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by Koboldt, Daniel C and Fulton, Robert S and McLellan, Michael D and Schmidt, Heather and Kalicki-Veizer, Joelle and McMichael, Joshua F and Fulton, Lucinda L and Dooling, David J and Ding, Li and Mardis, Elaine R and Wilson, Richard K and Ally, Adrian and Balasundaram, Miruna and Butterfield, Yaron S. N and Carlsen, Rebecca and Carter, Candace and Chu, Andy and Chuah, Eric and Chun, Hye-Jung E and Coope, Robin J. N and Dhalla, Noreen and Guin, Ranabir and Hirst, Carrie and Hirst, Martin and Holt, Robert A and Lee, Darlene and Li, Haiyan I and Mayo, Michael and Moore, Richard A and Mungall, Andrew J and Pleasance, Erin and Robertson, A. Gordon and Schein, Jacqueline E and Shafiei, Arash and Sipahimalani, Payal and Slobodan, Jared R and Stoll, Dominik and Tam, Angela and Thiessen, Nina and Varhol, Richard J and Wye, Natasja and Zeng, Thomas and Zhao, Yongjun and Birol, Inanc and Jones, Steven J. M and Marra, Marco A and Cherniack, Andrew D and Saksena, Gordon and Onofrio, Robert C and Pho, Nam H and Carter, Scott L and Schumacher, Steven E and Tabak, Barbara and Hernandez, Bryan and Gentry, Jeff and Nguyen, Huy and Crenshaw, Andrew and Ardlie, Kristin and Beroukhim, Rameen and Winckler, Wendy and Getz, Gad and Gabriel, Stacey B and Meyerson, Matthew and Chin, Lynda and Kucherlapati, Raju and Hoadley, Katherine A and Auman, J. Todd and Fan, Cheng and Turman, Yidi J and Shi, Yan and Li, Ling and Topal, Michael D and He, Xiaping and Chao, Hann-Hsiang and Prat, Aleix and Silva, Grace O and Iglesia, Michael D and Zhao, Wei and Usary, Jerry and Berg, Jonathan S and Adams, Michael and Booker, Jessica and Wu, Junyuan and Gulabani, Anisha and Bodenheimer, Tom and Hoyle, Alan P and Simons, Janae V and Soloway, Matthew G and Mose, Lisle E and Jefferys, Stuart R and Balu, Saianand and Parker, Joel S and Hayes, D. Neil and Perou, Charles M and Malik, Simeen and Mahurkar, Swapna and Shen, Hui and Weisenberger, Daniel J and Triche Jr, Timothy and Lai, Phillip H and ... and Canc Genome Atlas Network and Cancer Genome Atlas Network and The Cancer Genome Atlas Network
Nature, ISSN 0028-0836, 10/2012, Volume 490, Issue 7418, pp. 61 - 70
We analysed primary breast cancers by genomic DNA copy number arrays, DNA methylation, exome sequencing, messenger RNA arrays, microRNA sequencing and... 
PATHWAYS | TARGET | BASAL-LIKE | SUPPRESSOR | PIK3CA GENE | SUBTYPES | MULTIDISCIPLINARY SCIENCES | HIGH-FREQUENCY | LUMINAL-B | CANCER | MUTATIONAL EVOLUTION | GATA3 Transcription Factor - genetics | Receptors, Estrogen - metabolism | Oligonucleotide Array Sequence Analysis | Genomics | Humans | Gene Expression Regulation, Neoplastic | Ovarian Neoplasms - pathology | Gene Expression Profiling | Breast Neoplasms - metabolism | Ovarian Neoplasms - genetics | DNA Methylation | DNA Mutational Analysis | Female | Genes, BRCA1 | Genes, Neoplasm - genetics | Breast Neoplasms - classification | RNA, Messenger - genetics | Retinoblastoma Protein - metabolism | DNA Copy Number Variations - genetics | Genes, p53 - genetics | Mutation - genetics | Genetic Heterogeneity | Genome, Human - genetics | Phosphatidylinositol 3-Kinases - genetics | Exome - genetics | Breast Neoplasms - genetics | Class I Phosphatidylinositol 3-Kinases | Breast Neoplasms - pathology | Retinoblastoma Protein - genetics | Genes, erbB-2 - genetics | Proteomics | Protein Array Analysis | RNA, Neoplasm - genetics | MAP Kinase Kinase Kinase 1 - genetics | MicroRNAs - genetics | Breast tumors | Gene mutations | Oncology, Experimental | Genetic aspects | Research | Identification and classification | Cancer | Proteins | DNA methylation | Genetics | Breast cancer | Mutation | Index Medicus | Càncer de mama | Oncologia | Oncology | Gene expression | Expressió gènica | Genòmica
Journal Article
