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Rik Westland

amsterdam university medical center

26H指数
73论文数
2.5K被引数
收录论文 33
发表时间
Whole-genome sequencing characterizes monogenic and polygenic contributions to structural kidney and urinary tract malformations全基因组测序揭示单基因和多基因对结构性肾脏和尿路畸形的影响
err2026-09-21
err0
errOAAI
errMelanie M.Y. Chan; Omid Sadeghi-Alavijeh; Seth du Preez; Catalin D. Voinescu; Loes F.M. van der Zanden; Sander Groen in ’t Woud; Michiel F. Schreuder; Wout Feitz; Enrico Mingardo; Alina C. Hilger; Heiko Reutter; Lisanne M. Vendrig; Rik Westland; Glenda M. Beaman; William G. Newman; Adrian S. Woolf; Horia C. Stanescu; Adam P. Levine; Detlef Böckenhauer; Daniel P. Gale
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APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tract先天性肾脏和尿路异常儿童的APOL1肾脏风险变异和结局
err2026-01-14
err0
PREAI
errLisanne M. Vendrig; Juntao Ke; Michael W. T. Tanck; Tze Y. Lim; Elena Martinelli; Monica Bodria; Valentina Capone; Claudia Izzi; Claudio La Scola; Umberto Maggiore; Pierluigi Marzuillo; Giuseppe Masnata; Frank D. Mentch; Giovanni Montini; Isabella Pisani; Huiqi Qu; Matthew G. Sampson; Ana Cristina Simões-e-Silva; Alexandria Thomas; Jaap W. Groothoff; Hakon Hakonarson; Gian Marco Ghiggeri; Miguel Verbitsky; Elena N. Levtchenko; Simone Sanna-Cherchi; Rik Westland
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Dissecting Normal and Abnormal Human Kidney Development Using Multiomics利用多组学方法解析正常与异常人类肾脏发育
err2025-11-01
err1
PREAI
errKlomp, Luna S.; Mavrommatis, Lampros; Arcolino, Fanny O.; Lantermans, Hildo C.; Levtchenko, Elena; Kuppe, Christoph; Westland, Rik
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Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes作者更正:外显子分析将肾脏畸形与发育障碍联系起来,并揭示了因果基因
err2025-10-09
err0
errOAAI
errHila Milo Rasouly; Sarath Babu Krishna Murthy; Natalie Vena; Gundula Povysil; Andrew Beenken; Miguel Verbitsky; Shirlee Shril; Iris Lekkerkerker; Sandy Yang; Atlas Khan; David Fasel; Janewit Wongboonsin; Jeremiah Martino; Juntao Ke; Naama Elefant; Nikita Tomar; Ofek Harnof; Sergey Kisselev; Shiraz Bheda; Sivan Reytan-Miron; Tze Y. Lim; Anna Jamry-Dziurla; Francesca Lugani; Jun Y. Zhang; Maddalena Marasa; Victoria Kolupaeva; Emily E. Groopman; Gina Jin; Iman Ghavami; Kelsey O. Stevens; Arielle C. Coughlin; Byum Hee Kil; Debanjana Chatterjee; Drew Bradbury; Jason Zheng; Karla Mehl; Maria Morban; Rachel Reingold; Stacy Piva; Xueru Mu; Adele Mitrotti; Agnieszka Szmigielska; Aleksandra Gliwińska; Andrea Ranghino; Andrew S. Bomback; Andrzej Badenski; Anna Latos-Bielenska; Valentina Capone; Anna Materna-Kiryluk; Antonio Amoroso; Claudia Izzi; Claudio La Scola; David Jonathan Cohen; Domenico Santoro; Dorota Drozdz; Enrico Fiaccadori; Fangming Lin; Francesco Scolari; Francesco Tondolo; Gaetano La Manna; Gerald B. Appel; Gian Marco Ghiggeri; Gianluigi Zaza; Giovanni Montini; Giuseppe Masnata; Grażyna Krzemien; Isabella Pisani; Jai Radhakrishnan; Katarzyna Zachwieja; Loreto Gesualdo; Luigi Biancone; Davide Meneghesso; Malgorzata Mizerska-Wasiak; Marcin Tkaczyk; Marcin