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D

David B. Goldstein

university of california los angeles

116H-index
589Paper Count
7.0WCitation Count
Published Papers 220
Publication Date
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Small molecule inhibition rescues the skeletal dysplasia phenotype ofTrpv4 mutant mice
errJCI Insight
IF6.1
err2026-01-23
err0
PREAI
errNevarez, Lisette; Ismaili, Taylor K.; Zieba, Jennifer; Martin, Jorge; Wachtell, Davis; Diaz, Derick; Ramirez, Jocelyn A.; Aceves, Valeria; Ito, Joshua; Gray, Ryan S.; Goldstein, David; Sahdeo, Sunil; Krakow, Deborah; Cohn, Daniel H.
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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
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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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The diagnostic yield of exome sequencing in liver diseases from a curated gene panel
errSCIENTIFIC REPORTS
IF3.9
err2023-12-06
err2
errOAAI
errKong, Xiao-Fei; Bogyo, Kelsie; Kapoor, Sheena; Shea, Patrick R.; Groopman, Emily E.; Thomas-Wilson, Amanda; Cocchi, Enrico; Milo Rasouly, Hila; Zheng, Beishi; Sun, Siming; Zhang, Junying; Martinez, Mercedes; Vittorio, Jennifer M.; Dove, Lorna M.; Marasa, Maddalena; Wang, Timothy C.; Verna, Elizabeth C.; Worman, Howard J.; Gharavi, Ali G.; Goldstein, David B.; Wattacheril, Julia
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errSave
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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Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency
errPLOS GENETICS
IF3.7
err2023-10-02
err3
errOAAI
errDugger, Sarah A.; Dhindsa, Ryan S.; Sampaio, Gabriela De Almeida; Ressler, Andrew K.; Rafikian, Elizabeth E.; Petri, Sabrina; Letts, Verity A.; Teoh, Jiajie; Ye, Junqiang; Colombo, Sophie; Peng, Yueqing; Yang, Mu; Boland, Michael J.; Frankel, Wayne N.; Goldstein, David B.
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Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor
errFRONTIERS IN CELLULAR NEUROSCIENCE
IF4
err2023-05-18
err6
errOAAI
errColombo, Sophie; Reddy, Haritha P.; Petri, Sabrina; Williams, Damian J.; Shalomov, Boris; Dhindsa, Ryan S.; Gelfman, Sahar; Krizay, Daniel; Bera, Amal K.; Yang, Mu; Peng, Yueqing; Makinson, Christopher D.; Boland, Michael J.; Frankel, Wayne N.; Goldstein, David B.; Dascal, Nathan
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errSave
Genetic insights into childhood-onset schizophrenia: The yield of clinical exome sequencing
errSCHIZOPHRENIA RESEARCH
IF3.5
err2023-02-01
err7
PREAI
errAlkelai, Anna; Greenbaum, Lior; Shohat, Shahar; Povysil, Gundula; Malakar, Ayan; Ren, Zhong; Motelow, Joshua E.; Schechter, Tanya; Draiman, Benjamin; Chitrit-Raveh, Eti; Hughes, Daniel; Jobanputra, Vaidehi; Shifman, Sagiv; Goldstein, David B.; Kohn, Yoav
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errSave
Genome-wide Enrichment of TERT Rare Variants in Idiopathic Pulmonary Fibrosis Patients of Latino Ancestry
errAMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
IF19.4
err2022-10-01
err6
errOAAI
errZhang, David; Povysil, Gundula; Newton, Chad A.; Maher, Toby M.; Molyneaux, Philip L.; Noth, Imre; Martinez, Fernando J.; Raghu, Ganesh; Todd, Jamie L.; Palmer, Scott M.; Platt, Adam; Petrovski, Slave; Goldstein, David B.; Garcia, Christine Kim
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errSave
Utility of whole genome sequencing in assessing risk and clinically relevant outcomes for pulmonary fibrosis
errEUROPEAN RESPIRATORY JOURNAL
IF21
err2022-08-25
err16
errOAAI
errZhang, David; Newton, Chad A.; Wang, Binhan; Povysil, Gundula; Noth, Imre; Martinez, Fernando J.; Raghu, Ganesh; Goldstein, David; Garcia, Christine Kim
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errSave
Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
errKIDNEY INTERNATIONAL
IF12.6
err2022-06-01
err47
errOAAI
errKoettgen, Anna; Cornec-Le Gall, Emilie; Halbritter, Jan; Kiryluk, Krzysztof; Mallett, Andrew J.; Parekh, Rulan S.; Rasouly, Hila Milo; Sampson, Matthew G.; Tin, Adrienne; Antignac, Corinne; Ars, Elisabet; Bergmann, Carsten; Bleyer, Anthony J.; Bockenhauer, Detlef; Devuyst, Olivier; Florez, Jose C.; Fowler, Kevin J.; Franceschini, Nora; Fukagawa, Masafumi; Gale, Daniel P.; Gbadegesin, Rasheed A.; Goldstein, David B.; Grams, Morgan E.; Greka, Anna; Gross, Oliver; Guay-Woodford, Lisa M.; Harris, Peter C.; Hoefele, Julia; Hung, Adriana M.; Knoers, Nine V. A. M.; Kopp, Jeffrey B.; Kretzler, Matthias; Lanktree, Matthew B.; Lipska-Zietkiewicz, Beata S.; Nicholls, Kathleen; Nozu, Kandai; Ojo, Akinlolu; Parsa, Afshin; Pattaro, Cristian; Pei, York; Pollak, Martin R.; Rhee, Eugene P.; Sanna-Cherchi, Simone; Savige, Judy; Sayer, John A.; Scolari, Francesco; Sedor, John R.; Sim, Xueling; Somlo, Stefan; Susztak, Katalin; Tayo, Bamidele O.; Torra, Roser; van Eerde, Albertien M.; Weinstock, Andre; Winkler, Cheryl A.; Wuttke, Matthias; Zhang, Hong; King, Jennifer M.; Cheung, Michael; Jadoul, Michel; Winkelmayer, Wolfgang C.; Gharavi, Ali G.
