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Friedhelm Hildebrandt

harvard medical school

108H-index
592Paper Count
3.8WCitation Count
Published Papers 207
Publication Date
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A protein interactome for the last eukaryotic common ancestor illuminates the biochemical basis of modern genetic diseases
errCell Genomics
IF9
err2026-05-27
err0
errOAAI
errRachael M. Cox; Ophelia Papoulas; Shirlee Shril; Chanjae Lee; Tynan P. Gardner; Zoya T. Ansari; Anna M. Battenhouse; Muyoung Lee; Kevin Drew; Claire D. McWhite; David Yang; Janelle C. Leggere; Dannie Durand; Friedhelm Hildebrandt; John B. Wallingford; Edward M. Marcotte
errShare
errSave
How variant discovery redefines genetic prevalence: the case of cystine stone disease
errEuropean Journal of Human Genetics
IF4.6
err2026-04-09
err0
errOAAI
errChen-Han Wilfred Wu; Joshua Chang; Katreya Lovrenert; Donald Bodner; Friedhelm Hildebrandt; Fredrick R. Schumacher
errShare
errSave
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment
errNature Communications
IF15.7
err2025-11-27
err0
errOAAI
errFlorian Buerger; Daanya Salmanullah; Lorrin Liang; Victoria Gauntner; Kavita Krueger; Jiansong Qi; Josee Normand; Vineeta Sharma; Arathi Ranga; Alexander Rubin; David Ball; Sunwoo Hong; Katharina Lemberg; Ken Saida; Lea Maria Merz; Sanja Sever; Biju Issac; Qianyi Ma; Liang Sun; Anja M. Billing; Fatih Demir; Markus M. Rinschen; Björn Reusch; Bodo B. Beck; Sergio Guerrero-Castillo; Alexis C. Gomez; Michelle T. McNulty; Matthew G. Sampson; Mohamed H. Al-Hamed; Mohammed M. Saleh; Mohamed A. Shalaby; Jameela A. Kari; James P. Fawcett; Friedhelm Hildebrandt; Amar J. Majmundar
errShare
errSave
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes
errNature Communications
IF15.7
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
errShare
errSave
PATJ deficiency leads to cystic kidney disease and related ciliopathies
errHuman Genetics and Genomics Advances
IF3.6
err2025-09-09
err0
errOAAI
errDaniel Epting; Daniela A. Braun; Eva Decker; Elisabeth Ott; Tobias Eisenberger; Nadine Bachmann; Pavel Nedvetsky; Michael P. Krahn; Friedhelm Hildebrandt; Carsten Bergmann
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errSave
Exome analysis links kidney malformations to developmental disorders and reveals causal genes
errNature Communications
IF15.7
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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errSave
Genetic Insights Into Nephrolithiasis and Renal Cancer Predisposition: Precision Medicine in Genes, Diagnosis, and Therapy
errSeminars in Nephrology
IF3.5
err2025-07-15
err0
PREAI
errChen-Han Wilfred Wu; Yu-Ren Mike Huang; Hachem Ziadeh; Bor-En Jong; Prapti Dalal; Hsin-Ti Cindy Lin; Amar Majmundar; Yao-Chou Tsai; Adonis Hijaz; Marshall L. Stoller; Michael Romero; Friedhelm Hildebrandt
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errSave
The contribution of de novo coding mutations to meningomyelocele
errNATURE
IF48.5
err2025-03-26
err0
errOAAI
