检索结果 - M. E. Suzanne Lewis
- Showing 1 - 20 results of 31
- Go to Next Page
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
-
10
-
11
DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair fa... 由 Joe A. Hettinger, Xudong Liu, Melissa L. Hudson, Alana Lee, Ira L. Cohen, Ron C. Michaelis, Charles E. Schwartz, M. E. Suzanne Lewis, Jeanette JA Holden
出版 2012Artigo -
12
-
13
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1 由 Evica Rajcan‐Separovic, Chansonette Harvard, X Liu, Barbara McGillivray, Judith G. Hall, Ying Qiao, Jane Hurlburt, Joanna Hildebrand, Elizabeth C. R. Mickelson, J.J.A. Holden, M. E. Suzanne Lewis
出版 2006Carta -
14
Correlates of age at diagnosis of autism spectrum disorders in six Canadian regions 由 Helen Coo, Hélène Ouellette‐Kuntz, Miu Lam, C. T. Yu, Deborah Dewey, François Bernier, Albert E. Chudley, P.E. Hennessey, M. Breitenbach, Andrea Noonan, M. E. Suzanne Lewis, Jeanette J. A. Holden
出版 2012Artigo -
15
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG) 由 Melissa T. Carter, Myriam Srour, Ping-Yee Billie Au, Daniela Buhaş, Sarah Dyack, Alison Eaton, Michal Inbar‐Feigenberg, Heather Howley, Anne Kawamura, M. E. Suzanne Lewis, M. Elizabeth McCready, Tanya N. Nelson, Hilary Vallance
出版 2023Artigo -
16
Weaver Syndrome‐Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In Vitro 由 Ana S.A. Cohen, Damian Yap, M. E. Suzanne Lewis, Chieko Chijiwa, María A. Ramos‐Arroyo, Natália Tkachenko, Valentina Milano, Mélanie Fradin, Margaret L. McKinnon, Katelin N. Townsend, Jieqing Xu, M. I. Van Allen, Colin J.D. Ross, William B. Dobyns, David D. Weaver, William T. Gibson
出版 2015Artigo -
17
Understanding the impact of 1q21.1 copy number variant 由 Chansonette Harvard, Emma Strong, Eloi Mercier, Rita Colnaghi, Diana Alcantara, Eva W. C. Chow, Sally Martell, Christine Tyson, Monica Hrynchak, Barbara McGillivray, Sara Hamilton, Sandra L. Marles, Aziz Mhanni, Angelika J. Dawson, Paul Pavlidis, Ying Qiao, J.J.A. Holden, M. E. Suzanne Lewis, Mark O’Driscoll, Evica Rajcan‐Separovic
出版 2011Artigo -
18
Genome Plasticity of <i>agr</i> -Defective Staphylococcus aureus during Clinical Infection 由 Deena R. Altman, Mitchell J. Sullivan, Kieran Chacko, Divya Balasubramanian, Theodore R. Pak, William E. Sause, Krishan Kumar, Robert Sebra, Gintaras Deikus, Oliver Attie, Hannah R. Rose, M. E. Suzanne Lewis, Yi Fulmer, Ali Bashir, Andrew Kasarskis, Eric E. Schadt, Anthony R. Richardson, Victor J. Torres, Bo Shopsin, Harm van Bakel
出版 2018Artigo -
19
A genome-wide DNA methylation signature for SETD1B-related syndrome 由 I. Krzyzewska, Saskia M. Maas, Peter Henneman, K. Lip, A. Venema, Kristin Barañano, Anna Chassevent, Erfan Aref‐Eshghi, Anthonie J. van Essen, Tokiko Fukuda, Hiroko Ikeda, M. Jacquemont, H.-G. Kim, Audrey Labalme, M. E. Suzanne Lewis, Gaëtan Lesca, Irene Madrigal, Sonal Mahida, Naomichi Matsumoto, Raquel Rabionet, Evica Rajcan‐Separovic, Ying Qiao, Bekim Sadiković, Hirotomo Saitsu, David A. Sweetser, Mariëlle Alders, Marcel M.A.M. Mannens
出版 2019Artigo -
20
Genome-wide detection of tandem DNA repeats that are expanded in autism 由 Brett Trost, Worrawat Engchuan, Charlotte Nguyen, Bhooma Thiruvahindrapuram, Egor Dolzhenko, Ian Backstrom, Mila Mirceta, Bahareh A. Mojarad, Yue Yin, Alona Dov, Induja Chandrakumar, Tanya Prasolava, Natalie Shum, Omar Hamdan, Giovanna Pellecchia, Jennifer Howe, Joseph Whitney, Eric W. Klee, Saurabh Baheti, David G. Amaral, Evdokia Anagnostou, Mayada Elsabbagh, Bridget A. Fernandez, Ny Hoang, M. E. Suzanne Lewis, Xudong Liu, Calvin Sjaarda, Isabel M. Smith, Peter Szatmari, Lonnie Zwaigenbaum, David Glazer, Dean M. Hartley, A. Keith Stewart, Michael A. Eberle, Nozomu Sato, Christopher E. Pearson, Stephen W. Scherer, Ryan K. C. Yuen
出版 2020Artigo
相关主题
Biology
Gene
Genetics
Medicine
Psychiatry
Autism
Genome
Phenotype
Psychology
Autism spectrum disorder
Computational biology
Gene expression
Intellectual disability
Internal medicine
Mutation
Population
DNA methylation
Epigenetics
Genotype
Allele
Bioinformatics
Chromatin
Computer science
Copy-number variation
Demography
Disease
Endocrinology
Environmental health
Law
Methylation