المؤلفون: Griesi-Oliveira, Karina, Sertié, Andréa Laurato

المصدر: einstein (São Paulo). June 2017 15(2)

مصطلحات موضوعية: Autistic disorder, Genetic counseling, Microarray analysis, Genetic testing, Pathology, molecular

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082017000200233

المؤلفون: Teles e Silva, André Luíz, Glaser, Talita, Griesi-Oliveira, Karina, Corrêa-Velloso, Juliana, Wang, Jaqueline Yu Ting, da Silva Campos, Gabriele, Ulrich, Henning, Balan, Andrea, Zarrei, Mehdi, Higginbotham, Edward J., Scherer, Stephen W., Passos-Bueno, Maria Rita, Sertié, Andrea Laurato

المصدر: Translational Psychiatry ; volume 12, issue 1 ; ISSN 2158-3188

الاتاحة: http://dx.doi.org/10.1038/s41398-022-01997-9
https://www.nature.com/articles/s41398-022-01997-9.pdf
https://www.nature.com/articles/s41398-022-01997-9

المؤلفون: Moreira, Danielle de Paula, Suzuki, Angela May, Silva, André Luiz Teles e, Varella-Branco, Elisa, Meneghetti, Maria Cecília Zorél, Kobayashi, Gerson Shigeru, Fogo, Mariana, Ferrari, Merari de Fátima Ramires, Cardoso, Rafaela Regina, Lourenço, Naila Cristina Vilaça, Griesi-Oliveira, Karina, Zachi, Elaine Cristina, Bertola, Débora Romeo, Weinmann, Karina de Souza, Lima, Marcelo Andrade de, Nader, Helena Bonciani, Sertié, Andrea Laurato, Passos-Bueno, Maria Rita

المساهمون: Fundação de Amparo à Pesquisa do Estado de São Paulo, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

المصدر: Frontiers in Cellular Neuroscience ; volume 15 ; ISSN 1662-5102

الاتاحة: http://dx.doi.org/10.3389/fncel.2021.803302
https://www.frontiersin.org/articles/10.3389/fncel.2021.803302/full

المؤلفون: Tomaz, Victória, Griesi-Oliveira, Karina, Puga, Renato D., Conti, Bruno J., Santos, Fabio P. S., Hamerschlak, Nelson, Campregher, Paulo V.

المصدر: Frontiers in Oncology ; volume 12 ; ISSN 2234-943X

الاتاحة: http://dx.doi.org/10.3389/fonc.2022.874168
https://www.frontiersin.org/articles/10.3389/fonc.2022.874168/full

المؤلفون: Gomes, Ana Karolyne Santos, Dantas, Rafaelly Mayara, Yokota, Bruno Yukio, Silva, André Luiz Teles e, Griesi-Oliveira, Karina, Passos-Bueno, Maria Rita, Sertié, Andréa Laurato

المساهمون: Fundação de Amparo à Pesquisa do Estado de São Paulo, Conselho Nacional de Desenvolvimento Científico e Tecnológico

المصدر: Frontiers in Neuroscience ; volume 16 ; ISSN 1662-453X

الاتاحة: http://dx.doi.org/10.3389/fnins.2022.828646
https://www.frontiersin.org/articles/10.3389/fnins.2022.828646/full

المؤلفون: Melo, Uirá S, Macedo-Souza, Lucia I, Figueiredo, Thalita, Muotri, Alysson R, Gleeson, Joseph G, Coux, Gabriela, Armas, Pablo, Calcaterra, Nora B, Kitajima, João P, Amorim, Simone, Olávio, Thiago R, Griesi-Oliveira, Karina, Coatti, Giuliana C, Rocha, Clarissa RR, Martins-Pinheiro, Marinalva, Menck, Carlos FM, Zaki, Maha S, Kok, Fernando, Zatz, Mayana, Santos, Silvana

المصدر: Human Molecular Genetics. 24(24)

