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SYSTEMATIC REVIEW OF HEALTHY EATING INDEXES IN ADULTS AND ELDERLY: APPLICABILITY AND VALIDITY.
Published in:
2015
By:
- de Souza Fernandes, Dalila Pinto;
- Ribeiro, Andréia Queiroz;
- Lopes Duarte, Maria Sônia;
- do Carmo Castro Franceschini, Sylvia;
- Pinto de Souza Fernandes, Dalila;
- Queiroz Ribeiro, Andréia;
- Castro Franceschini, Sylvia do Carmo
Publication type:
journal article
Calf circumference is an independent predictor of mortality in older adults: An approach with generalized additive models.
Published in:
Nutrition in Clinical Practice, 2022, v. 37, n. 5, p. 1190, doi. 10.1002/ncp.10780
By:
- Fernandes, Dalila Pinto de Souza;
- Juvanhol, Leidjaira Lopes;
- Lozano, Manuel;
- Ribeiro, Andréia Queiroz
Publication type:
Article
mTADA is a framework for identifying risk genes from de novo mutations in multiple traits.
Published in:
Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16487-z
By:
- Nguyen, Tan-Hoang;
- Dobbyn, Amanda;
- Brown, Ruth C.;
- Riley, Brien P.;
- Buxbaum, Joseph D.;
- Pinto, Dalila;
- Purcell, Shaun M.;
- Sullivan, Patrick F.;
- He, Xin;
- Stahl, Eli A.
Publication type:
Article
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
Published in:
Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0497-y
By:
- Nguyen, Hoang T.;
- Bryois, Julien;
- Kim, April;
- Dobbyn, Amanda;
- Huckins, Laura M.;
- Munoz-Manchado, Ana B.;
- Ruderfer, Douglas M.;
- Genovese, Giulio;
- Fromer, Menachem;
- Xinyi Xu;
- Pinto, Dalila;
- Linnarsson, Sten;
- Verhage, Matthijs;
- Smit, August B.;
- Hjerling-Leffler, Jens;
- Buxbaum, Joseph D.;
- Hultman, Christina;
- Sklar, Pamela;
- Purcell, Shaun M.;
- Lage, Kasper
Publication type:
Article
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.
Published in:
Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 113, doi. 10.1007/s11689-011-9072-9
By:
- Vieland, Veronica;
- Hallmayer, Joachim;
- Huang, Yungui;
- Pagnamenta, Alistair;
- Pinto, Dalila;
- Khan, Hameed;
- Monaco, Anthony;
- Paterson, Andrew;
- Scherer, Stephen;
- Sutcliffe, James;
- Szatmari, Peter
Publication type:
Article
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.
Published in:
Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 124, doi. 10.1007/s11689-011-9076-5
By:
- Pagnamenta, Alistair;
- Holt, Richard;
- Yusuf, Mohammed;
- Pinto, Dalila;
- Wing, Kirsty;
- Betancur, Catalina;
- Scherer, Stephen;
- Volpi, Emanuela;
- Monaco, Anthony
Publication type:
Article
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
Published in:
PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004580
By:
- Leblond, Claire S.;
- Nava, Caroline;
- Polge, Anne;
- Gauthier, Julie;
- Huguet, Guillaume;
- Lumbroso, Serge;
- Giuliano, Fabienne;
- Stordeur, Coline;
- Depienne, Christel;
- Mouzat, Kevin;
- Pinto, Dalila;
- Howe, Jennifer;
- Lemière, Nathalie;
- Durand, Christelle M.;
- Guibert, Jessica;
- Ey, Elodie;
- Toro, Roberto;
- Peyre, Hugo;
- Mathieu, Alexandre;
- Amsellem, Frédérique
Publication type:
Article
Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism.
Published in:
PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003523
By:
- Noh, Hyun Ji;
- Ponting, Chris P.;
- Boulding, Hannah C.;
- Meader, Stephen;
- Betancur, Catalina;
- Buxbaum, Joseph D.;
- Pinto, Dalila;
- Marshall, Christian R.;
- Lionel, Anath C.;
- Scherer, Stephen W.;
- Webber, Caleb
Publication type:
Article
Explorative two?locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures?related photosensitivity loci.
