Wu, Chen-Han Wilfred; Lim, Tze Y.; Wang, Chunyan; Seltzsam, Steve; Zheng, Bixia; Schierbaum, Luca; Schneider, Sophia; Mann, Nina; Connaughton, Dervla M.; Nakayama, Makiko; van der Ven, Amelie T.; Dai, Rufeng; Kolvenbach, Caroline M.; Kause, Franziska; Ottlewski, Isabel; Stajic, Natasa; Soliman, Neveen A.; Kari, Jameela A.; El Desoky, Sherif; Fathy, Hanan M.; Milosevic, Danko; Turudic, Daniel; Al Saffar, Muna; Awad, Hazem S.; Eid, Loai A.; Ramanathan, Aravind; Senguttuvan, Prabha; Mane, Shrikant M.; Lee, Richard S.; Bauer, Stuart B.; Lu, Weining; Hilger, Alina C.; Tasic, Velibor; Shril, Shirlee; Sanna-Cherchi, Simone; Hildebrandt, Friedhelm

PODO: Trial Design: Phase 2 Study of PF-06730512 in Focal Segmental Glomerulosclerosis

PODO: 试验设计: 局灶节段性肾小球硬化PF-06730512的2期研究

KIDNEY INTERNATIONAL REPORTS

IF5.7

2021-06-018

OAAI

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2020-10-0124

OAAI

Connaughton, Dervla M.; Dai, Rufeng; Owen, Danielle J.; Marquez, Jonathan; Mann, Nina; Graham-Paquin, Adda L.; Nakayama, Makiko; Coyaud, Etienne; Laurent, Estelle Mn; St-Germain, Jonathan R.; Blok, Lot Snijders; Vino, Arianna; Klambt, Verena; Deutsch, Konstantin; Wu, Chen-Han Wilfred; Kolvenbach, Caroline M.; Kause, Franziska; Ottlewski, Isabel; Schneider, Ronen; Kitzler, Thomas M.; Majmundar, Amar J.; Buerger, Florian; Onuchic-Whitford, Ana C.; Mao Youying; Kolb, Amy; Salmanullah, Daanya; Chen, Evan; van der Ven, Amelie T.; Rao, Jia; Ityel, Hadas; Seltzsam, Steve; Rieke, Johanna M.; Chen, Jing; Vivante, Asaf; Hwang, Daw-Yang; Kohl, Stefan; Dworschak, Gabriel C.; Hermle, Tobias; Alders, Marielle; Bartolomaeus, Tobias; Bauer, Stuart B.; Baum, Michelle A.; Brilstra, Eva H.; Challman, Thomas D.; Zyskind, Jacob; Costin, Carrie E.; Dipple, Katrina M.; Duijkers, Floor A.; Ferguson, Marcia; Fitzpatrick, David R.; Fick, Roger; Glass, Ian A.; Hulick, Peter J.; Kline, Antonie D.; Krey, Ilona; Kumar, Selvin; Lu, Weining; Marco, Elysa J.; Wentzensen, Ingrid M.; Mefford, Heather C.; Platzer, Konrad; Povolotskaya, Inna S.; Savatt, Juliann M.; Shcherbakova, Natalia, V; Senguttuvan, Prabha; Squire, Audrey E.; Stein, Deborah R.; Thiffault, Isabelle; Voinova, Victoria Y.; Somers, Michael J. G.; Ferguson, Michael A.; Traum, Avram Z.; Daouk, Ghaleb H.; Daga, Ankana; Rodig, Nancy M.; Terhal, Paulien A.; van Binsbergen, Ellen; Eid, Loai A.; Tasic, Velibor; Rasouly, Hila Milo; Lim, Tze Y.; Ahram, Dina F.; Gharavi, Ali G.; Reutter, Heiko M.; Rehm, Heidi L.; MacArthur, Daniel G.; Lek, Monkol; Laricchia, Kristen M.; Lifton, Richard P.; Xu, Hong; Mane, Shrikant M.; Sanna-Cherchi, Simone; Sharrocks, Andrew D.; Raught, Brian; Fisher, Simon E.; Bouchard, Maxime; Khokha, Mustafa K.; Shril, Shirlee; Hildebrandt, Friedhelm