Zaniew; Maria K. Borszewska-Kornacka; Maria Szczepanska; Marijan Saraga; Maya K. Rao; Monica Bodria; Monika Miklaszewska; Natalie S. Uy; Olga Baraldi; Omar Bjanid; Pasquale Esposito; Pasquale Zamboli; Pierluigi Marzuillo; Pietro A. Canetta; Przemyslaw Sikora; Rik Westland; Russell J. Crew; Shumyle Alam; Stefano Guarino; Susanna Negrisolo; Thomas Hays; Shrikant Mane; Valeria Grandinetti; Velibor Tasic; Vladimir J. Lozanovski; Yasar Caliskan; David Goldstein; Richard P. Lifton; Iuliana Ionita-Laza; Krzysztof Kiryluk; Albertien M. van Eerde; Friedhelm Hildebrandt; Simone Sanna-Cherchi; Ali G. Gharavi
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Exome analysis links kidney malformations to developmental disorders and reveals causal genes外显子分析将肾脏畸形与发育障碍联系起来,并揭示了致病基因
err2025-08-07
err0
errOAAI
errHila Milo Rasouly; Sarath Babu Krishna Murthy; Natalie Vena; Gundula Povysil; Andrew Beenken; Miguel Verbitsky; Shirlee Shril; Iris Lekkerkerker; Sandy Yang; Atlas Khan; David Fasel; Janewit Wongboonsin; Jeremiah Martino; Juntao Ke; Naama Elefant; Nikita Tomar; Ofek Harnof; Sergey Kisselev; Shiraz Bheda; Sivan Reytan-Miron; Tze Y. Lim; Anna Jamry-Dziurla; Francesca Lugani; Jun Y. Zhang; Maddalena Marasa; Victoria Kolupaeva; Emily E. Groopman; Gina Jin; Iman Ghavami; Kelsey O. Stevens; Arielle C. Coughlin; Byum Hee Kil; Debanjana Chatterjee; Drew Bradbury; Jason Zheng; Karla Mehl; Maria Morban; Rachel Reingold; Stacy Piva; Xueru Mu; Adele Mittrori; Agnieszka Szmigielska; Aleksandra Gliwińska; Andrea Ranghino; Andrew S. Bomback; Andrzej Badenski; Anna Latos-Bielenska; Valentina Capone; Anna Materna-Kiryluk; Antonio Amoroso; Claudia Izzi; Claudio La Scola; David Jonathan Cohen; Domenico Santoro; Dorota Drozdz; Enrico Fiaccadori; Fangming Lin; Francesco Scolari; Francesco Tondolo; Gaetano La Manna; Gerald B. Appel; Gian Marco Ghiggeri; Gianluigi Zaza; Giovanni Montini; Giuseppe Masnata; Grażyna Krzemien; Isabella Pisani; Jai Radhakrishnan; Katarzyna Zachwieja; Loreto Gesualdo; Luigi Biancone; Davide Meneghesso; Malgorzata Mizerska-Wasiak; Marcin Tkaczyk; Marcin Zaniew; Maria K. Borszewska-Kornacka; Maria Szczepanska; Marijan Saraga; Maya K. Rao; Monica Bodria; Monika Miklaszewska; Natalie S. Uy; Olga Baraldi; Omar Bjanid; Pasquale Esposito; Pasquale Zamboli; Pierluigi Marzuillo; Pietro A. Canetta; Przemyslaw Sikora; Rik Westland; Russell J. Crew; Shumyle Alam; Stefano Guarino; Susanna Negrisolo; Thomas Hays; Shrikant Mane; Valeria Grandinetti; Velibor Tasic; Vladimir J. Lozanovski; Yasar Caliskan; David Goldstein; Richard P. Lifton; Iuliana Ionita-Laza; Krzysztof Kiryluk; Albertien M. van Eerde; Friedhelm Hildebrandt; Simone Sanna-Cherchi; Ali G. Gharavi
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Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet)ChatGPT在告知罕见肾脏病患者及家属方面的风险与益处:欧洲罕见肾脏病参考网络(ERKNet)的探索性评估
err2025-04-16
err0
errOAAI
errvan Eerde, Albertien M.; Teixeira, Ana; Galletti, Flavia; Maternik, Michal; Capone, Valentina; Westland, Rik; Mulder, Jaap; Osterholt, Thomas; Neukel, Valentina; Weber, Lutz T.; Liebau, Max C.; Schaefer, Franz; Kohl, Stefan