Published in:
Genetic Epidemiology, 2007, v. 31, n. 1, p. 42, doi. 10.1002/gepi.20190
By:
- Dalila Pinto;
- Dorothée G.A. Kasteleijn?Nolst Trenité;
- Heather J. Cordell;
- Manuel Mattheisen;
- Konstantin Strauch;
- Dick Lindhout;
- Bobby P.C. Koeleman
Publication type:
Article
Functional impact of global rare copy number variation in autism spectrum disorders.
Published in:
Nature, 2010, v. 466, n. 7304, p. 368, doi. 10.1038/nature09146
By:
- Pinto, Dalila;
- Pagnamenta, Alistair T.;
- Klei, Lambertus;
- Anney, Richard;
- Merico, Daniele;
- Regan, Regina;
- Conroy, Judith;
- Magalhaes, Tiago R.;
- Correia, Catarina;
- Abrahams, Brett S.;
- Almeida, Joana;
- Bacchelli, Elena;
- Bader, Gary D.;
- Bailey, Anthony J.;
- Baird, Gillian;
- Battaglia, Agatino;
- Berney, Tom;
- Bolshakova, Nadia;
- Bölte, Sven;
- Bolton, Patrick F.
Publication type:
Article
Origins and functional impact of copy number variation in the human genome.
Published in:
Nature, 2010, v. 464, n. 7289, p. 704, doi. 10.1038/nature08516
By:
- Conrad, Donald F.;
- Pinto, Dalila;
- Redon, Richard;
- Feuk, Lars;
- Gokcumen, Omer;
- Yujun Zhang;
- Aerts, Jan;
- Andrews, T. Daniel;
- Barnes, Chris;
- Campbell, Peter;
- Fitzgerald, Tomas;
- Min Hu;
- Chun Hwa Ihm;
- Kristiansson, Kati;
- MacArthur, Daniel G.;
- MacDonald, Jeffrey R.;
- Onyiah, Ifejinelo;
- Wing Chun Pang, Andy;
- Robson, Sam;
- Stirrups, Kathy
Publication type:
Article
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.
Published in:
Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-28
By:
- Correia, Catarina T.;
- Conceição, Inês C.;
- Oliveira, Bárbara;
- Coelho, Joana;
- Sousa, Inês;
- Sequeira, Ana F.;
- Almeida, Joana;
- Café, Cátia;
- Duque, Frederico;
- Mouga, Susana;
- Roberts, Wendy;
- Kun Gao;
- Lowe, Jennifer K.;
- Thiruvahindrapuram, Bhooma;
- Walker, Susan;
- Marshall, Christian R.;
- Pinto, Dalila;
- Nurnberger, John I.;
- Scherer, Stephen W.;
- Geschwind, Daniel H.
Publication type:
Article
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.
Published in:
Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-34
By:
- Buxbaum, Joseph D.;
- Bolshakova, Nadia;
- Brownfeld, Jessica M.;
- Anney, Richard J. L.;
- Bender, Patrick;
- Bernier, Raphael;
- Cook, Edwin H.;
- Coon, Hilary;
- Cuccaro, Michael;
- Freitag8, Christine M.;
- Hallmayer, Joachim;
- Geschwind, Daniel;
- Klauck, Sabine M.;
- Nurnberger, John I.;
- Oliveira, Guiomar;
- Pinto, Dalila;
- Poustka, Fritz;
- Scherer, Stephen W.;
- Shih, Andy;
- Sutcliffe, James S.
Publication type:
Article
EFFECT OF EICOSAPENTAENOIC ACID AND DOCOSAHEXAENOIC ACID SUPPLEMENTATIONS TO CONTROL COGNITIVE DECLINE IN DEMENTIA AND ALZHEIMER'S DISEASE: A SYSTEMATIC REVIEW.
Published in:
2015
By:
- de Souza Fernandes, Dalila Pinto;
- Canaan Rezende, Fabiane Aparecida;
- Rocha, Gabriele Pereira;
- De Santis Filgueiras, Mariana;
- Silva Moreira, Patrícia Regina;
- de Cássia Gonçalves Alfenas, Rita;
- Pereira Rocha, Gabriele;
- Gonçalves Alfenas, Rita de Cássia
Publication type:
journal article
A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV data.
