., Ma, D., Sacharow, S. J., Robinson, J. L., Jaworski, J. M., Wright, H. H., Abramson, R. K., Lybæk, H., Øyen, N., Cuccaro, M., Gilbert, J. & Pericak-Vance, M. A., Jun 1 2011, In : Autism Research. 4, 3, p. 221-227 7 p.

Research output: Contribution to journalArticle

Autistic Disorder
Chromosomes
Methylenetetrahydrofolate Dehydrogenase (NADP)
Spectrin
Cytoskeletal Proteins
100 Citations (Scopus)

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

Hussman, J. P., Chung, R. H., Griswold, A., Jaworski, J. M., Salyakina, D., Ma, D., Konidari, I., Whitehead, P. L., Vance, J. M., Martin, E. R., Cuccaro, M., Gilbert, J., Haines, J. L. & Pericak-Vance, M. A., Dec 1 2011, In : Molecular Autism. 2, 1, 1.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Autistic Disorder
Noise
Genes
Aptitude
21 Citations (Scopus)

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males

Chung, R. H., Ma, D., Wang, K., Hedges, D. J., Jaworski, J. M., Gilbert, J., Cuccaro, M., Wright, H. H., Abramson, R. K., Konidari, I., Whitehead, P. L., Schellenberg, G. D., Hakonarson, H., Haines, J. L., Pericak-Vance, M. A. & Martin, E. R., Dec 1 2011, In : Molecular Autism. 2, 1, 18.

Research output: Contribution to journalArticle

X Chromosome
Autistic Disorder
Genes
Meta-Analysis
Single Nucleotide Polymorphism
41 Citations (Scopus)

Childhood adversity interacts separately with 5-HTTLPR and BDNF to predict lifetime depression diagnosis

Carver, C. S., Johnson, S. L., Joormann, J., Lemoult, J. & Cuccaro, M., Jul 1 2011, In : Journal of Affective Disorders. 132, 1-2, p. 89-93 5 p.

Research output: Contribution to journalArticle

Brain-Derived Neurotrophic Factor
Serotonin Plasma Membrane Transport Proteins
Diagnostic and Statistical Manual of Mental Disorders
Self Report
Genotype
40 Citations (Scopus)

Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk

Salyakina, D., Cukier, H. N., Lee, J. M., Sacharow, S., Nations, L. D., Ma, D., Jaworski, J. M., Konidari, I., Whitehead, P. L., Wright, H. H., Abramson, R. K., Williams, S. M., Menon, R., Haines, J. L., Gilbert, J., Cuccaro, M. & Pericak-Vance, M. A., Oct 7 2011, In : PLoS One. 6, 10, e26049.

Research output: Contribution to journalArticle

Autistic Disorder
Nucleotides
Polymorphism
Genes
single nucleotide polymorphism
71 Citations (Scopus)

Epilepsy and autism: Neurodevelopmental perspective

Tuchman, R. & Cuccaro, M., Aug 1 2011, In : Current Neurology and Neuroscience Reports. 11, 4, p. 428-434 7 p.

Research output: Contribution to journalArticle

Autistic Disorder
Epilepsy
Phenotype
Intellectual Disability
Seizures
5 Citations (Scopus)

Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21

Cukier, H. N., Salyakina, D., Blankstein, S. F., Robinson, J. L., Sacharow, S., Ma, D., Wright, H. H., Abramson, R. K., Menon, R., Williams, S. M., Haines, J. L., Cuccaro, M., Gilbert, J. & Pericak-Vance, M. A., Jun 1 2011, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 156, 4, p. 493-501 9 p.

Research output: Contribution to journalArticle

Autistic Disorder
Base Pairing
Asperger Syndrome
Genes
Autoantigens
2010
376 Citations (Scopus)

A genome-wide scan for common alleles affecting risk for autism

Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., Sykes, N., Pagnamenta, A. T., Almeida, J., Bacchelli, E., Bailey, A. J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bölte, S., Bolton, P. F., Bourgeron, T. & 146 others, Brennan, S., Brian, J., Carson, A. R., Casallo, G., Casey, J., Chu, S. H., Cochrane, L., Corsello, C., Crawford, E. L., Crossett, A., Dawson, G., de Jonge, M., Delorme, R., Drmic, I., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Fombonne, E., Freitag, C. M., Gilbert, J., Gillberg, C., Glessner, J. T., Goldberg, J., Green, J., Guter, S. J., Hakonarson, H., Heron, E. A., Hill, M., Holt, R., Howe, J. L., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S. M., Kolevzon, A., Korvatska, O., Kustanovich, V., Lajonchere, C. M., Lamb, J. A., Laskawiec, M., Leboyer, M., Le Couteur, A., Leventhal, B. L., Lionel, A. C., Liu, X. Q., Lord, C., Lotspeich, L., Lund, S. C., Maestrini, E., Mahoney, W., Mantoulan, C., Marshall, C. R., McConachie, H., McDougle, C. J., McGrath, J., McMahon, W. M., Melhem, N. M., Merikangas, A., Migita, O., Minshew, N. J., Mirza, G. K., Munson, J., Nelson, S. F., Noakes, C., Noor, A., Nygren, G., Oliveira, G., Papanikolaou, K., Parr, J. R., Parrini, B., Paton, T., Pickles, A., Piven, J., Posey, D. J., Poustka, A., Poustka, F., Prasad, A., Ragoussis, J., Renshaw, K., Rickaby, J., Roberts, W., Roeder, K., Roge, B., Rutter, M. L., Bierut, L. J., Rice, J. P., Salt, J., Sansom, K., Sato, D., Segurado, R., Senman, L., Shah, N., Sheffield, V. C., Soorya, L., Sousa, I., Stoppioni, V., Strawbridge, C., Tancredi, R., Tansey, K., Thiruvahindrapduram, B., Thompson, A. P., Thomson, S., Tryfon, A., Tsiantis, J., van Engeland, H., Vincent, J. B., Volkmar, F., Wallace, S., Wang, K., Wang, Z., Wassink, T. H., Wing, K., Wittemeyer, K., Wood, S., Yaspan, B. L., Zurawiecki, D., Zwaigenbaum, L., Betancur, C., Buxbaum, J. D., Cantor, R. M., Cook, E. H., Coon, H., Cuccaro, M., Gallagher, L., Geschwind, D. H., Gill, M., Haines, J. L., Miller, J., Monaco, A. P., Nurnberger, J. I., Paterson, A. D., Pericak-Vance, M. A., Schellenberg, G. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P., Vicente, A. M., Vieland, V. J., Wijsman, E. M., Devlin, B., Ennis, S. & Hallmayer, J., Jul 27 2010, In : Human Molecular Genetics. 19, 20, p. 4072-4082 11 p., ddq307.

Research output: Contribution to journalArticle

Autistic Disorder
Alleles
Genome
Single Nucleotide Polymorphism
Genotype
34 Citations (Scopus)

Association and gene-gene interaction of SLC6A4 and ITGB3 in autism

Ma, D. Q., Rabionet, R., Konidari, I., Jaworski, J., Cukier, H. N., Wright, H. H., Abramson, R. K., Gilbert, J., Cuccaro, M., Pericak-Vance, M. A. & Martin, E. R., Mar 1 2010, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153, 2, p. 477-483 7 p.

Research output: Contribution to journalArticle

Autistic Disorder
History
Genes
Genetic Heterogeneity
Multifactor Dimensionality Reduction