Результаты поиска - Matthew Hill
- Отображение 1 - 16 результаты of 16
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The multiplex model of the genetics of Alzheimer’s disease по Rebecca Sims, Matthew Hill, Julie Williams
Опубликовано 2020Revisão -
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The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability по Marc P. Forrest, Matthew Hill, David H. Kavanagh, Katherine E. Tansey, Adrian J. Waite, Derek J. Blake
Опубликовано 2017Artigo -
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Development of Strategies for SNP Detection in RNA-Seq Data: Application to Lymphoblastoid Cell Lines and Evaluation Using 1000 Genomes Data по Emma M. Quinn, Paul Cormican, Elaine Kenny, Matthew Hill, Richard Anney, Michael Gill, Aiden Corvin, Derek W. Morris
Опубликовано 2013Artigo -
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Mutant Best1 Expression and Impaired Phagocytosis in an iPSC Model of Autosomal Recessive Bestrophinopathy по Alan D. Marmorstein, Adiv A. Johnson, Lori A. Bachman, Cynthia Andrews‐Pfannkoch, Travis Knudsen, Benjamin Gilles, Matthew Hill, Jarel K. Gandhi, Lihua Y. Marmorstein, José S. Pulido
Опубликовано 2018Artigo -
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Psychosis Risk Candidate ZNF804A Localizes to Synapses and Regulates Neurite Formation and Dendritic Spine Structure по P.J. Michael Deans, Pooja Raval, Katherine J. Sellers, Nicholas J. F. Gatford, Sanjay Halai, Rodrigo R. R. Duarte, Carole Shum, Katherine Warre‐Cornish, Victoria E. Kaplun, Graham Cocks, Matthew Hill, Nicholas J. Bray, Jack Price, Deepak P. Srivastava
Опубликовано 2016Artigo -
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Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders по Heath O’Brien, Eilís Hannon, Matthew Hill, Carolina Toste, Matthew J. Robertson, Joanne Morgan, Gemma M. McLaughlin, Cathryn M. Lewis, Leonard C. Schalkwyk, Lynsey S. Hall, Antonio F. Pardiñas, Michael J. Owen, Michael O’Donovan, Jonathan Mill, Nicholas J. Bray
Опубликовано 2018Artigo -
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What does heritability of Alzheimer’s disease represent? по Emily Baker, Ganna Leonenko, Karl Michael Schmidt, Matthew Hill, Amanda Myers, Maryam Shoai, Itziar de Rojas, Niccoló Tesi, Henne Holstege, Wiesje M. van der Flier, Yolande A.L. Pijnenburg, Agustı́n Ruiz, John Hardy, Sven J. van der Lee, Valentina Escott‐Price
Опубликовано 2023Artigo -
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SB‐656104‐A, a novel selective 5‐HT<sub>7</sub> receptor antagonist, modulates REM sleep in rats по David R. Thomas, Sergio Melotto, Mario Massagrande, Andrew D. Gribble, Philip D. Jeffrey, Alexander J. Stevens, Nigel Deeks, Peter Eddershaw, Susan H Fenwick, Graham J. Riley, Tania O. Stean, Claire M. Scott, Matthew Hill, Derek N. Middlemiss, Jim J. Hagan, Gary Price, Ian T. Forbes
Опубликовано 2003Artigo -
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Novel Microtubule-Targeting 7-Deazahypoxanthines Derived from Marine Alkaloid Rigidins with Potent in Vitro and in Vivo Anticancer Activities по Medellin, Derek C., Zhou, Qiong, Scott, Robert, Matthew Hill, R., Frail, Sarah K., Dasari, Ramesh, Ontiveros, Steven J., Pelly, Stephen C., van Otterlo, Willem A. L., Betancourt, Tania, Shuster, Charles B., Hamel, Ernest, Bai, Ruoli, LaBarbera, Daniel V., Rogelj, Snezna, Frolova, Liliya V., Kornienko, Alexander
Опубликовано 2015Текст -
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MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls по Donna Cosgrove, Denise Harold, Omar Mothersill, Richard Anney, Matthew Hill, Nicholas J. Bray, Gabriëlla A.M. Blokland, Tracey L. Petryshen, Peter Donnelly, Lesley Bates, Inês Barroso, Jenefer M. Blackwell, Elvira Bramon, Matthew A. Brown, Juan P. Casas, Aiden Corvin, Panos Deloukas, Audrey Duncanson, Janusz Jankowski, Hugh S. Markus, Christopher G. Mathew, Colin N. A. Palmer, Robert Plomin, Anna Rautanen, Stephen Sawcer, Richard C. Trembath, Ananth C. Viswanathan, Nicholas Wood, Chris C. A. Spencer, Gavin Band, Céline Bellenguez, Colin Freeman, Garrett Hellenthal, Eleni Giannoulatou, Lucinda Hopkins, Matti Pirinen, Richard D. Pearson, Amy Strange, Zhan Su, Damjan Vukcevic, Cordelia Langford, Sarah Hunt, Sarah Edkins, Rhian Gwilliam, Hannah Blackburn, Suzannah J. Bumpstead, Serge Dronov, Matthew W. Gillman, Emma Gray, Naomi Hammond, Alagurevathi Jayakumar, Owen T McCann, Jennifer Liddle, Simon Potter, Rathi Ravindrarajah, Michelle Ricketts, Matthew Waller, PaulWeston Weston, SaraWidaa Widaa, Pamela Whittaker, Alexander Richards, Kiran K. Mantripragada, Michael J. Owen, Michael O’Donovan, Michael Gill, Aiden Corvin, Derek W. Morris, Gary Donohoe
Опубликовано 2017Artigo -
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Functional impact of global rare copy number variation in autism spectrum disorders по Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R. Magalhães, Catarina Correia, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Gary D. Bader, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Sven Bölte, Patrick Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, Susan E. Bryson, Andrew R. Carson, Guillermo Casallo, Jillian P. Casey, Brian Hon‐Yin Chung, Lynne Cochrane, Christina Corsello, Emily L. Crawford, Andrew Crossett, Cheryl Cytrynbaum, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Hákon Hákonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Anath C. Lionel, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge
Опубликовано 2010Artigo -
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A genome-wide scan for common alleles affecting risk for autism по Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Jennifer Conroy, Tiago R. Magalhães, Catarina Correia, Brett S. Abrahams, N. Sykes, A. T. Pagnamenta, J.-P. de Almeida, Elena Bacchelli, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Sven Bölte, P. F. Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, A. R. Carson, Guillermo Casallo, Jillian P. Casey, Su H. Chu, Lynne Cochrane, Christina Corsello, E. L. Crawford, A. Crossett, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, James Gilbert, Christopher Gillberg, Joseph Glessner, Joel O. Goldberg, Jonathan Green, Stephen J. Guter, Hákon Hákonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, C. Kim, Sabine M. Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, A. C. Lionel, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Nadine Melhem, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, C. Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Joseph Piven, David J. Posey, Annemarie Poustka, Fritz Poustka
Опубликовано 2010Artigo
Инструменты поиска:
Связанные темы
Biology
Genetics
Gene
Genotype
Medicine
Single-nucleotide polymorphism
Genetic association
Genome-wide association study
Psychiatry
Psychology
Autism
Gene expression
Neuroscience
Computational biology
Genome
Missing heritability problem
SNP
Allele
Cell
Cell biology
Clinical psychology
Cognition
Expression quantitative trait loci
Gene expression profiling
Heritability
Human genome
In vitro
Neurite
Phenotype
Psychosis