errHa, Yoo-Jin Jiny; Nisal, Ashna; Tang, Isaac; Lee, Chanjae; Jhamb, Ishani; Wallace, Cassidy; Howarth, Robyn; Schroeder, Sarah; Vong, Keng loi; Meave, Naomi; Jiwani, Fiza; Barrows, Chelsea; Lee, Sangmoon; Jiang, Nan; Patel, Arzoo; Bagga, Krisha; Banka, Niyati; Friedman, Liana; Blanco, Francisco A.; Yu, Seyoung; Rhee, Soeun; Jeong, Hui Su; Plutzer, Isaac; Major, Michael B.; Benoit, Beatrice; Pous, Christian; Heffner, Caleb; Kibar, Zoha; Bot, Gyang Markus; Northrup, Hope; Au, Kit Sing; Strain, Madison; Ashley-Koch, Allison E.; Finnell, Richard H.; Le, Joan T.; Meltzer, Hal S.; Araujo, Camila; Machado, Helio R.; Stevenson, Roger E.; Yurrita, Anna; Mumtaz, Sara; Ahmed, Awais; Khara, Mulazim Hussain; Mutchinick, Osvaldo M.; Medina-Bereciartu, Jose Ramon; Hildebrandt, Friedhelm; Melikishvili, Gia; Marwan, Ahmed I.; Capra, Valeria; Noureldeen, Mahmoud M.; Salem, Aida M. S.; Issa, Mahmoud Y.; Zaki, Maha S.; Xu, Libin; Lee, Ji Eun; Shin, Donghyuk; Alkelai, Anna; Shuldiner, Alan R.; Kingsmore, Stephen F.; Murray, Stephen A.; Gee, Heon Yung; Miller, W. Todd; Tolias, Kimberley F.; Wallingford, John B.; Kim, Sangwoo; Spina Bifida Sequencing Consortium, Joan T.; Koch, Allison E. Ashley; Lupo, Philip J.; Magana, Tony; Kolvenbach, Caroline M.; Shril, Shirlee; Takahashi, Yukitoshi; Salimi-Dafsari, Hormos; Hanak, Brian; Kara, Bulent; Gunes, Ayfer Sakarya; Gonda, David D.; Kirmani, Salman; Tkemaladze, Tinatin
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Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome
errGENES & DISEASES
IF9.4
err2025-03-01
err1
errOAAI
errSchneider, Ronen; Shril, Shirlee; Buerger, Florian; Deutsch, Konstantin; Yousef, Kirollos; Frank, Camille N.; Onuchic-Whitford, Ana C.; Kitzler, Thomas M.; Mao, Youying; Klaembt, Verena; Zahoor, Muhammad Y.; Lemberg, Katharina; Majmundar, Amar J.; Mansour, Bshara; Saida, Ken; Seltzsam, Steve; Kolvenbach, Caroline M.; Merz, Lea Maria; Mertens, Nils D.; Hermle, Tobias; Mann, Nina; Pantel, Dalia; Halawi, Abdul A.; Bao, Aaron; Schierbaum, Luca; Schneider, Sophia; Salmanullah, Daanya; Ben-Dov, Iddo Z.; Sagiv, Itamar; Eid, Loai A.; Awad, Hazem Subhi H.; Al Saffar, Muna; Soliman, Neveen A.; Nabhan, Marwa M.; Kari, Jameela A.; El Desoky, Sherif; Shalaby, Mohamed A.; Ooda, Said; Fathy, Hanan M.; Mane, Shrikant; Lifton, Richard P.; Somers, Michael J. G.; Hildebrandt, Friedhelm
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Epigenomic and phenotypic characterization of DEGCAGS syndrome
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-10-19
err1
PREAI
errKarimi, Karim; Weis, Denisa; Aukrust, Ingvild; Hsieh, Tzung-Chien; Horackova, Marie; Paulsen, Julie; Mendoza Londono, Roberto; Dupuis, Lucie; Dickson, Megan; Lesman, Hellen; Lau, Tracy; Murphy, David; Hama Salih, Khalid; Al-Musawi, Bassam M. S.; Al-Obaidi, Ruqayah G. Y.; Rydzanicz, Malgorzata; Biela, Mateus; Santos, Mafalda Saraiva; Aldeeri, Abdulrahman; Gazda, Hanna T.; Pais, Lynn; Shril, Shirlee; Dollner, Henrik; Bartakke, Sandip; Laccone, Franco; Soltysova, Andrea; Kitzler, Thomas; Soliman, Neveen A.; Relator, Raissa; Levy, Michael A.; Kerkhof, Jennifer; Rzasa, Jessica; Houlden, Henry; Pilshofer, Gabriela V.; Jobst-Schwan, Tilman; Hildebrandt, Friedhelm; Sousa, Sergio B.; Maroofian, Reza; Yu, Timothy W.; Krawitz, Peter; Sadikovic, Bekim; Douzgou Houge, Sofia
errShare
errSave
Genome Sequencing for Diagnosing Rare Diseases
errNEW ENGLAND JOURNAL OF MEDICINE
IF78.5
err2024-06-06
err10
PREAI
