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

Exome analysis links kidney malformations to developmental disorders and reveals causal genes

外显子组分析将肾脏畸形与发育障碍联系起来,并揭示了致病基因。

Milo Rasouly, Hila; Krishna Murthy, Sarath Babu; Vena, Natalie; Povysil, Gundula; Beenken, Andrew; Verbitsky, Miguel; Shril, Shirlee; Lekkerkerker, Iris; Yang, Sandy; Khan, Atlas; Fasel, David; Wongboonsin, Janewit; Martino, Jeremiah; Ke, Juntao; Elefant, Naama; Tomar, Nikita; Harnof, Ofek; Kisselev, Sergey; Bheda, Shiraz; Reytan-Miron, Sivan; Lim, Tze Y; Jamry-Dziurla, Anna; Lugani, Francesca; Zhang, Jun Y; Marasa, Maddalena; Kolupaeva, Victoria; Groopman, Emily E; Jin, Gina; Ghavami, Iman; Stevens, Kelsey O; Coughlin, Arielle C; Kil, Byum Hee; Chatterjee, Debanjana; Bradbury, Drew; Zheng, Jason; Mehl, Karla; Morban, Maria; Reingold, Rachel; Piva, Stacy; Mu, Xueru; Mitrotti, Adele; Szmigielska, Agnieszka; Gliwińska, Aleksandra; Ranghino, Andrea; Bomback, Andrew S; Badenski, Andrzej; Latos-Bielenska, Anna; Capone, Valentina; Materna-Kiryluk, Anna; Amoroso, Antonio; Izzi, Claudia; La Scola, Claudio; Cohen, David Jonathan; Santoro, Domenico; Drozdz, Dorota; Fiaccadori, Enrico; Lin, Fangming; Scolari, Francesco; Tondolo, Francesco; La Manna, Gaetano; Appel, Gerald B; Ghiggeri, Gian Marco; Zaza, Gianluigi; Montini, Giovanni; Masnata, Giuseppe; Krzemien, Grażyna; Pisani, Isabella; Radhakrishnan, Jai; Zachwieja, Katarzyna; Gesualdo, Loreto; Biancone, Luigi; Meneghesso, Davide; Mizerska-Wasiak, Malgorzata; Tkaczyk, Marcin; Zaniew, Marcin; Borszewska-Kornacka, Maria K; Szczepanska, Maria; Saraga, Marijan; Rao, Maya K; Bodria, Monica; Miklaszewska, Monika; Uy, Natalie S; Baraldi, Olga; Bjanid, Omar; Esposito, Pasquale; Zamboli, Pasquale; Marzuillo, Pierluigi; Canetta, Pietro A; Sikora, Przemyslaw; Westland, Rik; Crew, Russell J; Alam, Shumyle; Guarino, Stefano; Negrisolo, Susanna; Hays, Thomas; Mane, Shrikant; Grandinetti, Valeria; Tasic, Velibor; Lozanovski, Vladimir J; Caliskan, Yasar; Goldstein, David; Lifton, Richard P; Ionita-Laza, Iuliana; Kiryluk, Krzysztof; van Eerde, Albertien M; Hildebrandt, Friedhelm; Sanna-Cherchi, Simone; Gharavi, Ali G

