Pesquisa | BVS IEC

1.

Infant microbes and metabolites point to childhood neurodevelopmental disorders.

Ahrens, Angelica P; Hyötyläinen, Tuulia; Petrone, Joseph R; Igelström, Kajsa; George, Christian D; Garrett, Timothy J; Oresic, Matej; Triplett, Eric W; Ludvigsson, Johnny.

Cell ; 187(8): 1853-1873.e15, 2024 Apr 11.

Artigo em Inglês | MEDLINE | ID: mdl-38574728

2.

Prenatal and postnatal neuroimmune interactions in neurodevelopmental disorders.

Kim, Eunha; Huh, Jun R; Choi, Gloria B.

Nat Immunol ; 25(4): 598-606, 2024 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-38565970

3.

SnapShot: The microbiota-gut-brain axis.

Agirman, Gulistan; Hsiao, Elaine Y.

Cell ; 184(9): 2524-2524.e1, 2021 04 29.

Artigo em Inglês | MEDLINE | ID: mdl-33930299

4.

Dissecting the contribution of host genetics and the microbiome in complex behaviors.

Buffington, Shelly A; Dooling, Sean W; Sgritta, Martina; Noecker, Cecilia; Murillo, Oscar D; Felice, Daniela F; Turnbaugh, Peter J; Costa-Mattioli, Mauro.

Cell ; 184(7): 1740-1756.e16, 2021 04 01.

Artigo em Inglês | MEDLINE | ID: mdl-33705688

5.

Interleukin-17: A Social Cytokine.

Hoogenraad, Casper C; Riol-Blanco, Lorena.

Cell ; 181(3): 517-519, 2020 04 30.

Artigo em Inglês | MEDLINE | ID: mdl-32359435

6.

Gene regulation by long non-coding RNAs and its biological functions.

Statello, Luisa; Guo, Chun-Jie; Chen, Ling-Ling; Huarte, Maite.

Nat Rev Mol Cell Biol ; 22(2): 96-118, 2021 02.

Artigo em Inglês | MEDLINE | ID: mdl-33353982

7.

The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.

Willsey, A Jeremy; Morris, Montana T; Wang, Sheng; Willsey, Helen R; Sun, Nawei; Teerikorpi, Nia; Baum, Tierney B; Cagney, Gerard; Bender, Kevin J; Desai, Tejal A; Srivastava, Deepak; Davis, Graeme W; Doudna, Jennifer; Chang, Edward; Sohal, Vikaas; Lowenstein, Daniel H; Li, Hao; Agard, David; Keiser, Michael J; Shoichet, Brian; von Zastrow, Mark; Mucke, Lennart; Finkbeiner, Steven; Gan, Li; Sestan, Nenad; Ward, Michael E; Huttenhain, Ruth; Nowakowski, Tomasz J; Bellen, Hugo J; Frank, Loren M; Khokha, Mustafa K; Lifton, Richard P; Kampmann, Martin; Ideker, Trey; State, Matthew W; Krogan, Nevan J.

Cell ; 174(3): 505-520, 2018 07 26.

Artigo em Inglês | MEDLINE | ID: mdl-30053424

8.

Maternal gut bacteria drive intestinal inflammation in offspring with neurodevelopmental disorders by altering the chromatin landscape of CD4⁺ T cells.

Kim, Eunha; Paik, Donggi; Ramirez, Ricardo N; Biggs, Delaney G; Park, Youngjun; Kwon, Ho-Keun; Choi, Gloria B; Huh, Jun R.

Immunity ; 55(1): 145-158.e7, 2022 01 11.

Artigo em Inglês | MEDLINE | ID: mdl-34879222

9.

The Central Nervous System and the Gut Microbiome.

Sharon, Gil; Sampson, Timothy R; Geschwind, Daniel H; Mazmanian, Sarkis K.

Cell ; 167(4): 915-932, 2016 11 03.

Artigo em Inglês | MEDLINE | ID: mdl-27814521

10.

Human Cerebellar Development and Transcriptomics: Implications for Neurodevelopmental Disorders.