errWojcik, Monica H.; Lemire, Gabrielle; Berger, Eva; Zaki, Maha S.; Wissmann, Mariel; Win, Wathone; White, Susan M.; Weisburd, Ben; Wieczorek, Dagmar; Waddell, Leigh B.; Verboon, Jeffrey M.; VanNoy, Grace E.; Toepf, Ana; Tan, Tiong Yang; Syrbe, Steffen; Strehlow, Vincent; Straub, Volker; Stenton, Sarah L.; Snow, Hana; Singer-Berk, Moriel; Silver, Josh; Shril, Shirlee; Seaby, Eleanor G.; Schneider, Ronen; Sankaran, Vijay G.; Sanchis-Juan, Alba; Russell, Kathryn A.; Reinson, Karit; Ravenscroft, Gianina; Radtke, Maximilian; Popp, Denny; Polster, Tilman; Platzer, Konrad; Pierce, Eric A.; Place, Emily M.; Pajusalu, Sander; Pais, Lynn; Ounap, Katrin; Osei-Owusu, Ikeoluwa; Opperman, Henry; Okur, Volkan; Oja, Kaisa Teele; O'Leary, Melanie; O'Heir, Emily; Morel, Chantal F.; Merkenschlager, Andreas; Marchant, Rhett G.; Mangilog, Brian E.; Madden, Jill A.; MacArthur, Daniel; Lovgren, Alysia; Lerner-Ellis, Jordan P.; Lin, Jasmine; Laing, Nigel; Hildebrandt, Friedhelm; Hentschel, Julia; Groopman, Emily; Goodrich, Julia; Gleeson, Joseph G.; Ghaoui, Roula; Genetti, Casie A.; Gburek-Augustat, Janina; Gazda, Hanna T.; Ganesh, Vijay S.; Ganapathi, Mythily; Gallacher, Lyndon; Fu, Jack M.; Evangelista, Emily; England, Eleina; Donkervoort, Sandra; DiTroia, Stephanie; Cooper, Sandra T.; Chung, Wendy K.; Christodoulou, John; Chao, Katherine R.; Cato, Liam D.; Bujakowska, Kinga M.; Bryen, Samantha J.; Brand, Harrison; Boennemann, Carsten G.; Beggs, Alan H.; Baxter, Samantha M.; Bartolomaeus, Tobias; Agrawal, Pankaj B.; Talkowski, Michael; Austin-Tse, Christina; Abou Jamra, Rami; Rehm, Heidi L.; O'Donnell-Luria, Anne
errShare
errSave
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2024-05-01
err7
errOAAI
errLemire, Gabrielle; Sanchis-Juan, Alba; Russell, Kathryn; Baxter, Samantha; Chao, Katherine R.; Singer-Berk, Moriel; Groopman, Emily; Wong, Isaac; England, Eleina; Goodrich, Julia; Pais, Lynn; Austin-Tse, Christina; DiTroia, Stephanie; O'Heir, Emily; Ganesh, Vijay S.; Wojcik, Monica H.; Evangelista, Emily; Snow, Hana; Osei-Owusu, Ikeoluwa; Fu, Jack; Singh, Mugdha; Mostovoy, Yulia; Huang, Steve; Garimella, Kiran; Kirkham, Samantha L.; Neil, Jennifer E.; Shao, Diane D.; Walsh, Christopher A.; Argilli, Emanuela; Le, Carolyn; Sherr, Elliott H.; Gleeson, Joseph G.; Shril, Shirlee; Schneider, Ronen; Hildebrandt, Friedhelm; Sankaran, Vijay G.; Madden, Jill A.; Genetti, Casie A.; Beggs, Alan H.; Agrawal, Pankaj B.; Bujakowska, Kinga M.; Place, Emily; Pierce, Eric A.; Donkervoort, Sandra; Boennemann, Carsten G.; Gallacher, Lyndon; Stark, Zornitza; Tan, Tiong Yang; White, Susan M.; Toepf, Ana; Straub, Volker; Fleming, Mark D.; Pollak, Martin R.; Ounap, Katrin; Pajusalu, Sander; Donald, Kirsten A.; Bruwer, Zandre; Ravenscroft, Gianina; Laing, Nigel G.; MacArthur, Daniel G.; Rehm, Heidi L.; Talkowski, Michael E.; Brand, Harrison; O'Donnell-Luria, Anne
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Quantitative phenotyping of Nphs1 knockout mice as a prerequisite for gene replacement studies
errAMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
IF3.4
err2024-05-01
err0
PREAI
errBuerger, Florian; Merz, Lea M.; Saida, Ken; Yu, Seyoung; Salmanullah, Daanya; Lemberg, Katharina; Mertens, Nils D.; Mansour, Bshara; Kolvenbach, Caroline M.; Yousef, Kirollos; Hoelzel, Selina; Braun, Alina; Franken, Gijs A. C.; Goncalves, Kevin A.; Steinsapir, Andrew; Endlich, Nicole; Schneider, Ronen; Shril, Shirlee; Hildebrandt, Friedhelm