by Feliciano, Pamela and Daniels, Amy M and Green Snyder, LeeAnne and Beaumont, Amy and Camba, Alexies and Esler, Amy and Gulsrud, Amanda G and Mason, Andrew and Gutierrez, Anibal and Nicholson, Amy and Paolicelli, Anna Marie and McKenzie, Alexander P and Rachubinski, Angela L and Stephens, Alexandra N and Simon, Laura and Simon, Andrea R and Stedman, Amy and Shocklee, Amanda D and Swanson, Amy and Finucane, Brenda and Hilscher, Brittani A and Hauf, Brenda and O’Roak, Brian J and McKenna, Brooke and Robertson, Beverly E and Rodriguez, Barbara and Vernoia, Brianna M and Van Metre, Bonnie and Bradley, Catherine and Cohen, Cheryl and Erickson, Craig A and Harkins, Christina and Hayes, Caitlin and Lord, Catherine and Martin, Christa Lese and Ortiz, Crissy and Ochoa-Lubinoff, Cesar and Peura, Christine and Rice, Catherine E and Rosenberg, Cordelia R and Smith, Christopher J and Smith, Kaitlin and Thomas, Carrie and Taylor, Cora M and White, Loran Casey and White, Sabrina and Walston, Corrie H and Amaral, David G and Coury, Daniel Lee and Sarver, Dustin E and Istephanous, Dalia and Li, Deana and Li, Hai and Nugyen, Dzung Cong and Fox, Emily A and Butter, Eric M and Berry-Kravis, Elizabeth and Courchesne, Eric and Fombonne, Eric J and Hofammann, Eugenia and Lamarche, Elena and Wodka, Ericka L and Matthews, Emily T and O’Connor, Eirene and Palen, Emily and Miller, Fiona and Dichter, Gabriel S and Marzano, Gabriela and Stein, Gail and Hutter, Hanna and Kaplan, Hannah E and Lechniak, Holly and Schneider, Hoa Lam and Zaydens, Hana and Arriaga, Ivette and Gerdts, Jennifer A and Cubells, Joseph F and Cordova, Jeanette M and Gunderson, Jaclyn and Lillard, Joseph and Manoharan, Julie and McCracken, James T and Michaelson, Jacob J and Neely, Jason and Orobio, Jessica and Pandey, Juhi and Piven, Joseph and Scherr, Jessica and Sutcliffe, James S and Tjernagel, Jennifer and Wallace, Jermel and Callahan, Kristen and Dent, Katherine and Schweers, Kathryn A and Hamer, Kira E and Law, J. Kiely and Lowe, Kathryn and O’Brien, Kaela and Pawlowski, Katherine G and Pierce, Karen L and ... and SPARK Consortium and SPARK Consortium. Electronic address: pfeliciano@simonsfoundation.org
Neuron, ISSN 0896-6273, 02/2018, Volume 97, Issue 3, pp. 488 - 493
The Simons Foundation Autism Research Initiative (SFARI) has launched , a dynamic platform that is engaging thousands of individuals with autism spectrum... 
RISK | NEUROSCIENCES | SPECTRUM DISORDER | DISEASE | Autism | Family | Congenital diseases | Working groups | Genomics | Genes | Families & family life | Systematic review | Genomes | Research | Environmental risk | Meta-analysis | Studies | Consortia | Researchers | Mutation | Pollutants
Journal Article
Science, ISSN 0036-8075, 4/2011, Volume 332, Issue 6029, pp. 604 - 607
Journal Article
International Journal of Palliative Nursing, ISSN 1357-6321, 03/2018, Volume 24, Issue 3, pp. 132 - 144
Advance care planning (ACP) engagement and completion of advance directives remain low in patients undergoing haematopoietic stem cell transplantation, despite... 
Qualitative research | Palliative care | Advance care planning | Haematopoietic stem cell transplantation
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 03/2019, Volume 24, Issue 3, pp. 338 - 344
Fragile X syndrome is rare but a prominent cause of intellectual disability. It is usually caused by a de novo mutation that occurs on multiple haplotypes and... 
INSTABILITY | PROTEIN | PSYCHIATRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | LENGTH | RISK | LOCI | NEUROSCIENCES | REGION | GENETIC-VARIATION | CGG REPEAT | EXPANSION | MALES | Gene mutations | Genetic aspects | Research | Fragile X syndrome | Mental retardation | Chromosomes | Risk factors | Haplotypes | Fragile X mental retardation protein | Mapping | Genomes | Mutation | Risk management | Gene mapping | FMR1 protein
Journal Article
JOURNAL OF CLINICAL ONCOLOGY, ISSN 0732-183X, 10/2016, Volume 34, Issue 26, pp. 7 - 7
Conference Proceeding
Cancer Cytopathology, ISSN 1934-662X, 06/2016, Volume 124, Issue 6, pp. 406 - 414
Journal Article