Research output per year
Research output per year
- 1 - 50 out of 173 results
Search results
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2024
A novel RYR1 pathogenic variant − Common among Libyan Jews and associated with a broad phenotypic spectrum
Regev, M., Dori, A., Altarescu, G., Barel, O., Basel-Salmon, L., Greenbaum, L., Fellner, A., Pras, E., Shamash, J., Meiner, V., Bazak, L. & Goldberg, Y., 15 Nov 2024, In: Gene. 927, 148725.Research output: Contribution to journal › Article › peer-review
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Expanded targeted preconception screening panel in Israel: findings and insights
Reches, A., Ofen Glassner, V., Goldstein, N., Yeshaya, J., Delmar, G., Portugali, E., Hallas, T., Weinstein, A., Kurolap, A., Berkenstadt, M., Mantsour, T., Abu-Gutstein, L., Ries-Levavi, L., Reznik-Wolf, H., Behar, D. M., Yaron, Y., Pras, E. & Baris Feldman, H., 19 Jul 2024, In: Journal of Medical Genetics. 61, 8, p. 783-787 5 p.Research output: Contribution to journal › Article › peer-review
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The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting
Lempel, N., Shelly, S., Chorin, O., Rock, R., Eliyahu, A., Finezilber, Y., Poran, H., Feinstein-Goren, N., Segev, M., Reznik-Wolf, H., Barel, O., Orion, D., Anis, S., Regev, M., Yonath, H., Dominissini, D., Blatt, I., Hassin-Baer, S., Dori, A. & Pras, E. & 1 others, , 15 Aug 2024, In: Journal of the Neurological Sciences. 463, 123074.Research output: Contribution to journal › Article › peer-review
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2023
Adult-onset Alexander disease among patients of Jewish Syrian descent
Anis, S., Fay-Karmon, T., Lassman, S., Shbat, F., Lesman-Segev, O., Mor, N., Barel, O., Dominissini, D., Chorin, O., Pras, E., Greenbaum, L. & Hassin-Baer, S., Oct 2023, In: Neurogenetics. 24, 4, p. 303-310 8 p.Research output: Contribution to journal › Article › peer-review
2 Scopus citations -
Bath psoralen plus ultraviolet-A photochemotherapy for chronic graft-versus-host disease: a retrospective cohort study
Kassem, R., Barzilai, A., Pras, E., Sizopoulou, C. & Pavlotsky, F., Oct 2023, In: International Journal of Dermatology. 62, 10, p. 1261-1265 5 p.Research output: Contribution to journal › Article › peer-review
Open Access -
CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a−) variant
Kurolap, A., Hagin, D., Freund, T., Fishman, S., Zunz Henig, N., Brazowski, E., Yeshaya, J., Naiman, T., Pras, E., Ablin, J. N. & Baris Feldman, H., May 2023, In: Human Genetics. 142, 5, p. 683-690 8 p.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features
Dori, A., Arad, M., Wasserstrum, Y., Pollak, A., Nikitin, V., Ben-David, M., Shamash, J., Nahum, A. H., Shavit-Stein, E., Domachevsky, L., Kuperstein, R., Dominissini, D., Shelestovich, N., Sadeh, M., Pras, E. & Greenbaum, L., Apr 2023, In: Annals of Clinical and Translational Neurology. 10, 4, p. 553-567 15 p.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
2022
Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay
Eliyahu, A., Barel, O., Greenbaum, L., Zaks Hoffer, G., Goldberg, Y., Raas-Rothschild, A., Singer, A., Bar-Joseph, I., Kunik, V., Javasky, E., Staretz-Chacham, O., Pode-Shakked, N., Bazak, L., Ruhrman-Shahar, N., Pras, E., Frydman, M., Shohat, M. & Pode-Shakked, B., 30 Mar 2022, In: Frontiers in Pediatrics. 10, 844845.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
2021
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies
Pode-Shakked, B., Barel, O., Singer, A., Regev, M., Poran, H., Eliyahu, A., Finezilber, Y., Segev, M., Berkenstadt, M., Yonath, H., Reznik-Wolf, H., Gazit, Y., Chorin, O., Heimer, G., Gabis, L. V., Tzadok, M., Nissenkorn, A., Bar-Yosef, O., Zohar-Dayan, E. & Ben-Zeev, B. & 16 others, , Dec 2021, In: Scientific Reports. 11, 1, 19099.Research output: Contribution to journal › Article › peer-review
Open Access13 Scopus citations -
Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population
Greenbaum, L., Ben-David, M., Nikitin, V., Gera, O., Barel, O., Hersalis-Eldar, A., Shamash, J., Shimshoviz, N., Reznik-Wolf, H., Shohat, M., Dominissini, D., Pras, E. & Dori, A., Jun 2021, In: Annals of Clinical and Translational Neurology. 8, 6, p. 1260-1268 9 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutation
Domniz, N., Levavi, L. R., Berkenstadt, M., Pras, E., Cohen, Y., Raanani, H., Goldstein, D. B., Yaron, Y., Elizur, S. & Ben-Shachar, S., Jun 2021, In: Genetics in Medicine. 23, 6, p. 1023-1027 5 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin
Wilf-Yarkoni, A., Shor, O., Fellner, A., Hellmann, M. A., Pras, E., Yonath, H., Shkedi-Rafid, S., Basel-Salmon, L., Bazak, L., Eliahou, R., Greenbaum, L., Stiebel-Kalish, H., Benninger, F. & Goldberg, Y., 19 Apr 2021, In: Neurology: Genetics. 7, 2, p. e578Research output: Contribution to journal › Article › peer-review
Open Access10 Scopus citations -
The role of orotic acid measurement in routine newborn screening for urea cycle disorders
Staretz-Chacham, O., Daas, S., Ulanovsky, I., Blau, A., Rostami, N., Saraf-Levy, T., Abu Salah, N., Anikster, Y., Banne, E., Dar, D., Dumin, E., Fattal-Valevski, A., Falik-Zaccai, T., Hershkovitz, E., Josefsberg, S., Khammash, H., Keidar, R., Korman, S. H., Landau, Y. & Lerman-Sagie, T. & 18 others, , May 2021, In: Journal of Inherited Metabolic Disease. 44, 3, p. 606-617 12 p.Research output: Contribution to journal › Article › peer-review
7 Scopus citations -
קדחת ים תיכונית משפחתית והשירות בצה"ל: [מאמרים]
Translated title of the contribution :Familial Mediterranean Fever and Service in the Israel Defense Forces Research output: Contribution to journal › Article › peer-review
Open Access -
2020
Chromosomal microarray evaluation of fetal ventriculomegaly
Toren, A., Alpern, S., Berkenstadt, M., Bar-Yosef, O., Pras, E. & Katorza, E., Oct 2020, In: Israel Medical Association Journal. 22, 10, p. 573-578 6 p.Research output: Contribution to journal › Article › peer-review
7 Scopus citations -
Clues and challenges in the diagnosis of intermittent maple syrup urine disease
Pode-Shakked, N., Korman, S. H., Pode-Shakked, B., Landau, Y., Kneller, K., Abraham, S., Shaag, A., Ulanovsky, I., Daas, S., Saraf-Levy, T., Reznik-Wolf, H., Vivante, A., Pras, E., Almashanu, S. & Anikster, Y., Jun 2020, In: European Journal of Medical Genetics. 63, 6, 103901.Research output: Contribution to journal › Article › peer-review
20 Scopus citations -
Familial Mediterranean fever: Penetrance of the p.[Met694Val];[Glu148Gln] and p.[Met694Val];[=] genotypes
Eyal, O., Shinar, Y., Pras, M. & Pras, E., 1 Nov 2020, In: Human Mutation. 41, 11, p. 1866-1870 5 p.Research output: Contribution to journal › Article › peer-review
Open Access13 Scopus citations -
Familial Mediterranean fever is associated with increased risk for ischaemic heart disease and mortality–Perspective derived from a large database
Gendelman, O., Shapira, R., Tiosano, S., Pras, E., Comaneshter, D., Cohen, A. & Amital, H., 1 May 2020, In: International Journal of Clinical Practice. 74, 5, e13473.Research output: Contribution to journal › Article › peer-review
Open Access16 Scopus citations -
Identification of a homozygous VRK1 mutation in two patients with adult-onset distal hereditary motor neuropathy