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Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies
err2023-12-01
err1
errOAAI
errMartino, Jeremiah; Liu, Qingxue; Vukojevic, Katarina; Ke, Juntao; Lim, Tze Y.; Khan, Atlas; Gupta, Yask; Perez, Alejandra; Yan, Zonghai; Rasouly, Hila Milo; Vena, Natalie; Lippa, Natalie; Giordano, Jessica L.; Saraga, Marijan; Saraga-Babic, Mirna; Westland, Rik; Bodria, Monica; Piaggio, Giorgio; Bendapudi, Pavan K.; Iglesias, Alejandro D.; Wapner, Ronald J.; Tasic, Velibo; Wang, Fan; Ionita-Laza, Iuliana; Ghiggeri, Gian Marco; Kiryluk, Krzysztof; Sampogna, Rosemary, V; Mendelsohn, Cathy L.; D'Agati, Vivette D.; Gharavi, Ali G.; Sanna-Cherchi, Simone
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Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
err2023-11-30
err17
errOAAI
errGupta, Yask; Friedman, David J.; McNulty, Michelle T.; Khan, Atlas; Lane, Brandon; Wang, Chen; Ke, Juntao; Jin, Gina; Wooden, Benjamin; Knob, Andrea L.; Lim, Tze Y.; Appel, Gerald B.; Huggins, Kinsie; Liu, Lili; Mitrotti, Adele; Stangl, Megan C.; Bomback, Andrew; Westland, Rik; Bodria, Monica; Marasa, Maddalena; Shang, Ning; Cohen, David J.; Crew, Russell J.; Morello, William; Canetta, Pietro; Radhakrishnan, Jai; Martino, Jeremiah; Liu, Qingxue; Chung, Wendy K.; Espinoza, Angelica; Luo, Yuan; Wei, Wei-Qi; Feng, Qiping; Weng, Chunhua; Fang, Yilu; Kullo, Iftikhar J.; Naderian, Mohammadreza; Limdi, Nita; Irvin, Marguerite R.; Tiwari, Hemant; Mohan, Sumit; Rao, Maya; Dube, Geoffrey K.; Chaudhary, Ninad S.; Gutierrez, Orlando M.; Judd, Suzanne E.; Cushman, Mary; Lange, Leslie A.; Lange, Ethan M.; Bivona, Daniel L.; Verbitsky, Miguel; Winkler, Cheryl A.; Kopp, Jeffrey B.; Santoriello, Dominick; Batal, Ibrahim; Pinheiro, Sergio Veloso Brant; Oliveira, Eduardo Araujo; Simoes e Silva, Ana Cristina; Pisani, Isabella; Fiaccadori, Enrico; Lin, Fangming; Gesualdo, Loreto; Amoroso, Antonio; Ghiggeri, Gian Marco; D'Agati, Vivette D.; Magistroni, Riccardo; Kenny, Eimear E.; Loos, Ruth J. F.; Montini, Giovanni; Hildebrandt, Friedhelm; Paul, Dirk S.; Petrovski, Slave; Goldstein, David B.; Kretzler, Matthias; Gbadegesin, Rasheed; Gharavi, Ali G.; Kiryluk, Krzysztof; Sampson, Matthew G.; Pollak, Martin R.; Sanna-Cherchi, Simone
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Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome多种群全基因组关联研究表明免疫和非免疫因素与儿童激素敏感型肾病综合征有关
err2023-04-29
err17
errOAAI
errBarry, Alexandra; McNulty, Michelle T.; Jia, Xiaoyuan; Gupta, Yask; Debiec, Hanna; Luo, Yang; Nagano, China; Horinouchi, Tomoko; Jung, Seulgi; Colucci, Manuela; Ahram, Dina F.; Mitrotti, Adele; Sinha, Aditi; Teeninga, Nynke; Jin, Gina; Shril, Shirlee; Caridi, Gianluca; Bodria, Monica; Lim, Tze Y.; Westland, Rik; Zanoni, Francesca; Marasa, Maddalena; Turudic, Daniel; Giordano, Mario; Gesualdo, Loreto; Magistroni, Riccardo; Pisani, Isabella; Fiaccadori, Enrico; Reiterova, Jana; Maringhini, Silvio; Morello, William; Montini, Giovanni; Weng, Patricia L.; Scolari, Francesco; Saraga, Marijan; Tasic, Velibor; Santoro, Domenica; van