مصطلحات موضوعية: Biological Sciences, Genetics, Clinical Research, Biotechnology, Human Genome, Brain Disorders, Neurosciences, Pediatric, Rare Diseases, Neurodegenerative, Aetiology, 2.1 Biological and endogenous factors, Neurological, Animals, Chromosomes, Human, Pair 11, DNA Mutational Analysis, Gene Expression, Hereditary Sensory and Motor Neuropathy, Humans, Kinesins, Microtubule-Associated Proteins, Optic Atrophies, Hereditary, Sequence Deletion, Spastic Paraplegia, Hereditary, Syndrome, Zebrafish, Zebrafish Proteins, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/5hb0q03q

المؤلفون: Ravagnani, Felipe G., Valerio, Hellen P., Maués, Jersey H.S., de Oliveira, Arthur N., Puga, Renato D., Griesi-Oliveira, Karina, Picosse, Fabíola R., Ferraz, Henrique B., Catharino, Rodrigo R., Ronsein, Graziella E., de Carvalho Aguiar, Patrícia

المصدر: Parkinsonism & Related Disorders ; volume 116, page 105847 ; ISSN 1353-8020

الاتاحة: http://dx.doi.org/10.1016/j.parkreldis.2023.105847
https://api.elsevier.com/content/article/PII:S1353802023009264?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1353802023009264?httpAccept=text/plain

المؤلفون: de Carvalho Aguiar, Patricia, Ravagnani, Felipe, Maues, Jersey Heitor, Puga, Renato David, Griesi-Oliveira, Karina

مصطلحات موضوعية: Neurodegenerative Disorder, RNA, Induced Pluripotent Stem Cell, Astrocyte, Progressive Supranuclear Palsy, Transcriptomics

Relation: https://dx.doi.org/10.17632/wwwrzhbz59

الاتاحة: https://dx.doi.org/10.17632/wwwrzhbz59.1
https://data.mendeley.com/datasets/wwwrzhbz59/1

المؤلفون: Caires-Júnior, Luiz Carlos, Goulart, Ernesto, Melo, Uirá Souto, Araujo, Bruno Henrique Silva, Alvizi, Lucas, Soares-Schanoski, Alessandra, de Oliveira, Danyllo Felipe, Kobayashi, Gerson Shigeru, Griesi-Oliveira, Karina, Musso, Camila Manso, Amaral, Murilo Sena, daSilva, Lucas Ferreira, Astray, Renato Mancini, Suárez-Patiño, Sandra Fernanda, Ventini, Daniella Cristina, Gomes da Silva, Sérgio, Yamamoto, Guilherme Lopes, Ezquina, Suzana, Naslavsky, Michel Satya, Telles-Silva, Kayque Alves, Weinmann, Karina, van der Linden, Vanessa, van der Linden, Helio, de Oliveira, João Ricardo Mendes, Arrais, Nivia Maria Rodrigues, Melo, Adriana, Figueiredo, Thalita, Santos, Silvana, Meira, Joanna Goes Castro, Passos, Saulo Duarte, de Almeida, Roque Pacheco, Bispo, Ana Jovina Barreto, Cavalheiro, Esper Abrão, Kalil, Jorge, Cunha-Neto, Edécio, Nakaya, Helder, Andreata-Santos, Robert, de Souza Ferreira, Luis Carlos, Verjovski-Almeida, Sergio, Ho, Paulo Lee, Passos-Bueno, Maria Rita, Zatz, Mayana

المصدر: Nature Communications ; volume 9, issue 1 ; ISSN 2041-1723

الاتاحة: http://dx.doi.org/10.1038/s41467-017-02790-9
https://www.nature.com/articles/s41467-017-02790-9
https://www.nature.com/articles/s41467-017-02790-9.pdf

المؤلفون: Griesi-Oliveira, Karina, Suzuki, Angela May, Alves, Aline Yasuda, Mafra, Ana Carolina Cintra Nunes, Yamamoto, Guilherme Lopes, Ezquina, Suzana, Magalhães, Yuli Thamires, Forti, Fabio Luis, Sertie, Andrea Laurato, Zachi, Elaine Cristina, Vadasz, Estevão, Passos-Bueno, Maria Rita

المصدر: Scientific Reports ; volume 8, issue 1 ; ISSN 2045-2322

الاتاحة: http://dx.doi.org/10.1038/s41598-018-29309-6
https://www.nature.com/articles/s41598-018-29309-6.pdf
https://www.nature.com/articles/s41598-018-29309-6