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes

作者更正:外显子组分析将肾脏畸形与发育障碍联系起来,并揭示了致病基因

Milo Rasouly, Hila; Krishna Murthy, Sarath Babu; Vena, Natalie; Povysil, Gundula; Beenken, Andrew; Verbitsky, Miguel; Shril, Shirlee; Lekkerkerker, Iris; Yang, Sandy; Khan, Atlas; Fasel, David; Wongboonsin, Janewit; Martino, Jeremiah; Ke, Juntao; Elefant, Naama; Tomar, Nikita; Harnof, Ofek; Kisselev, Sergey; Bheda, Shiraz; Reytan-Miron, Sivan; Lim, Tze Y; Jamry-Dziurla, Anna; Lugani, Francesca; Zhang, Jun Y; Marasa, Maddalena; Kolupaeva, Victoria; Groopman, Emily E; Jin, Gina; Ghavami, Iman; Stevens, Kelsey O; Coughlin, Arielle C; Kil, Byum Hee; Chatterjee, Debanjana; Bradbury, Drew; Zheng, Jason; Mehl, Karla; Morban, Maria; Reingold, Rachel; Piva, Stacy; Mu, Xueru; Mitrotti, Adele; Szmigielska, Agnieszka; Gliwińska, Aleksandra; Ranghino, Andrea; Bomback, Andrew S; Badenski, Andrzej; Latos-Bielenska, Anna; Capone, Valentina; Materna-Kiryluk, Anna; Amoroso, Antonio; Izzi, Claudia; La Scola, Claudio; Cohen, David Jonathan; Santoro, Domenico; Drozdz, Dorota; Fiaccadori, Enrico; Lin, Fangming; Scolari, Francesco; Tondolo, Francesco; La Manna, Gaetano; Appel, Gerald B; Ghiggeri, Gian Marco; Zaza, Gianluigi; Montini, Giovanni; Masnata, Giuseppe; Krzemien, Grażyna; Pisani, Isabella; Radhakrishnan, Jai; Zachwieja, Katarzyna; Gesualdo, Loreto; Biancone, Luigi; Meneghesso, Davide; Mizerska-Wasiak, Malgorzata; Tkaczyk, Marcin; Zaniew, Marcin; Borszewska-Kornacka, Maria K; Szczepanska, Maria; Saraga, Marijan; Rao, Maya K; Bodria, Monica; Miklaszewska, Monika; Uy, Natalie S; Baraldi, Olga; Bjanid, Omar; Esposito, Pasquale; Zamboli, Pasquale; Marzuillo, Pierluigi; Canetta, Pietro A; Sikora, Przemyslaw; Westland, Rik; Crew, Russell J; Alam, Shumyle; Guarino, Stefano; Negrisolo, Susanna; Hays, Thomas; Mane, Shrikant; Grandinetti, Valeria; Tasic, Velibor; Lozanovski, Vladimir J; Caliskan, Yasar; Goldstein, David; Lifton, Richard P; Ionita-Laza, Iuliana; Kiryluk, Krzysztof; van Eerde, Albertien M; Hildebrandt, Friedhelm; Sanna-Cherchi, Simone; Gharavi, Ali G

Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability

PRMT9基因双等位基因功能缺失变异会导致一种综合征型智力障碍。

Kröll-Hermi, Ariane; Stoetzel, Corinne; Etard, Christelle; Halabelian, Levon; Schaefer, Elise; Scheidecker, Sophie; Kahrizi, Kimia; Payman, Jamali; Geoffroy, Véronique; Prasad, Megana; Obringer, Cathy; Ruch, Laurie; Girard, Amandine; Zeng, Hong; Li, Fengling; Plassard, Damien; Keime, Céline; Mattioli, Francesca; Feger, Claire; Piton, Amélie; Fujita, Atsushi; Matsumoto, Naomichi; Castro, Matheus Augusto Araujo; Ae, Kim Chong; Ruaud, Lyse; Levy, Jonathan; Dozières, Blandine; Tabet, Anne-Claude; Wentzensen, Ingrid M; Santiago-Sim, Teresa; Yusupov, Roman; Tveten, Kristian; Smeland, Marie Falkenberg; Alkhunaizi, Ebba; Cowing, Gina; Li, Chumei; Wortmann, Saskia B; Feichtinger, René G; Mayr, Johannes A; Gonorazky, Herman; Jing, Gan; Wang, Xiaodong; Wang, Jia; Bierhals, Tatjana; Grinstein, Lev; Herget, Theresia; Ruiz, Anna; Gabau, Elisabeth; Kampmeier, Antje; Kassel, Olivier; Kuechler, Alma; Platzer, Konrad; Jamra, Rami Abou; Woerner, Audrey; Idleburg, Michaela; Kircher, Susanne Gerit; Laccone, Franco; Golob, Barbara; Peterlin, Borut; Čuturilo, Goran; Tasic, Velibor; Kolvenbach, Caroline M; Hildebrandt, Friedhelm; Ramos, Luiza L P; Kok, Fernando; Buck, Cecilia Barbosa; van de Laar, Ingrid M B H; de Man, Stella A; Taşdelen, Elifcan; Sezer, Abdullah; Büke, Afife; Yavuz, Zehra; Çomoğlu, Selim Selçuk; Costin, Carrie; Tran Mau Them, Frédéric; Lacaze, Elodie; Courtin, Thomas; Héron, Delphine; Keren, Boris; Whalen, Sandra; Roume, Joelle; Yang, Yanzhong; Hoffer, Mariëtte J V; van Haeringen, Arie; Najmabadi, Hossein; Arrowsmith, Cheryl H; Strähle, Uwe; Dollfus, Hélène; Muller, Jean