Published in:
BMC Bioinformatics, 2011, v. 12, n. 1, p. 205, doi. 10.1186/1471-2105-12-205
By:
- Nishiyama, Takeshi;
- Takahashi, Kunihiko;
- Tango, Toshiro;
- Pinto, Dalila;
- Scherer, Stephen W.;
- Takami, Satoshi;
- Kishino, Hirohisa
Publication type:
Article
Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
Published in:
Human Molecular Genetics, 2012, v. 21, n. 21, p. 4781, doi. 10.1093/hmg/dds301
By:
- Anney, Richard;
- Klei, Lambertus;
- Pinto, Dalila;
- Almeida, Joana;
- Bacchelli, Elena;
- Baird, Gillian;
- Bolshakova, Nadia;
- Bölte, Sven;
- Bolton, Patrick F.;
- Bourgeron, Thomas;
- Brennan, Sean;
- Brian, Jessica;
- Casey, Jillian;
- Conroy, Judith;
- Correia, Catarina;
- Corsello, Christina;
- Crawford, Emily L.;
- de Jonge, Maretha;
- Delorme, Richard;
- Duketis, Eftichia
Publication type:
Article
A genome-wide scan for common alleles affecting risk for autism.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 20, p. 4072, doi. 10.1093/hmg/ddq307
By:
- Anney, Richard;
- Klei, Lambertus;
- Pinto, Dalila;
- Regan, Regina;
- Conroy, Judith;
- Magalhaes, Tiago R.;
- Correia, Catarina;
- Abrahams, Brett S.;
- Sykes, Nuala;
- Pagnamenta, Alistair T.;
- Almeida, Joana;
- Bacchelli, Elena;
- Bailey, Anthony J.;
- Baird, Gillian;
- Battaglia, Agatino;
- Berney, Tom;
- Bolshakova, Nadia;
- Bölte, Sven;
- Bolton, Patrick F.;
- Bourgeron, Thomas
Publication type:
Article
Copy-number variation in control population cohorts.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 3, p. 466
By:
- Pinto, Dalila;
- Marshall, Christian;
- Feuk, Lars;
- Scherer, Stephen W.
Publication type:
Article
Copy-number variation in control population cohorts.
Published in:
Human Molecular Genetics, 2007, v. 16, n. R2, p. R168, doi. 10.1093/hmg/ddm241
By:
- Pinto, Dalila;
- Marshall, Christian;
- Feuk, Lars;
- Scherer, Stephen W.
Publication type:
Article
Healthy Eating Index: Assessment of the Diet Quality of a Brazilian Elderly Population.
Published in:
Nutrition & Metabolic Insights, 2018, v. 11, p. 1, doi. 10.1177/1178638818818845
By:
- Fernandes, Dalila Pinto de Souza;
- Lopes Duarte, Maria Sônia;
- Pessoa, Milene Cristine;
- Castro Franceschini, Sylvia do Carmo;
- Queiroz Ribeiro, Andréia
Publication type:
Article
A Deletion Involving CD 38 and BST 1 Results in a Fusion Transcript in a Patient With Autism and Asthma.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 2, p. 254, doi. 10.1002/aur.1365
By:
- Ceroni, Fabiola;
- Sagar, Angela;
- Simpson, Nuala H.;
- Gawthrope, Alex J.T.;
- Newbury, Dianne F.;
- Pinto, Dalila;
- Francis, Sunday M.;
- Tessman, Dorothy C.;
- Cook, Edwin H.;
- Monaco, Anthony P.;
- Maestrini, Elena;
- Pagnamenta, Alistair T.;
- Jacob, Suma
Publication type:
Article
Erratum: A genotype resource for postmortem brain samples from the Autism Tissue Program.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2011, v. 4, n. 4, p. 314, doi. 10.1002/aur.211
By:
- Wintle, Richard F.;
- Lionel, Anath C.;
- Hu, Pingzhao;
- Ginsberg, Stephen D.;
- Pinto, Dalila;
- Thiruvahindrapduram, Bhooma;
- Wei, John;
- Marshall, Christian R.;
- Pickett, Jane;
- Cook, Edwin H.;
- Scherer, Stephen W.