المؤلفون: Caires-Júnior, Luiz Carlos, Goulart, Ernesto, Melo, Uirá Souto, Araujo, Bruno Henrique Silva, Alvizi, Lucas, Soares-Schanoski, Alessandra, de Oliveira, Danyllo Felipe, Kobayashi, Gerson Shigeru, Griesi-Oliveira, Karina, Musso, Camila Manso, Amaral, Murilo Sena, daSilva, Lucas Ferreira, Astray, Renato Mancini, Suárez-Patiño, Sandra Fernanda, Ventini, Daniella Cristina, da Silva, Sérgio Gomes, Yamamoto, Guilherme Lopes, Ezquina, Suzana, Naslavsky, Michel Satya, Telles-Silva, Kayque Alves, Weinmann, Karina, van der Linden, Vanessa, van der Linden, Helio, de Oliveira, João Ricardo Mendes, Arrais, Nivia Maria Rodrigues, Melo, Adriana, Figueiredo, Thalita, Santos, Silvana, Meira, Joanna Goes Castro, Passos, Saulo Duarte, de Almeida, Roque Pacheco, Bispo, Ana Jovina Barreto, Cavalheiro, Esper Abrão, Kalil, Jorge, Cunha-Neto, Edécio, Nakaya, Helder, Andreata-Santos, Robert, de Souza Ferreira, Luis Carlos, Verjovski-Almeida, Sergio, Ho, Paulo Lee, Passos-Bueno, Maria Rita, Zatz, Mayana

المصدر: Nature Communications ; volume 9, issue 1 ; ISSN 2041-1723

الاتاحة: https://doi.org/10.1038/s41467-018-03497-1
https://www.nature.com/articles/s41467-018-03497-1.pdf
https://www.nature.com/articles/s41467-018-03497-1

المؤلفون: Moreira, Eloisa S., Silva, Isabela M. W., Lourenco, Naila, Moreira, Danielle P., Ribeiro, Cintia M., Martins, Ana Luiza B., Griesi-Oliveira, Karina, Lazar, Monize, Costa, Silvia S., Naslavsky, Michel S., Rocha, Katia M., Aguena, Meire, Fett-Conte, Agnes C., Zatz, Mayana, Rosenberg, Carla, Zachi, Elaine C., Bertola, Debora R., Vadasz, Estevao, Passos-Bueno, Maria Rita

المساهمون: Universidade Estadual Paulista (UNESP)

مصطلحات موضوعية: Autism, Copy number variation, Comparative genomic hybridization, Neurodevelopmental disorder, MBD2, SLC17A6

وصف الملف: 145-151

Relation: Research In Autism Spectrum Disorders; 0,844; http://dx.doi.org/10.1016/j.rasd.2015.12.012; Research In Autism Spectrum Disorders. Oxford: Elsevier Sci Ltd, v. 23, p. 145-151, 2016.; http://hdl.handle.net/11449/164712; WOS:000370303400013; WOS000370303400013.pdf

الاتاحة: http://hdl.handle.net/11449/164712
https://doi.org/10.1016/j.rasd.2015.12.012

المؤلفون: Machado, Camila Oliveira Freitas, Griesi-Oliveira, Karina, Rosenberg, Carla, Kok, Fernando, Martins, Stephanie, Rita Passos-Bueno, Maria, Sertie, Andrea Laurato

المصدر: European Journal of Human Genetics ; volume 24, issue 1, page 59-65 ; ISSN 1018-4813 1476-5438

الاتاحة: http://dx.doi.org/10.1038/ejhg.2015.69
http://www.nature.com/articles/ejhg201569.pdf
http://www.nature.com/articles/ejhg201569

المؤلفون: Melo, Uirá S., Macedo-Souza, Lucia I., Figueiredo, Thalita, Muotri, Alysson R., Gleeson, Joseph G., Coux, Gabriela, Armas, Pablo, Calcaterra, Nora B., Kitajima, João P., Amorim, Simone, Olávio, Thiago R., Griesi-Oliveira, Karina, Coatti, Giuliana C., Rocha, Clarissa R.R., Martins-Pinheiro, Marinalva, Menck, Carlos F.M., Zaki, Maha S., Kok, Fernando, Zatz, Mayana, Santos, Silvana