Wijk, Joanna A. E.; Milosevic, Danko; Kawai, Yosuke; Kiryluk, Krzysztof; Pollak, Martin R.; Gharavi, Ali; Lin, Fangmin; Simoes e Silva, Ana Cristina; Loos, Ruth J. F.; Kenny, Eimear E.; Schreuder, Michiel F.; Zurowska, Aleksandra; Dossier, Claire; Ariceta, Gema; Drozynska-Duklas, Magdalena; Hogan, Julien; Jankauskiene, Augustina; Hildebrandt, Friedhelm; Prikhodina, Larisa; Song, Kyuyoung; Bagga, Arvind; Cheong, Hae, II; Ghiggeri, Gian Marco; Vachvanichsanong, Prayong; Nozu, Kandai; Lee, Dongwon; Vivarelli, Marina; Raychaudhuri, Soumya; Tokunaga, Katsushi; Sanna-Cherchi, Simone; Ronco, Pierre; Iijima, Kazumoto; Sampson, Matthew G.
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Uncovering risk factors for kidney injury in children with a solitary functioning kidney
err2023-01-01
err16
errOAAI
errWoud, Sander Groen in't; Roeleveld, Nel; Westland, Rik; Renkema, Kirsten Y.; Steffens, Martijn G.; Gracchi, Valentina; Lilien, Marc R.; van Wijk, Joanna A. E.; Feitz, Wout F. J.; Schreuder, Michiel F.; van der Zanden, Loes F. M.
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A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney
err2022-11-23
err3
errOAAI
errin't Woud, Sander Groen; Maj, Carlo; Renkema, Kirsten Y.; Westland, Rik; Galesloot, Tessel; van Rooij, Iris A. L. M.; Vermeulen, Sita H.; Feitz, Wout F. J.; Roeleveld, Nel; Schreuder, Michiel F.; van der Zanden, Loes F. M.; SOFIA Study Grp
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Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations
err2022-03-01
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errOAAI
errKhan, Kamal; Ahram, Dina F.; Liu, Yangfan P.; Westland, Rik; Sampogna, Rosemary, V; Katsanis, Nicholas; Davis, Erica E.; Sanna-Cherchi, Simone
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Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
err2021-03-01
err30
errOAAI
errIn't Woud, Sander Groen; Westland, Rik; Feitz, Wout F. J.; Roeleveld, Nel; van Wijk, Joanna A. E.; van der Zanden, Loes F. M.; Schreuder, Michiel F.
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The copy number variation landscape of congenital anomalies of the kidney and urinary tract (vol 51, pg 117, 2018)
err2019-02-27
err4
errOAAI
errVerbitsky, Miguel; Westland, Rik; Perez, Alejandra; Kiryluk, Krzysztof; Liu, Qingxue; Krithivasan, Priya; Mitrotti, Adele; Fasel, David A.; Batourina, Ekaterina; Sampson, Matthew G.; Bodria, Monica; Werth, Max; Kao, Charlly; Martino, Jeremiah; Capone, Valentina P.; Vivante, Asaf; Shril, Shirlee; Kil, Byum Hee; Marasa, Maddalena; Zhang, Jun Y.; Na, Young-Ji; Lim, Tze Y.; Ahram, Dina; Weng, Patricia L.; Heinzen, Erin L.; Carrea, Alba; Piaggio, Giorgio; Gesualdo, Loreto; Manca, Valeria; Masnata, Giuseppe; Gigante, Maddalena; Cusi, Daniele; Izzi, Claudia; Scolari, Francesco; van Wijk, Joanna A. E.; Saraga, Marijan; Santoro, Domenico; Conti, Giovanni; Zamboli, Pasquale; White, Hope; Drozdz, Dorota; Zachwieja, Katarzyna; Miklaszewska, Monika; Tkaczyk, Marcin; Tomczyk, Daria; Krakowska, Anna; Sikora, Przemyslaw; Jarmolinski, Tomasz; Borszewska-Kornacka, Maria