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families

三重外显子组测序在19.62%的先天性肾脏和泌尿道畸形(CAKUT)家族中发现了新的候选基因中的新生变异。

Merz, Lea Maria; Kolvenbach, Caroline M; Wang, Chunyan; Mertens, Nils David; Seltzsam, Steve; Mansour, Bshara; Zheng, Bixia; Schneider, Sophia; Schierbaum, Luca; Hölzel, Selina; Salmanullah, Daanya; Pantel, Dalia; Kalkar, Gina; Connaughton, Dervla M; Mann, Nina; Wu, Chen-Han Wilfred; Kause, Franziska; Nakayama, Makiko; Dai, Rufeng; Schneider, Ronen; Buerger, Florian; Nicolas-Frank, Camille; Yousef, Kirollos; Lemberg, Katharina; Saida, Ken; Yu, Seyoung; Elmubarak, Izzeldin; Franken, Gijs A C; Lomjansook, Kraisoon; Braun, Alina; Bauer, Stuart B; Rodig, Nancy M; Somers, Michael J G; Traum, Avram Z; Stein, Deborah R; Daga, Ankana; Baum, Michelle A; Daouk, Ghaleb H; Awad, Hazem S; Eid, Loai A; El Desoky, Sherif; Shalaby, Mohammed A; Kari, Jameela A; Ooda, Said; Fathy, Hanan M; Soliman, Neveen A; Nabhan, Marwa; Abdelrahman, Safaa; Hilger, Alina C; Mane, Shrikant M; Ferguson, Michael A; Tasic, Velibor; Shril, Shirlee; Hildebrandt, Friedhelm

Trio Exome Sequencing in VACTERL Association

VACTERL 关联中的三重外显子组测序

Ćomić, Jasmina; Tilch, Erik; Riedhammer, Korbinian M; Brugger, Melanie; Brunet, Theresa; Eyring, Katharina; Vill, Katharina; Redler, Silke; Tasic, Velibor; Schmiedeke, Eberhard; Schäfer, Frank-Mattias; Abazi-Emini, Nora; Jenetzky, Ekkehart; Schwarzer, Nicole; Widenmann, Anke; Lacher, Martin; Zech, Michael; Grasshoff-Derr, Sabine; Geßner, Michaela; Kabs, Carmen; Seitz, Barbara; Heydweiller, Andreas C; Muensterer, Oliver; Lange-Sperandio, Bärbel; Rolle, Udo; Schumacher, Johannes; Braunisch, Matthias C; Berutti, Riccardo; Reutter, Heiko; Hoefele, Julia

