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1دورية أكاديمية
المؤلفون: Ravinesh A Kumar, Christian R Marshall, Judith A Badner, Timothy D Babatz, Zohar Mukamel, Kimberly A Aldinger, Jyotsna Sudi, Camille W Brune, Gerald Goh, Samer Karamohamed, James S Sutcliffe, Edwin H Cook, Daniel H Geschwind, William B Dobyns, Stephen W Scherer, Susan L Christian
المصدر: PLoS ONE, Vol 4, Iss 2, p e4582 (2009)
وصف الملف: electronic resource
العلاقة: http://europepmc.org/articles/PMC2644762?pdf=renderTest; https://doaj.org/toc/1932-6203Test
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2دورية أكاديمية
المؤلفون: Joseph T. Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E. Kim, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Patrick M. A. Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James Flory, Frederick Otieno, Maria Garris, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, J. Mcdougle, Lea K. Davis, Judith Miller, David J. Posey, Shana Michaels, Er Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, T. Schultz, Geraldine Dawson, Thomas Owley, William M. Mcmahon, Thomas H, John A. Sweeney, John I. Nurnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F. A. Grant, Maja Bucan, Edwin H. Cook, Joseph D, Bernie Devlin, Gerard D. Schellenberg, Hakon Hakonarson
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
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3دورية أكاديمية
المؤلفون: Ravinesh A Kumar, Jyotsna Sudi, Timothy D Babatz, Camille W Brune, Donald Oswald, Mayon Yen, Norma J Nowak, Edwin H Cook, Susan L Christian, William B Dobyns
المساهمون: The Pennsylvania State University CiteSeerX Archives
المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/d2/07/J_Med_Genet_2010_Feb_21_47(2)_81-90.tar.gz
وصف الملف: application/zip
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المؤلفون: Lea K. Davis, Nancy J. Cox, James S. Sutcliffe, Camille W. Brune, Emily Kistner-Griffin, Edwin H. Cook
المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 156:139-144
مصطلحات موضوعية: Adult, Adolescent, Genotype, Offspring, Population, Mothers, Article, Genomic Imprinting, Young Adult, Cellular and Molecular Neuroscience, mental disorders, medicine, Humans, Heritability of autism, Allele, Child, education, Alleles, Genetics (clinical), Serotonin transporter, Serotonin Plasma Membrane Transport Proteins, Genetics, education.field_of_study, Polymorphism, Genetic, biology, Maternal effect, medicine.disease, Developmental disorder, Psychiatry and Mental health, Phenotype, Child Development Disorders, Pervasive, Child, Preschool, biology.protein, Autism, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a04878f25c872430fd7a8922b5fe5574Test
https://doi.org/10.1002/ajmg.b.31146Test -
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المؤلفون: Eric Courchesne, Ryan J. Delahanty, James S. Sutcliffe, Jing-Qiong Kang, Nancy J. Cox, Edwin H. Cook, Robert L. Macdonald, Camille W. Brune, Emily O. Kistner
المصدر: Molecular psychiatry
مصطلحات موضوعية: Male, autism, Genome-wide association study, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Childhood absence epilepsy, Gene duplication, mental disorders, GABRB3, medicine, CACNA1H, Humans, Heritability of autism, Copy-number variation, Autistic Disorder, Molecular Biology, Germ-Line Mutation, 030304 developmental biology, Genetics, 0303 health sciences, Chromosomes, Human, Pair 15, biology, GABAA receptor, medicine.disease, Receptors, GABA-A, 3. Good health, Pedigree, Developmental disorder, Psychiatry and Mental health, biology.protein, Autism, epilepsy, Female, imprinting, mutation, Neuroscience, 030217 neurology & neurosurgery, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df52473805f0bd19b31e957740cd8042Test
http://europepmc.org/articles/PMC3428055Test -
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المؤلفون: Joseph Piven, Edward C. Frackelton, Christopher J. McDougle, Patrick M. A. Sleiman, Rosetta M. Chiavacci, John A. Sweeney, Guiqing Cai, Gerard D. Schellenberg, Camille W. Brune, Cuiping Hou, Shana M. Michaels, Rachel M. Game, Wendy Glaberson, Kai Wang, Raphael Bernier, Maja Bucan, Danielle Zurawiecki, Susan E. Levy, Alexander Kolevzon, Hilary Coon, Jeremy M. Silverman, Cecilia E. Kim, Latha Soorya, Nancy J. Minshew, Danielle S. Rudd, David J. Posey, Kacie J. Meyer, James H. Flory, Geraldine Dawson, Emily L. Crawford, Lea K. Davis, Judith Miller, Lambertus Klei, James S. Sutcliffe, Maria Garris, Evdokia Anagnostou, Annette Estes, Marcin Imielinski, Kelly A. Thomas, John I. Nurnberger, Struan F.A. Grant, Thomas H. Wassink, Hakon Hakonarson, Jonathan P. Bradfield, Edwin H. Cook, Bernie Devlin, Frederick G. Otieno, Joseph D. Buxbaum, Shawn Wood, Takeshi Sakurai, Robert T. Schultz, Jeffrey Munson, Thomas Owley, Kiran Annaiah, Joseph T. Glessner, Jennifer Reichert, Haitao Zhang, William M. McMahon, Olena Korvatska