Mycobacterium tuberculosis Beijing genotype strains and unfavourable treatment outcomes: a systematic review and meta-analysis

结核分枝杆菌北京基因型菌株与不良治疗结局的系统评价和meta分析

CLINICAL MICROBIOLOGY AND INFECTION

IF8.5

2020-02-0131

OAAI

Integrin-Linked Kinase Deficiency in Collecting Duct Principal Cell Promotes Necroptosis of Principal Cell and Contributes to Kidney Inflammation and Fibrosis

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

IF9.4

2019-10-2524

OAAI

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

IF9.4

2018-08-24140

OAAI

van der Ven, Amelie T.; Connaughton, Dervla M.; Ityel, Hadas; Mann, Nina; Nakayama, Makiko; Chen, Jing; Vivante, Asaf; Hwang, Daw-yang; Schulz, Julian; Braun, Daniela A.; Schmidt, Johanna Magdalena; Schapiro, David; Schneider, Ronen; Warejko, Jillian K.; Daga, Ankana; Majmundar, Amar J.; Tan, Weizhen; Jobst-Schwan, Tilman; Hermle, Tobias; Widmeier, Eugen; Ashraf, Shazia; Amar, Ali; Hoogstraaten, Charlotte A.; Hugo, Hannah; Kitzler, Thomas M.; Kause, Franziska; Kolvenbach, Caroline M.; Dai, Rufeng; Spaneas, Leslie; Amann, Kassaundra; Stein, Deborah R.; Baum, Michelle A.; Somers, Michael J. G.; Rodig, Nancy M.; Ferguson, Michael A.; Traum, Avram Z.; Daouk, Ghaleb H.; Bogdanovic, Radovan; Stajic, Natasa; Soliman, Neveen A.; Kari, Jameela A.; El Desoky, Sherif; Fathy, Hanan M.; Milosevic, Danko; Al-Saffar, Muna; Awad, Hazem S.; Eid, Loai A.; Selvin, Aravind; Senguttuvan, Prabha; Sanna-Cherchi, Simone; Rehm, Heidi L.; MacArthur, Daniel G.; Lek, Monkol; Laricchia, Kristen M.; Wilson, Michael W.; Mane, Shrikant M.; Lifton, Richard P.; Lee, Richard S.; Bauer, Stuart B.; Lu, Weining; Reutter, Heiko M.; Tasic, Velibor; Shril, Shirlee; Hildebrandt, Friedhelm

Identification of direct negative cross-talk between the SLIT2 and bone morphogenetic protein-Gremlin signaling pathways

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2018-03-0121

OAAI

Blocking peptides and molecular mimicry as treatment for kidney disease

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY

IF3.4

2017-06-017

OAAI

Roundabout receptor 2 maintains inhibitory control of the adult midbrain

ELIFE

IF0

2017-04-1018

A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

IF9.4

2017-04-0538

OAAI

Vivante, Asaf; Mann, Nina; Yonath, Hagith; Weiss, Anna-Carina; Getwan, Maike; Kaminski, Michael M.; Bohnenpoll, Tobias; Teyssier, Catherine; Chen, Jing; Shril, Shirlee; van der Ven, Amelie T.; Ityel, Hadas; Schmidt, Johanna Magdalena; Widmeier, Eugen; Bauer, Stuart B.; Sanna-Cherchi, Simone; Gharavi, Ali G.; Lu, Weining; Magen, Daniella; Shukrun, Rachel; Lifton, Richard P.; Tasic, Velibor; Stanescu, Horia C.; Cavailles, Vincent; Kleta, Robert; Anikster, Yair; Dekel, Benjamin; Kispert, Andreas; Lienkamp, Soeren S.; Hildebrandt, Friedhelm

Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease

间充质来源的肾单位中Zeb2的丢失导致原发性肾小球囊病

KIDNEY INTERNATIONAL

IF12.6

2016-12-0114

OAAI

Lu W

个人简介

教育背景

工作经历

荣誉奖项

研究方向