Canlyniadau Chwilio - Michael L. Cuccaro
- Dangos 1 - 20 canlyniadau o 50
- Ewch i'r Dudalen Nesaf
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Derivation of autism spectrum disorder-specific induced pluripotent stem cells from peripheral blood mononuclear cells gan Brooke A. DeRosa, Jessica M. Van Baaren, Gaurav Dubey, Joycelyn M. Lee, Michael L. Cuccaro, Jeffery M. Vance, Margaret A. Pericak‐Vance, Derek M. Dykxhoorn
Cyhoeddwyd 2012Artigo -
3
<i>SORL1</i> mutations in early- and late-onset Alzheimer disease gan Michael L. Cuccaro, Regina M. Carney, Yalun Zhang, Christopher Böhm, Brian W. Kunkle, Badri N. Vardarajan, Patrice L. Whitehead, Holly N. Cukier, Richard Mayeux, Peter St George‐Hyslop, Margaret A. Pericak‐Vance
Cyhoeddwyd 2016Artigo -
4
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups gan Ann L. Collins, Deqiong Ma, Patrice L. Whitehead, Eden R. Martin, Harry H. Wright, Ruth K. Abramson, John P. Hussman, Jonathan L. Haines, Michael L. Cuccaro, John R. Gilbert, Margaret A. Pericak‐Vance
Cyhoeddwyd 2006Artigo -
5
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals gan Holly N. Cukier, Raquel Rabionet, Ioanna Konidari, Melissa Y. Rayner‐Evans, Mary L. Baltos, Harry H. Wright, Ruth K. Abramson, Eden R. Martin, Michael L. Cuccaro, Margaret A. Pericak‐Vance, John R. Gilbert
Cyhoeddwyd 2009Artigo -
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Phenotypic Homogeneity Provides Increased Support for Linkage on Chromosome 2 in Autistic Disorder gan Yujun Shao, Kimberly L. Raiford, Chantelle M. Wolpert, Heidi Cope, Sarah A. Ravan, Allison E. Ashley‐Koch, Ruth K. Abramson, Harry H. Wright, Robert DeLong, John R. Gilbert, Michael L. Cuccaro, Margaret A. Pericak‐Vance
Cyhoeddwyd 2002Artigo -
7
Dementia, cognitive impairment in Nigerians aged 90 years or older: A 20-year follow up of survivors of Ibadan study of aging cohort gan Olusegun Baiyewu, Olufisayo Elugbadebo, Sujuan Gao, Michael L. Cuccaro, Jeffery M. Vance, Temitope Farombi, Kathleen A. Lane, Pedro Mena, Farid Rajabil, Rufus Akinyemi, Adesola Ogunniyi, Akin Ojagbemi, Agboola Jamiu Adigun, Hugh C. Hendrie, Margaret A. Pericak‐Vance
Cyhoeddwyd 2025Artigo -
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Multiple rare SAPAP3 missense variants in trichotillomania and OCD gan Stephan Züchner, Jens R. Wendland, Allison E. Ashley‐Koch, Amanda Collins, Khanh-Nhat Tran-Viet, Kaia S. Quinn, Kiara R. Timpano, Michael L. Cuccaro, Margaret A. Pericak‐Vance, David C. Steffens, K. Ranga Krishnan, Guoping Feng, Dennis L. Murphy
Cyhoeddwyd 2008Revisão -
9
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism gan John P. Hussman, Ren-Hua Chung, Anthony J. Griswold, James Jaworski, Daria Salyakina, Deqiong Ma, Ioanna Konidari, Patrice L. Whitehead, Jeffery M. Vance, Eden R. Martin, Michael L. Cuccaro, John R. Gilbert, Jonathan L. Haines, Margaret A. Pericak‐Vance
Cyhoeddwyd 2011Artigo -
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Methylation Clocks Do Not Predict Age or Alzheimer’s Disease Risk Across Genetically Admixed Individuals gan Sebastián Cruz-González, Esther Gu, Lissette Gomez, Makaela Mews, Jeffery M. Vance, Michael L. Cuccaro, Mario Cornejo‐Olivas, Briseida E. Feliciano‐Astacio, Goldie S. Byrd, Jonathan L. Haines, Margaret A. Pericak‐Vance, Anthony J. Griswold, William S. Bush, John A. Capra
Cyhoeddwyd 2025Pré-impressão -
11
Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes gan Yujun Shao, Michael L. Cuccaro, Elizabeth R. Hauser, Kimberly L. Raiford, Marisa M. Menold, Chantelle M. Wolpert, S. A. Ravan, Leigh A. Elston, K. Decena, S. L. Donnelly, Ruth K. Abramson, H Wright, G. R. DeLong, John R. Gilbert, Margaret A Pericak‐Vance
Cyhoeddwyd 2003Artigo -
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Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism gan D.Q. Ma, Patrice L. Whitehead, Marisa M. Menold, Eden R. Martin, Allison E. Ashley‐Koch, Hao Mei, Marylyn D. Ritchie, G. R. DeLong, Ruth K. Abramson, H Wright, Michael L. Cuccaro, John P. Hussman, John R. Gilbert, Margaret A Pericak‐Vance