المساهمون: Propesq/UEPB, PPSUS/FAPESQ/PB, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Instituto Nacional de Ciência e Tecnologia (INCT), Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), Centro de Pesquisa, Inovação e Difusão (CEPID)

المصدر: Human Molecular Genetics ; page ddv388 ; ISSN 0964-6906 1460-2083

الاتاحة: http://dx.doi.org/10.1093/hmg/ddv388
http://academic.oup.com/hmg/article-pdf/24/24/6877/17262298/ddv388.pdf

المؤلفون: Griesi‐Oliveira, Karina, Sunaga, Daniele Yumi, Cruz, Lucas Alvizi, Vadasz, Estevão, Passos‐Bueno, Maria Rita

المصدر: Autism Research ; volume 8, issue 1, page 121-121 ; ISSN 1939-3792 1939-3806

الاتاحة: http://dx.doi.org/10.1002/aur.1330
http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Faur.1330
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Faur.1330
https://onlinelibrary.wiley.com/doi/pdf/10.1002/aur.1330

المؤلفون: Griesi-Oliveira, Karina, Suzuki, Angela May, Muotri, Alysson Renato

المصدر: Advances in Experimental Medicine and Biology ; Transient Receptor Potential Canonical Channels and Brain Diseases ; page 137-148 ; ISSN 0065-2598 2214-8019 ; ISBN 9789402410860 9789402410884

الاتاحة: http://dx.doi.org/10.1007/978-94-024-1088-4_12
http://link.springer.com/content/pdf/10.1007/978-94-024-1088-4_12

المؤلفون: Sánchez-Sánchez, Sandra M., Magdalon, Juliana, Griesi-Oliveira, Karina, Yamamoto, Guilherme L., Santacruz-Perez, Carolina, Fogo, Mariana, Passos-Bueno, Maria Rita, Sertié, Andrea L.

المساهمون: Sao Paulo Research Foundation (FAPESP)

المصدر: Human Mutation ; volume 39, issue 10, page 1372-1383 ; ISSN 1059-7794

الاتاحة: http://dx.doi.org/10.1002/humu.23584
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fhumu.23584
http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.23584/fullpdf

المؤلفون: Miller, Emily E., Kobayashi, Gerson S., Musso, Camila M., Allen, Miranda, Ishiy, Felipe A.A., de Caires, Luiz Carlos, Goulart, Ernesto, Griesi-Oliveira, Karina, Zechi-Ceide, Roseli M., Richieri-Costa, Antonio, Bertola, Debora R., Passos-Bueno, Maria Rita, Silver, Debra L.

المساهمون: NIH, NSF Graduate Research Fellowship, FAPESP/CEPID, CNPq

المصدر: Human Molecular Genetics ; volume 26, issue 12, page 2177-2191 ; ISSN 0964-6906 1460-2083

الاتاحة: http://dx.doi.org/10.1093/hmg/ddx078
http://academic.oup.com/hmg/article-pdf/26/12/2177/22772478/ddx078.pdf

المؤلفون: Griesi‐Oliveira, Karina, Sunaga, Daniele Yumi, Alvizi, Lucas, Vadasz, Estevão, Passos‐Bueno, Maria Rita

المصدر: Autism Research ; volume 6, issue 5, page 354-361 ; ISSN 1939-3792 1939-3806

الاتاحة: http://dx.doi.org/10.1002/aur.1296
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Faur.1296
https://onlinelibrary.wiley.com/doi/pdf/10.1002/aur.1296
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/aur.1296

المؤلفون: Griesi‐Oliveira, Karina, Moreira, Danielle de Paula, Davis‐Wright, Nicole, Sanders, Stephan, Mason, Christopher, Orabona, Guilherme Müller, Vadasz, Estevão, Bertola, Débora Romeo, State, Matthew W., Passos‐Bueno, Maria Rita

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ; volume 159B, issue 5, page 529-536 ; ISSN 1552-4841 1552-485X

الاتاحة: http://dx.doi.org/10.1002/ajmg.b.32059
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.b.32059
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.32059