日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Overexpression of SOX3 due to an X chromosome inversion leading to ovotesticular difference in sex development

由于X染色体倒位导致SOX3过度表达,进而引起性发育中的卵睾差异

Nascimento-Vidoti, Carolina Gama; Fabbri-Scallet, Helena; Guaragna, Mara Sanches; de Wallau, Melissa Bittencourt; de Souza, Vanessa Sodré; da Costa, Silvia Souza; Krepischi, Ana Cristina Victorino; Mazzeu, Juliana Forte; Carvalho, Claudia M B; Maciel-Guerra, Andréa Trevas; Guerra-Júnior, Gil; Vieira, Társis Paiva

Clinical, in vitro, and in vivo evidence of WAPL as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder

临床、体外和体内证据表明,WAPL 是一种新的黏连蛋白病基因,也是 10q22.3q23.2 基因组疾病的表型驱动因素。

Boone, Philip M; Erdin, Serkan; Mohamed, Abucar; Haghshenas, Sadegheh; Faour, Kamli N W; Kao, Emeline; Fu, Jack; Auwerx, Chiara; Harripaul, Ricardo; Jana, Bimal; Springer, Danielle; Hallstrom, Grey; de Esch, Celine E F; Denhoff, Erica; Holmes, Lauren; Mohajeri, Kiana; Lemanski, John; Kerkhof, Jennifer; McConkey, Haley; Rzasa, Jessica; McCune, Madison J; Levy, Michael A; Grafstein, Julia; Larson, Matthew; Wright, Zsabre; Beauchamp, Roberta L; Lucente, Diane; Jamra, Rami Abou; Agrawal, Neena; Agrawal, Pankaj; Andersen, Erica F; Argilli, Emanuela; Araiza, Renee; Ballal, Sonia; Baxter, Megan F; Bergant, Gaber; Bertsche, Astrid; Bhavsar, Riya; Bortola, Debora R; Bothe, Viktoria; Brasch-Andersen, Charlotte; Braun, Dominique; Bruel, Ange-Line; Buchanan, Catherine; Burt, Nicholas D; Carvalho, Laura M L; Chiriatti, Luigi; Cogne, Benjamin; Collins, Ryan; Crunk, Amy; Currall, Benjamin; Delahaye-Duriez, Andree; Delanne, Julian; Denommé-Pichon, Anne-Sophie; Devriendt, Koenraad; Domingo, Aloysius; Duncan, Laura; Faivre, Laurence; Famularo, Laura; Fulton, Anne; Genetti, Casie; Harel, Tamar; Havlovicova, Marketa; Higgs, Jenny; Houlier, Marine; Iascone, Maria; Immken, LaDonna; Isidor, Bertrand; Kaiser, Frank J; Karbone, Kaycee; Kenna, Margaret; Khan, Amjad; Kimmig, Lara Kristina; Kleefstra, Tjitske; Kraus, Eva-Maria; Krepischi, Ana C V; Krey, Ilona; Ladda, Roger; Lanoue, Louise; Le Caignec, Cedric; Lewis, Zoe K; Lima, Gloria; Lynch, Sally Ann; Macek, Milan Jr; Maier, Olivier; Maitz, Silvia; Male, Alison; Malikova, Marcela; McKay, Victoria; Moldovan, Oana; Monteil, Danielle; Oliveira, Mariana Moysés; Munasinghe, Jeeva; Nakamori, Sachiko; Neuser, Sonja; Nizon, Mathilde; Nuttle, Xander; O'Keefe, Kathryn; Orec, Laura; Parenti, Ilaria; Peterlin, Borut; Pfundt, Rolph; Pouncey, Jill; Radio, Francesca Clementina; Robert, Leema; Rodan, Lance; Rosenberg-Fogler, Hallel; Rosenfeld, Jill A; Safraou, Hana; Salani, Monica; Schliesske, Sophia; Seaby, Eleanor G; Sell, Susan; Eliot Shearer, A; Sherr, Elliott; Shillington, Amelle; Siebold, Dorothea; Sinnema, Margje; Smith, Laura; Stegmann, Alexander P A; Stevens, Cathy; Stevens, Servi; Surette, Eric; Tartaglia, Marco; Taylor, Jenny C; Thompson, Michelle L; Tørring, Pernille M; Mau Them, Frederic Tran; Tsoulaki, Olga; Umair, Muhammad; Vanhoutte, Els; Vincent, Marie; Vitobello, Antonio; von Wintzingerode, Lydia; Watt, Amy; Wayhelova, Marketa; Wentzensen, Ingrid M; Wilson, William; Wojcik, Monica H; Yuan, Bo; Zampino, Giuseppe; Srivastava, Siddharth; Westphal, Dominik S; Riedhammer, Korbinian M; Joyce, Eric; Yadav, Rachita; Gusella, James; Tai, Derek J C; Sadikovic, Bekim; Pfeifer, Karl E; Talkowski, Michael E

