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T

Tamar Harel

Hadassah Medical Center

33H-index
160Paper Count
5.2KCitation Count
Published Papers 64
Publication Date
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CRISPR knockout screens reveal genes and pathways essential for neuronal differentiation and implicate PEDS1 in neurodevelopment
errNature Neuroscience
IF20
err2026-01-05
err0
PREAI
errAlana Amelan; Stephan C. Collins; Nadirah S. Damseh; Nanako Hamada; Ahd Salim; Elad Dvir; Galya Monderer-Rothkoff; Tamar Harel; Koh-ichi Nagata; Binnaz Yalcin; Sagiv Shifman
errShare
errSave
Inherent variability limits clinical utility of reproducible Parkinson’s transcriptomics signatures
errnpj Parkinson's Disease
IF8.2
err2025-12-19
err0
errOAAI
errRoy Dayan; Serafima Dubnov; Hagit Turm; Michelle Grunin; Shahar Shohat; Salim T. Khoury; Ami Citri; Tamar Harel; David Arkadir
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errSave
Reconsidering a silent variant: SGCA’s role in atypical cardiomyopathy
errEuropean Journal of Human Genetics
IF4.6
err2025-12-04
err0
errOAAI
errSmadar Horowitz-Cederboim; Ronit Hoffman-Lipschuetz; Ronen Durst; Shoshi Shpitzen; Ayelet Shauer; Donna R. Zwas; Chaggai Rosenbluh; Israel Antman; Avital Eilat; Tamar Harel; Orr Tomer; Vardiella Meiner
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Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies
errNature Communications
IF15.7
err2025-11-26
err0
errOAAI
errSébastien Küry; Janelle E. Stanton; Geeske M. van Woerden; Amélie Bosc-Rosati; Tzung-Chien Hsieh; Lise Bray; Marielle Oloudé; Cory Rosenfelt; Marie Pier Scott-Boyer; Victoria Most; Tianyun Wang; Jonas J. Papendorf; Charlotte de Konink; Wallid Deb; Virginie Vignard; Maja Studencka-Turski; Thomas Besnard; Anna M. Hajdukowicz; Franziska G. Thiel; Sophie Wolfgramm; Laëtitia Florenceau; Silvestre Cuinat; Sylvain Marsac; Yann Verrès; Audrey Dangoumau; Léa Poirier; Ingrid M. Wentzensen; Annabelle Tuttle; Cara Forster; Johanna Striesow; Richard Golnik; Damara Ortiz; Laura Jenkins; Jill A. Rosenfeld; Alban Ziegler; Clara Houdayer; Dominique Bonneau; Erin Torti; Amber Begtrup; Kristin G. Monaghan; Sureni V. Mullegama; Catharina M. L. Nienke Volker-Touw; Koen L. I. van Gassen; Renske Oegema; Mirjam S. de Pagter; Katharina Steindl; Anita Rauch; Ivan Ivanovski; Kimberly McDonald; Emily Boothe; Andrew Dauber; Janice Baker; Noelle Andrea V. Fabie; Raphael A. Bernier; Tychele N. Turner; Siddharth Srivastava; Kira A. Dies; Lindsay C. Swanson; Carrie Costin; Alali Abdulrazak; Rebekah K. Jobling; John Pappas; Rachel Rabin; Dmitriy Niyazov; Anne Chun-Hui Tsai; Karen Kovak; David B. Beck; May Christine V. Malicdan; David R. Adams; Lynne Wolfe; Rebecca D. Ganetzky; Colleen C. Muraresku; Davit Babikyan; Zdeněk Sedláček; Miroslava Hančárová; Andrew T. Timberlake; Hind Al Saif; Berkley Nestler; Kayla King; MJ Hajianpour; Gregory Costain; D’Arcy Prendergast; Chumei Li; David Geneviève; Antonio Vitobello; Arthur Sorlin; Christophe Philippe; Tamar Harel; Ori Toker; Ataf Sabir; Derek Lim; Mark J. Hamilton; Lisa J. Bryson; Elaine Cleary; Sacha Weber; Trevor L. Hoffman; Anna M. Cueto-González; Eduardo F. Tizzano; David Gómez-Andrés; Marta Codina-Solà; Athina Ververi; Efterpi Pavlidou; Alexandros Lambropoulos; Kyriakos Garganis; Marlène Rio; Jonathan Levy; Sarah J. Langas; Anne M. McRae; Mathieu K. Lessard; Maria Daniela D’Agostino; Isabelle De Bie; Meret Wegler; Rami Abou Jamra; Susanne B. Kamphausen; Viktoria Bothe; Lorraine Potocki; Eric Olinger; Yves Sznajer; Elsa Wiame; Michelle L. Thompson; Molly C. Schroeder; Catherine Gooch; Raphael A. Smith; Arti Pandya; Larissa M. Busch; Uwe Völker; Elke Hammer; Kristian Wende; Benjamin Cogné; Bertrand Isidor; Jens Meiler; Clémentine Ripoll; Stéphanie Bigou; Frédéric Laumonnier; Peter W. Hildebrand; Evan E. Eichler; Kirsty McWalter; Peter M. Krawitz; Florence Roux-Dalvai; Ype Elgersma; Julien Marcoux; Marie-Pierre Bousquet; Arnaud Droit; Jeremie Poschmann; Andreas M. Grabrucker; Francois V. Bolduc; Stéphane Bézieau; Frédéric Ebstein; Elke Krüger
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errSave