المصدر: Nature. 459:569-573
مصطلحات موضوعية: Genotype, Cell Adhesion Molecules, Neuronal, Gene Dosage, Epigenetics of autism, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Article, Cohort Studies, mental disorders, Genetic variation, medicine, Pervasive developmental disorder, Humans, Gene Regulatory Networks, Genetic Predisposition to Disease, Heritability of autism, Copy-number variation, Autistic Disorder, Neurons, Genetics, Multidisciplinary, Genome, Human, Ubiquitin, Genetic Variation, Reproducibility of Results, medicine.disease, Human genetics, Europe, Developmental disorder, Case-Control Studies, Autism
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::843b651f351c30057edfc7d02605efdbTest
https://doi.org/10.1038/nature07953Test -
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المؤلفون: Susan L. Christian, Jeffrey M. Conroy, Jyotsna Sudi, Edwin H. Cook, Eli Hatchwell, T. Conrad Gilliam, Samer KaraMohamed, Devin McQuaid, Shaung Liu, Camille W. Brune, Judith A. Badner, Sei-Ichi Matsui, Ravinesh A. Kumar, James Gergel, Elliot S. Gershon, William B. Dobyns, Norma J. Nowak
المصدر: Biological Psychiatry. 63:1111-1117
مصطلحات موضوعية: Male, Chromosomes, Artificial, Bacterial, Candidate gene, Genotype, genetic structures, DNA Mutational Analysis, Gene Dosage, Black People, Biology, Polymerase Chain Reaction, Gene dosage, Article, White People, Gene Duplication, Gene duplication, medicine, Humans, Genetic Predisposition to Disease, Copy-number variation, Autistic Disorder, Child, Alleles, Biological Psychiatry, Oligonucleotide Array Sequence Analysis, Chromosome Aberrations, Genetics, Chromosomes, Human, Pair 15, medicine.diagnostic_test, Genetic Variation, Nucleic Acid Hybridization, medicine.disease, Developmental disorder, Phenotype, Autism, Female, Chromosome Deletion, Fluorescence in situ hybridization, Comparative genomic hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93a22c86ca64fe8c8d4718035cd079b2Test
https://doi.org/10.1016/j.biopsych.2008.01.009Test -
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المؤلفون: Jyotsna Sudi, William B. Dobyns, Samer KaraMohamed, Norma J. Nowak, Donald F. Conrad, Edwin H. Cook, T. Conrad Gilliam, Ravinesh A. Kumar, Camille W. Brune, Susan L. Christian, Judith A. Badner
المصدر: Human Molecular Genetics. 17:628-638
مصطلحات موضوعية: Male, Chromosomes, Artificial, Bacterial, Biology, Polymerase Chain Reaction, Neurodevelopmental disorder, Gene Frequency, Genetics, medicine, Humans, Genetic Predisposition to Disease, Heritability of autism, Autistic Disorder, Child, Molecular Biology, In Situ Hybridization, Fluorescence, Genetics (clinical), DNA Primers, Segmental duplication, Base Sequence, medicine.diagnostic_test, Breakpoint, Chromosome Breakage, General Medicine, medicine.disease, Pedigree, Developmental disorder, Phenotype, Case-Control Studies, Autism, Female, Chromosome Deletion, Chromosomes, Human, Pair 16, Microsatellite Repeats, Fluorescence in situ hybridization, Comparative genomic hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecb4d6fa92934846e1a84a2e3f53eedfTest
https://doi.org/10.1093/hmg/ddm376Test -
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المؤلفون: Camille W. Brune, Amanda L. Woodward
المصدر: Journal of Cognition and Development. 8:133-158
مصطلحات موضوعية: Joint attention, Visual perception, genetic structures, Eye movement, Experimental and Cognitive Psychology, Child development, Gaze, Developmental psychology, Psychiatry and Mental health, Interpersonal relationship, Social cognition, Developmental and Educational Psychology, Habituation, Psychology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::948a67ea050b04dd2ad553fff44d9607Test
https://doi.org/10.1080/15248370701202331Test -
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المؤلفون: Catherine Lord, Edwin H. Cook, Soo Jeong Kim, Judith A. Badner, Katherine Ernstrom, Camille W. Brune, Bennett L. Leventhal, Eric Courchesne, Suma Jacob
مصطلحات موضوعية: Proband, Amino Acid Transport System X-AG, Single-nucleotide polymorphism, Biology, behavioral disciplines and activities, Polymorphism, Single Nucleotide, Article, Autism Diagnostic Observation Schedule, mental disorders, Genetics, medicine, SNP, Humans, Family, Genetic Predisposition to Disease, Autistic Disorder, Biological Psychiatry, Genetics (clinical), Genetic Association Studies, SLC1A1, medicine.disease, SNP genotyping, Psychiatry and Mental health, Autism spectrum disorder, biology.protein, Autism
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4d7821f4e74d85cff98e32857f68eb6Test
https://europepmc.org/articles/PMC3210568Test/