Publication type:
Article
A genotype resource for postmortem brain samples from the Autism Tissue Program.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2011, v. 4, n. 2, p. 89, doi. 10.1002/aur.173
By:
- Wintle, Richard F.;
- Lionel, Anath C.;
- Hu, Pingzhao;
- Ginsberg, Stephen D.;
- Pinto, Dalila;
- Thiruvahindrapduram, Bhooma;
- Wei, John;
- Marshall, Christian R.;
- Pickett, Jane;
- Cook, Edwin H.;
- Scherer, Stephen W.
Publication type:
Article
Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms.
Published in:
PLoS ONE, 2008, v. 3, n. 5, p. 1, doi. 10.1371/journal.pone.0002270
By:
- Monsuur, Alienke J.;
- de Bakker, Paul I. W.;
- Zhernakova, Alexandra;
- Pinto, Dalila;
- Verduijn, Willem;
- Romanos, Jihane;
- Auricchio, Renata;
- Lopez, Ana;
- van Heel, David A.;
- Crusius, J. Bart A.;
- Wijmenga, Cisca
Publication type:
Article
Molecular characteristics of a pancreatic adenocarcinoma associated with Shwachman-Diamond syndrome.
Published in:
Pediatric Blood & Cancer, 2013, v. 60, n. 5, p. 754, doi. 10.1002/pbc.24453
By:
- Dhanraj, Santhosh;
- Manji, Arif;
- Pinto, Dalila;
- Scherer, Stephen W.;
- Favre, Helen;
- Loh, Mignon L.;
- Chetty, Runjan;
- Wei, Alice C.;
- Dror, Yigal
Publication type:
Article
Genome-Wide Analysis of Large Rare Copy Number Variations in Alzheimer Disease Among Caribbean Hispanics
Published in:
2011
By:
- Rogaeva, Ekaterina;
- Ghani, Mahdi;
- Pinto, Dalila;
- Lee, Joseph;
- Reitz, Christiane;
- Scherer, Stephen;
- Mayeux, Richard;
- St. George-Hyslop, Peter
Publication type:
Abstract
Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.
Published in:
Nature Genetics, 2010, v. 42, n. 6, p. 489, doi. 10.1038/ng.589
By:
- Berkel, Simone;
- Marshall, Christian R.;
- Weiss, Birgit;
- Howe, Jennifer;
- Roeth, Ralph;
- Moog, Ute;
- Endris, Volker;
- Roberts, Wendy;
- Szatmari, Peter;
- Pinto, Dalila;
- Bonin, Michael;
- Riess, Angelika;
- Engels, Hartmut;
- Sprengel, Rolf;
- Scherer, Stephen W.;
- Rappold, Gudrun A.
Publication type:
Article
Ações de fotoeducação em saúde no ambiente escolar como estratégia para a prevenção de fotodermatoses.
Published in:
Revista Brasileira de Extensão Universitária, 2020, v. 11, n. 3, p. 397, doi. 10.36661/2358-0399.2020v11i3.11548
By:
- Nagem Lopes, Luis Phillipe;
- Barros Bastos, Agatha Cristiny;
- Fileto Caldeira, Luiz Eduardo;
- Nigro, Fiammetta;
- Faria de Freitas, Zaida Maria;
- Cerqueira Pinto, Dalila dos Santos;
- Barros dos Passos, Márcia Maria;
- Souza Lorca, Bárbara da Silva e;
- Pereira dos Santos, Elisabete
Publication type:
Article
Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13.
Published in:
Human Molecular Genetics, 2005, v. 14, n. 1, p. 171, doi. 10.1093/hmg/ddi018
By:
- Pinto, Dalila;
- Westland, Birgit;
- de Haan, Gerrit-Jan;
- Rudolf, Gabrielle;
- da Silva, Berta Martins;
- Hirsch, Edouard;
- Lindhout, Dick;
- Trenité, Dorothée G.A. Kasteleijn-Nolst;
- Koeleman, Bobby P.C.