COL4A5-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype

COL4A5-p.Gly624Asp 是欧洲与轻度阿尔波特综合征表型相关的最主要变异体

Krüger, Bastian M; Jens, Annika; Neuhaus, Anna; Ćomić, Jasmina; Berutti, Riccardo; de Fallois, Jonathan; Petzold, Friederike; Münch, Johannes; Kowald, Jan; Lindner, Tom H; Budde, Klemens; Brüning, Klara K; Thumfart, Julia; Haas, Jacob; Brigl, Carolin B; Amann, Kerstin; Tasic, Velibor; Abazi-Emini, Nora; Nushi-Stavileci, Valbona; Putnik, Jovana; Stajić, Nataša; Seelow, Evelyn; Hammett, Charlotte; Eckardt, Kai-Uwe; Riedhammer, Korbinian M; Schrezenmeier, Eva V; Hoefele, Julia; Halbritter, Jan

Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.

人类肾脏和泌尿道先天性异常中茶衫锌指同源框 3 (TSHZ3) 基因的杂合变异

Kesdiren Esra, Martens Helge, Brand Frank, Werfel Lina, Wedekind Lukas, Trowe Mark-Oliver, Schmitz Jessica, Hennies Imke, Geffers Robert, Gucev Zoran, Seeman Tomáš, Schmidt Sonja, Tasic Velibor, Fasano Laurent, Bräsen Jan H, Kispert Andreas, Christians Anne, Haffner Dieter, Weber Ruthild G

Survey of legislative frameworks and national recommendations governing paediatric maintenance haemodialysis in Europe

欧洲儿科维持性血液透析相关立法框架和国家建议调查

Vedrine, Enzo; Schmitt, Claus Peter; Walle, Johan Vande; Shtiza, Diamant; Arbeiter, Klaus; Snauwaert, Evelien; Pokrajac, Danka; Roussinov, Dimitar; Milosevic, Danko; Avraam, Elia; Zieg, Jakub; Schmidt, Ida Maria; Toots, Ylle; Holtta, Tuula; Klaus, Günter; Askiti, Varvara; Tory, Kalman; Sweeney, Clodagh; Verrina, Enrico; Jeruma, Edite; Jankauskiene, Augustina; Conti, Valerie Said; Lutovac, Branko; Koster-Kamphuis, Linda; Tasic, Velibor; Bjerre, Anna Kristina; Szczepańska, Maria; Afonso, Alberto Caldas; Rãchişan, Andreea Liana; Spasojevic, Brankica; Janko, Victor; Novljan, Gregor; Ortega, Pedro J; Sartz, Lisa; Tschumi, Sibylle; Bakkaloglu, Sevcan Azime; Dudley, Jan; Ivanov, Dymtro D; Shroff, Rukshana; Ranchin, Bruno

A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency

罗姆人群体中一种常见的MOCS2变异与一种新型的轻度钼辅因子缺乏症相关。

Cho, Sung Kweon; Schwarz, Guenter; Tasic, Velibor; Křížková, Michaela; Krijt, Jakub; Roeper, Juliane; Honzík, Tomáš; Šebesta, Ivan; Kožich, Viktor; Šaligová, Jana; Pavelcova, Katerina; Masinova, Jana; Winkler, Cheryl A; Stiburkova, Blanka

Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract

开发一种用于预测患有先天性肾脏和泌尿系统畸形的儿童和青少年HNF1B基因突变的工具

Kołbuc, Marcin; Kołek, Mateusz F; Motyka, Rafał; Bieniaś, Beata; Habbig, Sandra; Burgmaier, Kathrin; Prikhodina, Larisa; Papizh, Svetlana; Tasic, Velibor; Okorn, Christine; Szczepańska, Maria; Kiliś-Pstrusińska, Katarzyna; Wasilewska, Anna; Adamczyk, Piotr; Tkaczyk, Marcin; Pańczyk-Tomaszewska, Małgorzata; Miklaszewska, Monika; Pawlaczyk, Krzysztof; Bukowska-Olech, Ewelina; Jamsheer, Aleksander; Jankauskiene, Augustina; König, Jens; Cheong, Hae Il; Ahn, Yo Han; Kaspar, Sophie; Sikora, Przemysław; Beck, Bodo B; Zaniew, Marcin