Cyhoeddwyd 2005Artigo -
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Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons gan Brooke A. DeRosa, Jimmy El Hokayem, Elena Artimovich, Catherine Garcia‐Serje, André W. Phillips, Derek Van Booven, Jonathan E. Nestor, Lily Wang, Michael L. Cuccaro, Jeffery M. Vance, Margaret A. Pericak‐Vance, Holly N. Cukier, Michael W. Nestor, Derek M. Dykxhoorn
Cyhoeddwyd 2018Artigo -
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The Expanding Role of <scp>MBD</scp> Genes in Autism: Identification of a <i><scp>MECP2</scp></i> Duplication and Novel Alterations in <i><scp>MBD5</scp></i>, <i><scp>MBD6</scp></i... gan Holly N. Cukier, Joycelyn M. Lee, Deqiong Ma, Juan I. Young, Vera Mayo, Brittany Butler, Sandhya S. Ramsook, Joseph A. Rantus, Alexander J. Abrams, Patrice L. Whitehead, Harry H. Wright, Ruth K. Abramson, Jonathan L. Haines, Michael L. Cuccaro, Margaret A. Pericak‐Vance, John R. Gilbert
Cyhoeddwyd 2012Artigo -
15
Analysis of the RELN gene as a genetic risk factor for autism gan David Skaar, Yujun Shao, J.L. Haines, Judith E. Stenger, James Jaworski, Eden R. Martin, G. R. DeLong, Jason H. Moore, Jacob L. McCauley, James S. Sutcliffe, Allison E. Ashley‐Koch, Michael L. Cuccaro, Susan E. Folstein, John R. Gilbert, Margaret A. Pericak‐Vance
Cyhoeddwyd 2004Artigo -
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Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk gan Daria Salyakina, Holly N. Cukier, Joycelyn M. Lee, Stephanie Sacharow, Laura Nations, Deqiong Ma, James Jaworski, Ioanna Konidari, Patrice L. Whitehead, Harry H. Wright, Ruth K. Abramson, Scott M. Williams, Ramkumar Menon, Jonathan L. Haines, John R. Gilbert, Michael L. Cuccaro, Margaret A. Pericak‐Vance
Cyhoeddwyd 2011Artigo -
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Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants gan Anthony J. Griswold, Nicole Dueker, Derek Van Booven, Joseph A. Rantus, James Jaworski, Susan H. Slifer, Michael A. Schmidt, William Hulme, Ioanna Konidari, Patrice L. Whitehead, Michael L. Cuccaro, Eden R. Martin, Jonathan L. Haines, John R. Gilbert, John P. Hussman, Margaret A. Pericak‐Vance
Cyhoeddwyd 2015Artigo -
18
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis gan Robert A. Kozol, Holly N. Cukier, Bing Zou, Vera Mayo, Silvia De Rubeis, Guiqing Cai, Anthony J. Griswold, Patrice L. Whitehead, Jonathan L. Haines, John R. Gilbert, Michael L. Cuccaro, Eden R. Martin, James D. Baker, Joseph D. Buxbaum, Margaret A. Pericak‐Vance, Julia E. Dallman
Cyhoeddwyd 2015Artigo -
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Genomic and epigenetic evidence for oxytocin receptor deficiency in autism gan Simon G. Gregory, Jessica J. Connelly, Aaron J. Towers, Jessica Johnson, Dhani Biscocho, Christina A. Markunas, Carla Lintas, Ruth K. Abramson, Harry H. Wright, Peter Ellis, Cordelia F. Langford, Gordon Worley, G. Robert DeLong, Susan K. Murphy, Michael L. Cuccaro, Antonio M. Persico, Margaret A. Pericak‐Vance
Cyhoeddwyd 2009Artigo -
20
Segregation of a rare <i>TTC3</i> variant in an extended family with late-onset Alzheimer disease gan Martin Kohli, Holly N. Cukier, Kara L. Hamilton‐Nelson, Sophie Rolati, Brian W. Kunkle, Patrice L. Whitehead, Stephan Züchner, Lindsay A. Farrer, Eden R. Martin, Gary W. Beecham, Jonathan L. Haines, Jeffery M. Vance, Michael L. Cuccaro, John R. Gilbert, Gerard D. Schellenberg, Regina M. Carney, Margaret A. Pericak‐Vance
Cyhoeddwyd 2016Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Genetics
Gene
Medicine
Autism
Psychiatry
Genotype
Phenotype
Psychology
Single-nucleotide polymorphism
Genome
Genome-wide association study
Internal medicine
Disease
Copy-number variation
Autism spectrum disorder
Heritability of autism
Neuroscience
Population
Developmental psychology
Exome sequencing
Genetic association
Mutation
Candidate gene
Exome
Sociology
Allele
Alzheimer's disease
Apolipoprotein E
Demography