Publication type:
Article
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder.
Published in:
Nature Genetics, 2014, v. 46, n. 7, p. 742, doi. 10.1038/ng.2980
By:
- Uddin, Mohammed;
- Tammimies, Kristiina;
- Pellecchia, Giovanna;
- Alipanahi, Babak;
- Hu, Pingzhao;
- Wang, Zhuozhi;
- Pinto, Dalila;
- Lau, Lynette;
- Nalpathamkalam, Thomas;
- Marshall, Christian R;
- Blencowe, Benjamin J;
- Frey, Brendan J;
- Merico, Daniele;
- Yuen, Ryan K C;
- Scherer, Stephen W
Publication type:
Article
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Published in:
Human Mutation, 2015, v. 36, n. 9, p. 842, doi. 10.1002/humu.22816
By:
- Addis, Laura;
- Ahn, Joo Wook;
- Dobson, Richard;
- Dixit, Abhishek;
- Ogilvie, Caroline M;
- Pinto, Dalila;
- Vaags, Andrea K;
- Coon, Hilary;
- Chaste, Pauline;
- Wilson, Scott;
- Parr, Jeremy R;
- Andrieux, Joris;
- Lenne, Bruno;
- Tumer, Zeynep;
- Leuzzi, Vincenzo;
- Aubell, Kristina;
- Koillinen, Hannele;
- Curran, Sarah;
- Marshall, Christian R;
- Scherer, Stephen W
Publication type:
Article
Correction: High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy.
Published in:
2022
By:
- Pai, Balagopal;
- Tome‑Garcia, Jessica;
- Cheng, Wan Sze;
- Nudelman, German;
- Beaumont, Kristin G.;
- Ghatan, Saadi;
- Panov, Fedor;
- Caballero, Elodia;
- Sarpong, Kwadwo;
- Marcuse, Lara;
- Yoo, Jiyeoun;
- Jiang, Yan;
- Schaefer, Anne;
- Akbarian, Schahram;
- Sebra, Robert;
- Pinto, Dalila;
- Zaslavsky, Elena;
- Tsankova, Nadejda M.
Publication type:
Correction Notice
High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy.
Published in:
Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01453-1
By:
- Pai, Balagopal;
- Tome-Garcia, Jessica;
- Cheng, Wan Sze;
- Nudelman, German;
- Beaumont, Kristin G.;
- Ghatan, Saadi;
- Panov, Fedor;
- Caballero, Elodia;
- Sarpong, Kwadwo;
- Marcuse, Lara;
- Yoo, Jiyeoun;
- Jiang, Yan;
- Schaefer, Anne;
- Akbarian, Schahram;
- Sebra, Robert;
- Pinto, Dalila;
- Zaslavsky, Elena;
- Tsankova, Nadejda M.
Publication type:
Article
Association Analysis of BRD2 (RING3) and Epilepsy in a Dutch Population.
Published in:
2007
By:
- de Kovel, Carolien G. F.;
- Pinto, Dalila;
- de Haan, Gerrit J.;
- Trenité, Dorothée G. Kasteleijn-Nolst;
- Lindhout, Dick;
- Koeleman, Bobby P. C.
Publication type:
Letter
Heterogeneity at the JME 6p11–12 Locus: Absence of Mutations in the EFHC1 Gene in Linked Dutch Families.
Published in:
Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1743, doi. 10.1111/j.1528-1167.2006.00676.x
By:
- Pinto, Dalila;
- Louwaars, Sandrien;
- Westland, Birgit;
- Volkers, Linda;
- de Haan, Gerrit-Jan;
- Trenité, Dorothée G.A. Kasteleijn-Nolst;
- Lindhout, Dick;
- Koeleman, Bobby P. C.
Publication type:
Article
A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years.