Understanding rare variant contributions to autism: lessons from dystrophin-deficient model

了解罕见变异对自闭症的影响:来自肌营养不良蛋白缺陷模型的启示

Costa, Claudia Ismania Samogy; Madanelo, Luciana; Wang, Jaqueline Yu Ting; da Silva Campos, Gabriele; De Sanctis Girardi, Ana Cristina; Scliar, Marília; Monfardini, Frederico; de Cássia Mingroni Pavanello, Rita; Cória, Vivian Romanholi; Vibranovski, Maria Dulcetti; Krepischi, Ana Cristina; Lourenço, Naila Cristina Vilaça; Zatz, Mayana; Yamamoto, Guilherme Lopes; Zachi, Elaine Cristina; Passos-Bueno, Maria Rita

Differential methylation in blood pressure control genes is associated to essential hypertension in African Brazilian populations

非洲裔巴西人群中血压控制基因的差异甲基化与原发性高血压相关

Avila Martins, Camila Cristina; Maschietto, Mariana; Kimura, Lilian; Alvizi, Lucas; Nunes, Kelly; Magalhães Borges, Vinícius; Victorino Krepischi, Ana Cristina; Mingroni-Netto, Regina Célia

Exome sequencing of patients with syndromic tall stature reveals four novel candidate genes

对患有综合征性高大症的患者进行外显子组测序,发现了四个新的候选基因。

Kim, Gabriela Jeesoo; Vasco de Albuquerque Albuquerque, Edoarda; Rezende, Raissa C; De Polli Cellin, Laurana; Santillan Vasconez, Ana Maria; Krepischi, Ana C V; Santana, Lucas; Lerario, Antônio Marcondes; de Souza, Vinicius; Scalco, Renata; Jorge, Alexander A L

SMC6 expression & outcome of breast cancer

SMC6表达与乳腺癌预后

Mangone, Flavia Regina Rotea; Krepischi, Ana Cristina Victorino; Pavanelli, Ana Carolina; Gatti, Pedro Henrique Fernandes; Carraro, Dirce Maria; Nagai, Maria A

Clinical and Molecular Characterization of Xia-Gibbs Syndrome: Expanding the Phenotypic Spectrum in a Brazilian Cohort

Xia-Gibbs综合征的临床和分子特征:扩展巴西人群的表型谱

Sennes, Maísa Ganz Sanchez; Carvalho, Laura Machado Lara; Castro, Matheus Augusto Araújo; Toccoli, Giovana Manilli; Farias, Sofia de Oliveira; Fialho, Davi Mendes Campo; Bertollo, Eny Maria Goloni; Pavarino, Erika Cristina; de Athayde, Larissa Sampaio; Buck, Cecilia Barbosa; Toralles, Maria Betânia Pereira; Melaragno, Maria Isabel; Riegel-Giugliani, Mariluce; Spolador, Gustavo Marquezani; Otto, Paulo Alberto; Piai, Caroline Brandão; Kok, Fernando; Cechella, Ceres Schmitz; Rosenberg, Carla; Llerena, Juan Clinton; Bertola, Débora Romeo; Raskin, Salmo; Kim, Chong Ae; Krepischi, Ana Cristina Victorino

AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions

AP2M1是3q27.1缺失导致小头畸形和智力障碍的候选基因

Gear, Russell; Kalitsis, Paul; Glass, Melissa; Isidor, Bertrand; Vincent-Delorme, Catherine; Petit, Florence; Verhagen, Judith M A; Jorge, Alexander; Krepischi, Ana Cristina Victorino; Osei-Owusu, Ikeoluwa; Martinez, Eva; O'Donnell-Luria, Anne; de Leeuw, Nicole; Ruggiero, Sarah; Helbig, Ingo; David, Francis 1st; Brown, Natasha J

A Complex Chromosome Rearrangement Disrupting SYT1 Supports Haploinsufficiency as a Cause of Baker-Gordon Syndrome

复杂的染色体重排破坏了SYT1基因,这支持了单倍体不足是贝克-戈登综合征病因的观点。

Bertola, Débora Romeo; Farias, Sofia de Oliveira; da Costa, Silvia Souza; Pinheiro, Mara Maria Lisboa Santana; Passos-Bueno, Maria Rita Dos Santos; Rosenberg, Carla; Krepischi, Ana Cristina Victorino

Distinct copy number signatures between residual benign and transformed areas of carcinoma ex pleomorphic adenoma

多形性腺瘤癌变后残留良性区域和转化区域之间存在不同的拷贝数特征。

Scarini, João Figueira; Sabino, Wellington Lima; de Lima-Souza, Reydson Alcides; Egal, Erika Said Abu; Tincani, Alfio José; Gondak, Rogério; Kowalski, Luiz Paulo; Krepischi, Ana Cristina Victorino; Altemani, Albina; Mariano, Fernanda Viviane