Haldipur, Parthiv; Millen, Kathleen J; Aldinger, Kimberly A.

Annu Rev Neurosci ; 45: 515-531, 2022 07 08.

Artigo em Inglês | MEDLINE | ID: mdl-35440142

11.

Microglia and Neurodevelopmental Disorders.

Lukens, John R; Eyo, Ukpong B.

Annu Rev Neurosci ; 45: 425-445, 2022 07 08.

Artigo em Inglês | MEDLINE | ID: mdl-35436413

12.

Mechanisms Underlying Circuit Dysfunction in Neurodevelopmental Disorders.

Exposito-Alonso, David; Rico, Beatriz.

Annu Rev Genet ; 56: 391-422, 2022 11 30.

Artigo em Inglês | MEDLINE | ID: mdl-36055969

13.

Assembloid CRISPR screens reveal impact of disease genes in human neurodevelopment.

Meng, Xiangling; Yao, David; Imaizumi, Kent; Chen, Xiaoyu; Kelley, Kevin W; Reis, Noah; Thete, Mayuri Vijay; Arjun McKinney, Arpana; Kulkarni, Shravanti; Panagiotakos, Georgia; Bassik, Michael C; PaÈca, Sergiu P.

Nature ; 622(7982): 359-366, 2023 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-37758944

14.

A trivalent nucleosome interaction by PHIP/BRWD2 is disrupted in neurodevelopmental disorders and cancer.

Morgan, Marc A J; Popova, Irina K; Vaidya, Anup; Burg, Jonathan M; Marunde, Matthew R; Rendleman, Emily J; Dumar, Zachary J; Watson, Rachel; Meiners, Matthew J; Howard, Sarah A; Khalatyan, Natalia; Vaughan, Robert M; Rothbart, Scott B; Keogh, Michael-C; Shilatifard, Ali.

Genes Dev ; 35(23-24): 1642-1656, 2021 12 01.

Artigo em Inglês | MEDLINE | ID: mdl-34819353

15.

Rare coding variants in ten genes confer substantial risk for schizophrenia.

Singh, Tarjinder; Poterba, Timothy; Curtis, David; Akil, Huda; Al Eissa, Mariam; Barchas, Jack D; Bass, Nicholas; Bigdeli, Tim B; Breen, Gerome; Bromet, Evelyn J; Buckley, Peter F; Bunney, William E; Bybjerg-Grauholm, Jonas; Byerley, William F; Chapman, Sinéad B; Chen, Wei J; Churchhouse, Claire; Craddock, Nicholas; Cusick, Caroline M; DeLisi, Lynn; Dodge, Sheila; Escamilla, Michael A; Eskelinen, Saana; Fanous, Ayman H; Faraone, Stephen V; Fiorentino, Alessia; Francioli, Laurent; Gabriel, Stacey B; Gage, Diane; Gagliano Taliun, Sarah A; Ganna, Andrea; Genovese, Giulio; Glahn, David C; Grove, Jakob; Hall, Mei-Hua; Hämäläinen, Eija; Heyne, Henrike O; Holi, Matti; Hougaard, David M; Howrigan, Daniel P; Huang, Hailiang; Hwu, Hai-Gwo; Kahn, René S; Kang, Hyun Min; Karczewski, Konrad J; Kirov, George; Knowles, James A; Lee, Francis S; Lehrer, Douglas S; Lescai, Francesco.

Nature ; 604(7906): 509-516, 2022 04.

Artigo em Inglês | MEDLINE | ID: mdl-35396579

16.

Strategies for dissecting the complexity of neurodevelopmental disorders.

Sun, Jiawan; Noss, Serena; Banerjee, Deepro; Das, Maitreya; Girirajan, Santhosh.

Trends Genet ; 40(2): 187-202, 2024 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-37949722

17.

Immune synaptopathies: how maternal immune activation impacts synaptic function during development.

Matteoli, Michela; Pozzi, Davide; Fossati, Matteo; Menna, Elisabetta.