Published in:
Epilepsia (Series 4), 2006, v. 47, n. 5, p. 851, doi. 10.1111/j.1528-1167.2006.00552.x
By:
- de Haan, Gerrit-Jan;
- Pinto, Dalila;
- Carton, Dietbrandt;
- Bader, Adri;
- Witte, Jorien;
- Peters, Edith;
- van Erp, Gerard;
- Vandereyken, Willem;
- Boezeman, Eduard;
- Wapenaar, Martin C.;
- Boon, Paul;
- Halley, Dicky;
- Koeleman, Bobby P. C.;
- Lindhout, Dick
Publication type:
Article
Evidence for Linkage between Juvenile Myoclonic Epilepsy–Related Idiopathic Generalized Epilepsy and 6p11-12 in Dutch Families.
Published in:
Epilepsia (Series 4), 2004, v. 45, n. 3, p. 211, doi. 10.1111/j.0013-9580.2004.36003.x
By:
- Pinto, Dalila;
- de Haan, Gerrit-Jan;
- Janssen, Guus A.M.A.J.;
- Boezeman, Eduard H.;
- van Erp, M. Gerard;
- Westland, Birgit;
- Witte, Jorine;
- Badder, Adri;
- Halley, Dicky J.J.;
- Trenite, Dorothee G.A. Kasteleijn-Nolst;
- Lindhout, Dick;
- Koeleman, Bobby P.C.
Publication type:
Article
Genetics of Photosensitivity (Photoparoxysmal Response): A Review.
Published in:
Epilepsia (Series 4), 2004, v. 45, p. 19, doi. 10.1111/j.0013-9580.2004.451008.x
By:
- Stephani, Ulrich;
- Tauer, Ulrike;
- Koeleman, Bobby;
- Pinto, Dalila;
- Neubauer, Bernd A.;
- Lindhout, Dick
Publication type:
Article
De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.
Published in:
American Journal of Medical Genetics. Part A, 2017, v. 173, n. 6, p. 1656, doi. 10.1002/ajmg.a.38171
By:
- Sagar, Angela;
- Pinto, Dalila;
- Najjar, Fedra;
- Guter, Stephen J.;
- Macmillan, Carol;
- Cook, Edwin H.
Publication type:
Article
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.
Published in:
Nature Biotechnology, 2011, v. 29, n. 6, p. 512, doi. 10.1038/nbt.1852
By:
- Pinto, Dalila;
- Darvishi, Katayoon;
- Xinghua Shi;
- Rajan, Diana;
- Rigler, Diane;
- Fitzgerald, Tom;
- Lionel, Anath C.;
- Thiruvahindrapuram, Bhooma;
- MacDonald, Jeffrey R.;
- Mills, Ryan;
- Prasad, Aparna;
- Noonan, Kristin;
- Gribble, Susan;
- Prigmore, Elena;
- Donahoe, Patricia K.;
- Smith, Richard S.;
- Ji Hyeon Park;
- Hurles, Matthew E.;
- Carter, Nigel P.;
- Lee, Charles
Publication type:
Article
Identification of novel genetic causes of Rett syndrome-like phenotypes by whole exome sequencing.
Published in:
International Journal of Developmental Neuroscience, 2015, v. 47, p. 99, doi. 10.1016/j.ijdevneu.2015.04.269
By:
- Lopes, Fátima;
- Barbosa, Mafalda;
- Temudo, Teresa;
- de Sá, Joaquim;
- Dias, Ana Isabel;
- Oliveira, Guiomar;
- Cabral, Pedro;
- Calado, Eulália;
- Cruz, Isabel Fineza;
- Soares, Gabriela;
- Vieira, José Pedro;
- Venâncio, Maria Margarida;
- Oliveira, Renata;
- Jonasson, Inger;
- Ameur, Adam;
- Pinto, Dalila;
- Ulf Gyllensten, null;
- Maciel, Patrícia
Publication type:
Article
Parallel changes in serum proteins and diffusion tensor imaging in methamphetamine-associated psychosis.
Published in:
Scientific Reports, 2017, p. 43777, doi. 10.1038/srep43777
By:
- Breen, Michael S.;
- Uhlmann, Anne;
- Ozcan, Sureyya;
- Chan, Man;
- Pinto, Dalila;
- Bahn, Sabine;
- Stein, Dan J.
Publication type:
Article

Found: 42