High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics
errClinical Genetics
IF2.3
err2025-09-27
err0
errOAAI
errRivka Birnbaum; Maya Slovik; Shamir Zenvirt; Ilana Livyatan; Israel Altman; Shiri Gershon; Jonathan Rips; Hagit Daum; Chaggai Rosenbluh; Orly Elpeleg; Vardiella Meiner; Ayala Frumkin; Hagar Mor-Shaked; Tamar Harel
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errSave
A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss-of-Function of DMRT2
errAMERICAN JOURNAL OF MEDICAL GENETICS PART A
IF1.7
err2025-09-01
err0
errOAAI
errRips, Jonathan; Mor-Shaked, Hagar; Shamriz, Oded; Somech, Raz; Abu Omar, Rawan; Eventov-Friedman, Smadar; Ofek-Shlomai, Noa; Zaguer, Dvorah; Harel, Tamar
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A founder variant in TBCB is associated with global developmental delay, autism spectrum and spastic paraparesis
errGenetics in Medicine
IF6.2
err2025-08-23
err0
PREAI
errSharon Bratman Morag; Chen Itzkovich; Alina Kurolap; Mordechai Shohat; Alexandra Durr; Jean-Madeleine de Sainte Agathe; Jeremy Bertrand; Arie Koifman; Anna Alkelai; Alan R. Shuldiner; Adi Mory; Tamar Harel; Hagar Mor-Shaked; Adel Shalata; Tamar Paperna; Hagit Baris Feldman; Reli Rachel Kakun; Daniel Kornitzer; Adi Salzberg; Karin Weiss
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errSave
Transcriptome analysis of atad3-null zebrafish embryos elucidates possible disease mechanisms
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2025-04-15
err0
errOAAI
errEzer, Shlomit; Ronin, Nathan; Yanovsky-Dagan, Shira; Rotem-Bamberger, Shahar; Halstuk, Orli; Wexler, Yair; Ben-Moshe, Zohar; Plaschkes, Inbar; Benyamini, Hadar; Saada, Ann; Inbal, Adi; Harel, Tamar
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Talin1 dysfunction is genetically linked to systemic capillary leak syndrome
errJCI INSIGHT
IF6.1
err2024-12-20
err0
errOAAI
errElefant, Naama; Rouni, Georgia; Arapatzi, Christina; Oz-Levi, Danit; Sion-Sarid, Racheli; Edwards, William J. S.; Ball, Neil J.; Yanovsky-Dagan, Shira; Cowell, Alana R.; Meiner, Vardiella; Vainstein, Vladimir; Grammenoudi, Sofia; Lancet, Doron; Goult, Benjamin T.; Harel, Tamar; Kostourou, Vassiliki
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Novel lamp3 gene mutation associated with variable clinical presentation of interstitial lung disease
errEUROPEAN RESPIRATORY JOURNAL
IF21
err2024-10-30
err0
PREAI
errHadhud, Mohamad; Rips, Jonathan; Harel, Tamar; Breuer, Oded
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Low prevalence of SCA27B in adult-onset cerebellar ataxia cohort of Jewish ancestry
errPARKINSONISM & RELATED DISORDERS
IF3.4
err2024-09-01
err0
PREAI
errHalstuk, Orli; Dayan, Roy; Silverstein, Shira; Fellig, Yakov; Saada, Ann; Harel, Tamar; Arkadir, David
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errSave
A deleterious variant of INTS1 leads to disrupted sleep-wake cycles
errDISEASE MODELS & MECHANISMS
IF3.3
err2024-08-27
err0
errOAAI
errConfino, Shir; Wexler, Yair; Medvetzky, Adar; Elazary, Yotam; Ben-Moshe, Zohar; Reiter, Joel; Dor, Talya; Edvardson, Simon; Prag, Gali; Harel, Tamar; Gothilf, Yoav
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De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features
errBRAIN
IF11.7
err2024-05-16
err1
errOAAI
errHarel, Tamar; Spicher, Camille; Scheer, Elisabeth; Buchan, Jillian G.; Cech, Jennifer; Folland, Chiara; Frey, Tanja; Holtz, Alexander M.; Innes, A. Micheil; Keren, Boris; Macken, William L.; Marcelis, Carlo; Otten, Catherine E.; Paolucci, Sarah A.; Petit, Florence; Pfundt, Rolph; Pitceathly, Robert D. S.; Rauch, Anita; Ravenscroft, Gianina; Sanchev, Rani; Steindl, Katharina; Tammer, Femke; Tyndall, Amanda; Devys, Didier; Vincent, Stephane D.; Elpeleg, Orly; Tora, Laszlo
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errSave
A neurodevelopmental disorder associated with a loss-of-function missense mutation in RAB35
errJOURNAL OF BIOLOGICAL CHEMISTRY
IF3.9
err2024-04-01
err0
errOAAI
errAguila, Adriana; Salah, Somaya; Kulasekaran, Gopinath; Shweiki, Moatasem; Shaul-Lotan, Nava; Mor-Shaked, Hagar; Daana, Muhannad; Harel, Tamar; Mcpherson, Peter S.