EMBO J ; 42(13): e113796, 2023 07 03.

Artigo em Inglês | MEDLINE | ID: mdl-37161785

18.

Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases.

Torene, Rebecca I; Guillen Sacoto, Maria J; Millan, Francisca; Zhang, Zhancheng; McGee, Stephen; Oetjens, Matthew; Heise, Elizabeth; Chong, Karen; Sidlow, Richard; O'Grady, Lauren; Sahai, Inderneel; Martin, Christa L; Ledbetter, David H; Myers, Scott M; Mitchell, Kevin J; Retterer, Kyle.

Am J Hum Genet ; 111(1): 70-81, 2024 Jan 04.

Artigo em Inglês | MEDLINE | ID: mdl-38091987

19.

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.

Salpietro, Vincenzo; Maroofian, Reza; Zaki, Maha S; Wangen, Jamie; Ciolfi, Andrea; Barresi, Sabina; Efthymiou, Stephanie; Lamaze, Angelique; Aughey, Gabriel N; Al Mutairi, Fuad; Rad, Aboulfazl; Rocca, Clarissa; Calì, Elisa; Accogli, Andrea; Zara, Federico; Striano, Pasquale; Mojarrad, Majid; Tariq, Huma; Giacopuzzi, Edoardo; Taylor, Jenny C; Oprea, Gabriela; Skrahina, Volha; Rehman, Khalil Ur; Abd Elmaksoud, Marwa; Bassiony, Mahmoud; El Said, Huda G; Abdel-Hamid, Mohamed S; Al Shalan, Maha; Seo, Gohun; Kim, Sohyun; Lee, Hane; Khang, Rin; Issa, Mahmoud Y; Elbendary, Hasnaa M; Rafat, Karima; Marinakis, Nikolaos M; Traeger-Synodinos, Joanne; Ververi, Athina; Sourmpi, Mara; Eslahi, Atieh; Khadivi Zand, Farhad; Beiraghi Toosi, Mehran; Babaei, Meisam; Jackson, Adam; Bertoli-Avella, Aida; Pagnamenta, Alistair T; Niceta, Marcello; Battini, Roberta; Corsello, Antonio; Leoni, Chiara.

Am J Hum Genet ; 111(1): 200-210, 2024 Jan 04.

Artigo em Inglês | MEDLINE | ID: mdl-38118446

20.

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.

Paul, Maimuna S; Michener, Sydney L; Pan, Hongling; Chan, Hiuling; Pfliger, Jessica M; Rosenfeld, Jill A; Lerma, Vanesa C; Tran, Alyssa; Longley, Megan A; Lewis, Richard A; Weisz-Hubshman, Monika; Bekheirnia, Mir Reza; Bekheirnia, Nasim; Massingham, Lauren; Zech, Michael; Wagner, Matias; Engels, Hartmut; Cremer, Kirsten; Mangold, Elisabeth; Peters, Sophia; Trautmann, Jessica; Mester, Jessica L; Guillen Sacoto, Maria J; Person, Richard; McDonnell, Pamela P; Cohen, Stacey R; Lusk, Laina; Cohen, Ana S A; Le Pichon, Jean-Baptiste; Pastinen, Tomi; Zhou, Dihong; Engleman, Kendra; Racine, Caroline; Faivre, Laurence; Moutton, Sébastien; Denommé-Pichon, Anne-Sophie; Koh, Hyun Yong; Poduri, Annapurna; Bolton, Jeffrey; Knopp, Cordula; Julia Suh, Dong Sun; Maier, Andrea; Toosi, Mehran Beiraghi; Karimiani, Ehsan Ghayoor; Maroofian, Reza; Schaefer, Gerald Bradley; Ramakumaran, Vijayalakshmi; Vasudevan, Pradeep; Prasad, Chitra; Osmond, Matthew.

Am J Hum Genet ; 111(1): 96-118, 2024 Jan 04.

Artigo em Inglês | MEDLINE | ID: mdl-38181735

BVS IEC

Instituto Evandro Chagas

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