K.; Pawluch, Robert; Szczepanska, Maria; Adamczyk, Piotr; Mizerska-Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Dobson, Mark G.; Darlow, John M.; Puri, Prem; Barton, David E.; Furth, Susan L.; Warady, Bradley A.; Gucev, Zoran; Lozanovski, Vladimir J.; Tasic, Velibor; Pisani, Isabella; Allegri, Landino; Rodas, Lida M.; Campistol, Josep M.; Jeanpierre, Cecile; Alam, Shumyle; Casale, Pasquale; Wong, Craig S.; Lin, Fangming; Miranda, Debora M.; Oliveira, Eduardo A.; Simoes-e-Silva, Ana Cristina; Barasch, Jonathan M.; Levy, Brynn; Wu, Nan; Hildebrandt, Friedhelm; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Materna-Kiryluk, Anna; Zhang, Feng; Hakonarson, Hakon; Papaioannou, Virginia E.; Mendelsohn, Cathy L.; Gharavi, Ali G.; Sanna-Cherchi, Simone
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The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing
err2019-01-01
err57
PREAI
errRasouly, Hila Milo; Groopman, Emily E.; Heyman-Kantor, Reuben; Fasel, David A.; Mitrotti, Adele; Westland, Rik; Bier, Louise; Weng, Chunhua; Ren, Zhong; Copeland, Brett; Krithivasan, Priya; Chung, Wendy K.; Sanna-Cherchi, Simone; Goldstein, David B.; Gharavi, Ali G.
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The copy number variation landscape of congenital anomalies of the kidney and urinary tract
err2018-12-21
err151
errOAAI
errVerbitsky, Miguel; Westland, Rik; Perez, Alejandra; Kiryluk, Krzysztof; Liu, Qingxue; Krithivasan, Priya; Mitrotti, Adele; Fasel, David A.; Batourina, Ekaterina; Sampson, Matthew G.; Bodria, Monica; Werth, Max; Kao, Charlly; Martino, Jeremiah; Capone, Valentina P.; Vivante, Asaf; Shril, Shirlee; Kil, Byum Hee; Marasa, Maddalena; Zhang, Jun Y.; Na, Young-Ji; Lim, Tze Y.; Ahram, Dina; Weng, Patricia L.; Heinzen, Erin L.; Carrea, Alba; Piaggio, Giorgio; Gesualdo, Loreto; Manca, Valeria; Masnata, Giuseppe; Gigante, Maddalena; Cusi, Daniele; Izzi, Claudia; Scolari, Francesco; van Wijk, Joanna A. E.; Saraga, Marijan; Santoro, Domenico; Conti, Giovanni; Zamboli, Pasquale; White, Hope; Drozdz, Dorota; Zachwieja, Katarzyna; Miklaszewska, Monika; Tkaczyk, Marcin; Tomczyk, Daria; Krakowska, Anna; Sikora, Przemyslaw; Jarmolinski, Tomasz; Borszewska-Kornacka, Maria K.; Pawluch, Robert; Szczepanska, Maria; Adamczyk, Piotr; Mizerska-Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Dobson, Mark G.; Darlow, John M.; Puri, Prem; Barton, David E.; Furth, Susan L.; Warady, Bradley A.; Gucev, Zoran; Lozanovski, Vladimir J.; Tasic, Velibor; Pisani, Isabella; Allegri, Landino; Rodas, Lida M.; Campistol, Josep M.; Jeanpierre, Cecile; Alam, Shumyle; Casale, Pasquale; Wong, Craig S.; Lin, Fangming; Miranda, Debora M.; Oliveira, Eduardo A.; Simoes-e-Silva, Ana Cristina; Barasch, Jonathan M.; Levy, Brynn; Wu, Nan; Hildebrandt, Friedhelm; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Materna-Kiryluk, Anna; Zhang, Feng; Hakonarson, Hakon; Papaioannou, Virginia E.; Mendelsohn, Cathy L.; Gharavi, Ali G.; Sanna-Cherchi, Simone
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