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Ancestry adjustment improves genome-wide estimates of regional intolerance
errGENETICS
IF5.1
err2022-04-06
err2
errOAAI
errHayeck, Tristan J.; Stong, Nicholas; Baugh, Evan; Dhindsa, Ryan; Turner, Tychele N.; Malakar, Ayan; Mosbruger, Timothy L.; Shaw, Grace Tzun-Wen; Duan, Yuncheng; Ionita-Laza, Iuliana; Goldstein, David; Allen, Andrew S.
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Diagnostic sequencing to support genetically stratified medicine in a tertiary care setting
errGENETICS IN MEDICINE
IF6.2
err2022-04-01
err4
PREAI
errLippa, Natalie; Bier, Louise; Revah-Politi, Anya; May, Halie; Kushary, Sulagna; Vena, Natalie; Giordano, Jessica L.; Rasouly, Hila Milo; Cocchi, Enrico; Sands, Tristan T.; Wapner, Ronald J.; Anyane-Yeboa, Kwame; Gharavi, Ali G.; Goldstein, David B.
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Issues in interpreting results in research genomic testing for common disorders: an example within an OCD cohort
errGENETICS IN MEDICINE
IF6.2
err2022-03-01
err0
errOAAI
errRevah-Politi, Anya; (Tina) Kushary, Sulagna; Vena, Natalie; May, Halie; Lippa, Natalie; Bier, Louise; Goldman, Jill; Alkelai, Anna; Baugh, Evan; Zoghbi, Anthony; Kayser, Reilly; Goldstein, David; Simpson, H. Blair
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errSave
Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosis
errBONE
IF3.6
err2022-01-01
err13
errOAAI
errCohen, Adi; Hostyk, Joseph; Baugh, Evan H.; Buchovecky, Christie M.; Aggarwal, Vimla S.; Recker, Robert R.; Lappe, Joan M.; Dempster, David W.; Zhou, Hua; Kamanda-Kosseh, Mafo; Bucovsky, Mariana; Stubby, Julie; Goldstein, David B.; Shane, Elizabeth
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errSave
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca2+ regulation
errPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
IF9.1
err2021-12-20
err15
errOAAI
errHalvorsen, Matthew; Gould, Laura; Wang, Xiaohan; Grant, Gariel; Moya, Raquel; Rabin, Rachel; Ackerman, Michael J.; Tester, David J.; Lin, Peter T.; Pappas, John G.; Maurano, Matthew T.; Goldstein, David B.; Tsien, Richard W.; Devinsky, Orrin
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errSave
Focused goodness of fit tests for gene set analyses
errBRIEFINGS IN BIOINFORMATICS
IF7.7
err2021-11-27
err0
PREAI
errZhang, Mengqi; Gelfman, Sahar; Moreno, Cristiane Araujo Martins; McCarthy, Janice M.; Harms, Matthew B.; Goldstein, David B.; Allen, Andrew S.
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errSave
The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders
errMOLECULAR PSYCHIATRY
IF10.1
err2021-11-19
err12
PREAI
errAlkelai, Anna; Greenbaum, Lior; Docherty, Anna R.; Shabalin, Andrey A.; Povysil, Gundula; Malakar, Ayan; Hughes, Daniel; Delaney, Shannon L.; Peabody, Emma P.; McNamara, James; Gelfman, Sahar; Baugh, Evan H.; Zoghbi, Anthony W.; Harms, Matthew B.; Hwang, Hann-Shyan; Grossman-Jonish, Anat; Aggarwal, Vimla; Heinzen, Erin L.; Jobanputra, Vaidehi; Pulver, Ann E.; Lerer, Bernard; Goldstein, David B.
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Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders
errGENETICS IN MEDICINE
IF6.2
err2021-10-01
err8
errOAAI
errMay, Halie J.; Jeong, Jaehoon; Revah-Politi, Anya; Cohen, Julie S.; Chassevent, Anna; Baptista, Julia; Baugh, Evan H.; Bier, Louise; Bottani, Armand; Carminho A. Rodrigues, Maria Teresa; Conlon, Charles; Fluss, Joel; Guipponi, Michel; Kim, Chong Ae; Matsumoto, Naomichi; Person, Richard; Primiano, Michelle; Rankin, Julia; Shinawi, Marwan; Smith-Hicks, Constance; Telegrafi, Aida; Toy, Samantha; Uchiyama, Yuri; Aggarwal, Vimla; Goldstein, David B.; Roche, Katherine W.; Anyane-Yeboa, Kwame
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CLINICAL VALUE OF DIAGNOSTIC WHOLE GENOME/EXOME SEQUENCING IN FAMILIAL AUTISM SPECTRUM DISORDER
errEUROPEAN NEUROPSYCHOPHARMACOLOGY
IF6.7
err2021-10-01
err0
PREAI
errAlkelai, Anna; Greenbaum, Lior; Povysil, Gundula; Malakar, Ayan; Pras, Elon; Goldstein, David
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Research Directions

No research directions
Co-authors
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H-index: 199 · Papers: 1.6K
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