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errSave
The evolving landscape of monogenic nephrolithiasis and therapeutic innovations
errNATURE REVIEWS UROLOGY
IF14.6
err2024-04-17
err0
PREAI
errWu, Chen-Han Wilfred; Huang, Yu-Ren; Bodner, Donald; Schumacher, Fredrick R.; Baum, Michelle; Hildebrandt, Friedhelm
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Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
errKIDNEY INTERNATIONAL
IF12.6
err2024-04-01
err0
errOAAI
errRiedhammer, Korbinian M.; Nguyen, Thanh-Minh T.; Kosukcu, Can; Calzada-Wack, Julia; Li, Yong; Batzir, Nurit Assia; Saygili, Seha; Wimmers, Vera; Kim, Gwang-Jin; Chrysanthou, Marialena; Bakey, Zeineb; Sofrin-Drucker, Efrat; Kraiger, Markus; Sanz-Moreno, Adrian; Amarie, Oana V.; Rathkolb, Birgit; Klein-Rodewald, Tanja; Garrett, Lillian; Hoelter, Sabine M.; Seisenberger, Claudia; Haug, Stefan; Schlosser, Pascal; Marschall, Susan; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Wuttke, Matthias; de Angelis, Martin Hrabe; Comic, Jasmina; Dogan, Ozlem Akgun; Ozluk, Yasemin; Tasdemir, Mehmet; Agbas, Ayse; Canpolat, Nur; Orenstein, Naama; Caliskan, Salim; Weber, Ruthild G.; Bergmann, Carsten; Jeanpierre, Cecile; Saunier, Sophie; Lim, Tze Y.; Hildebrandt, Friedhelm; Alhaddad, Bader; Basel-Salmon, Lina; Borovitz, Yael; Wu, Kaman; Antony, Dinu; Matschkal, Julia; Schaaf, Christian W.; Renders, Lutz; Schmaderer, Christoph; Rogg, Manuel; Schell, Christoph; Meitinger, Thomas; Heemann, Uwe; Koettgen, Anna; Arnold, Sebastian J.; Ozaltin, Fatih; Schmidts, Miriam; Hoefele, Julia
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Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
errNATURE COMMUNICATIONS
IF15.7
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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The genetics and pathogenesis of CAKUT
errNATURE REVIEWS NEPHROLOGY
IF39.8
err2023-07-31
err20
PREAI
errKolvenbach, Caroline M.; Shril, Shirlee; Hildebrandt, Friedhelm
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LRRC6 regulates biogenesis of motile cilia by aiding FOXJ1 translocation into the nucleus
errCELL COMMUNICATION AND SIGNALING
IF8.9
err2023-06-16
err7
errOAAI
errKim, Dong Yun; Sub, Yu Jin; Kim, Hye-Youn; Cho, Kyeong Jee; Choi, Won Il; Choi, Yo Jun; Lee, Min Goo; Hildebrandt, Friedhelm; Gee, Heon Yung
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errSave
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
errNATURE COMMUNICATIONS
IF15.7
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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Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes
errFRONTIERS IN MEDICINE
IF3
err2023-03-23
err5
errOAAI
errYu, Seyoung; Choi, Yo Jun; Rim, John Hoon; Kim, Hye-Youn; Bekheirnia, Nasim; Swartz, Sarah Jane; Dai, Hongzheng; Gu, Shen Linda; Lee, Soyeon; Nishinakamura, Ryuichi; Hildebrandt, Friedhelm; Bekheirnia, Mir Reza; Gee, Heon Yung
errShare
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Research Directions

No research directions
Co-authors
Cooperation Journals
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Jay Shendure
H-index: 167 · Papers: 662
R
Richard P. Lifton
H-index: 150 · Papers: 571
E
Eamonn R. Maher
H-index: 134 · Papers: 850
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