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Unbiased phenotype and genotype matching maximizes gene discovery and diagnostic yield
errGENETICS IN MEDICINE
IF6.2
err2024-04-01
err2
PREAI
errRips, Jonathan; Halstuk, Orli; Fuchs, Adina; Lang, Ziv; Sido, Tal; Gershon-Naamat, Shiri; Abu-Libdeh, Bassam; Edvardson, Simon; Salah, Somaya; Breuer, Oded; Hadhud, Mohamad; Eden, Sharon; Simon, Itamar; Slae, Mordechai; Damseh, Nadirah S.; Abu-Libdeh, Abdulsalam; Eskin-Schwartz, Marina; Birk, Ohad S.; Varga, Julia; Schueler-Furman, Ora; Rosenbluh, Chaggai; Elpeleg, Orly; Yanovsky-Dagan, Shira; Mor-Shaked, Hagar; Harel, Tamar
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USP27X variants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms
errLIFE SCIENCE ALLIANCE
IF2.9
err2024-01-05
err5
errOAAI
errKoch, Intisar; Slovik, Maya; Zhang, Yuling; Liu, Bingyu; Rennie, Martin; Konz, Emily; Cogne, Benjamin; Daana, Muhannad; Davids, Laura; Diets, Illja J.; Gold, Nina B.; Holtz, Alexander M.; Isidor, Bertrand; Mor-Shaked, Hagar; Fresneda, Juanita Neira; Niederhoffer, Karen Y.; Nizon, Mathilde; Pfundt, Rolph; Simon, Meh; Stegmann, Apa; Sacoto, Maria J. Guillen; Wevers, Marijke; Barakat, Tahsin Stefan; Yanovsky-Dagan, Shira; Atanassov, Boyko S.; Toth, Rachel; Gao, Chengjiang; Bustos, Francisco; Harel, Tamar
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Complex rearrangement in TBC1D4 in an individual with diabetes due to severe insulin resistance syndrome
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2023-12-12
err4
PREAI
errCahn, Avivit; Mor-Shaked, Hagar; Rosenberg-Fogler, Hallel; Pollack, Rena; Tolhuis, Bas; Sharma, Gaurav; Schultz, Eric; Yanovsky-Dagan, Shira; Harel, Tamar
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errSave
Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2023-12-01
err6
errOAAI
errEngal, Eden; Oja, Kaisa Teele; Maroofian, Reza; Geminder, Ophir; Le, Thuy-Linh; Marzin, Pauline; Guimier, Anne; Mor, Evyatar; Zvi, Naama; Elefant, Naama; Zaki, Maha S.; Gleeson, Joseph G.; Muru, Kai; Pajusalu, Sander; Wojcik, Monica H.; Pachat, Divya; Elmaksoud, Marwa Abd; Jeong, Won Chan; Lee, Hane; Bauer, Peter; Zifarelli, Giovanni; Houlden, Henry; Daana, Muhannad; Elpeleg, Orly; Amiel, Jeanne; Lyonnet, Stanislas; Gordon, Christopher T.; Harel, Tamar; Ounap, Katrin; Salton, Maayan; Mor-Shaked, Hagar
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Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2023-10-13
err1
PREAI
errBirnbaum, Rivka; Ezer, Shlomit; Lotan, Nava Shaul; Eilat, Avital; Sternlicht, Keren; Benyamini, Lilach; Reish, Orit; Falik-Zaccai, Tzipora; Ben-Gad, Gali; Rod, Raya; Segel, Reeval; Kim, Katherine; Burton, Barabra; Keegan, Catherine E.; Wagner, Mallory; Henderson, Lindsay B.; Mor, Nofar; Barel, Ortal; Hirsch, Yoel; Meiner, Vardiella; Elpeleg, Orly; Harel, Tamar; Mor-Shakad, Hagar
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Discovery of a new hereditary RECQ helicase disorder RECON syndrome positions the replication stress response and genome homeostasis as centrally important processes in aging and age-related disease
errAGEING RESEARCH REVIEWS
IF12.4
err2023-04-01
err2
errOAAI
errDatta, Arindam; Sommers, Joshua A.; Jhujh, Satpal S.; Harel, Tamar; Stewart, Grant S.; Brosh, Robert M.
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Research Directions

No research directions
Co-authors
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