Greenbaum, L., Barel, O., Nikitin, V., Hersalis-Eldar, A., Kol, N., Reznik-Wolf, H., Dominissini, D., Pras, E. & Dori, A., 1 Mar 2020, In: Muscle and Nerve. 61, 3, p. 395-400 6 p.Research output: Contribution to journal › Article › peer-review
9 Scopus citations -
Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi Jews
Oz, S., Yonath, H., Visochyk, L., Ofek, E., Landa, N., Reznik-Wolf, H., Ortiz-Genga, M., Monserrat, L., Ben-Gal, T., Goitein, O., Beinart, R., Glikson, M., Freimark, D., Pras, E., Arad, M. & Nof, E., 15 Oct 2020, In: International Journal of Cardiology. 317, p. 133-138 6 p.Research output: Contribution to journal › Article › peer-review
Open Access12 Scopus citations -
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1
Brownstein, Z., Gulsuner, S., Walsh, T., Martins, F. T. A., Taiber, S., Isakov, O., Lee, M. K., Bordeynik-Cohen, M., Birkan, M., Chang, W., Casadei, S., Danial-Farran, N., Abu-Rayyan, A., Carlson, R., Kamal, L., Arnthórsson, A., Sokolov, M., Gilony, D., Lipschitz, N. & Frydman, M. & 30 others, , 1 Oct 2020, In: Clinical Genetics. 98, 4, p. 353-364 12 p.Research output: Contribution to journal › Article › peer-review
Open Access17 Scopus citations -
2019
BRPF1-associated intellectual disability, ptosis, and facial dysmorphism in a multiplex family
Pode-Shakked, N., Barel, O., Pode-Shakked, B., Eliyahu, A., Singer, A., Nayshool, O., Kol, N., Raas-Rothschild, A., Pras, E. & Shohat, M., Jun 2019, In: Molecular genetics & genomic medicine. 7, 6, e665.Research output: Contribution to journal › Article › peer-review
Open Access22 Scopus citations -
Noncoding deletions reveal a gene that is critical for intestinal function
Oz-Levi, D., Olender, T., Bar-Joseph, I., Zhu, Y., Marek-Yagel, D., Barozzi, I., Osterwalder, M., Alkelai, A., Ruzzo, E. K., Han, Y., Vos, E. S. M., Reznik-Wolf, H., Hartman, C., Shamir, R., Weiss, B., Shapiro, R., Pode-Shakked, B., Tatarskyy, P., Milgrom, R. & Schvimer, M. & 23 others, , 4 Jul 2019, In: Nature. 571, 7763, p. 107-111 5 p.Research output: Contribution to journal › Article › peer-review
Open Access22 Scopus citations -
Prenatal diagnosis for de novo mutations: Experience from a tertiary center over a 10-year period
Eyal, O., Berkenstadt, M., Reznik-Wolf, H., Poran, H., Ziv-Baran, T., Greenbaum, L., Yonath, H. & Pras, E., Apr 2019, In: Molecular genetics & genomic medicine. 7, 4, e00573.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
2018
Absence of AGG Interruptions Is a Risk Factor for Full Mutation Expansion Among Israeli FMR1 Premutation Carriers
Domniz, N., Ries-Levavi, L., Cohen, Y., Marom-Haham, L., Berkenstadt, M., Pras, E., Glicksman, A., Tortora, N., Latham, G. J., Hadd, A. G., Nolin, S. L. & Elizur, S. E., 13 Dec 2018, In: Frontiers in Genetics. 9, 606.Research output: Contribution to journal › Article › peer-review
Open Access12 Scopus citations -
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi Jews
De Boer, M., Gavrieli, R., Van Leeuwen, K., Wolf, H. R., Dushnitzki, M., Bar-Yosef, Y., Bar-Ziv, A., Behar, D., Lipitz, S., Miller, T. E., Tool, A. T. J., Kuijpers, T. W., Van Den Berg, T. K., Wolach, B., Roos, D. & Pras, E., Mar 2018, In: Journal of Medical Genetics. 55, 3, p. 166-172 7 p.Research output: Contribution to journal › Article › peer-review
6 Scopus citations -
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin
Heimer, G., Eyal, E., Zhu, X., Ruzzo, E. K., Marek-Yagel, D., Sagiv, D., Anikster, Y., Reznik-Wolf, H., Pras, E., Oz Levi, D., Lancet, D., Ben-Zeev, B. & Nissenkorn, A., Jan 2018, In: European Journal of Paediatric Neurology. 22, 1, p. 93-101 9 p.Research output: Contribution to journal › Article › peer-review
36 Scopus citations -
SMYD1 is the underlying gene for the AnWj-negative blood group phenotype
Yahalom, V., Pillar, N., Zhao, Y., Modan, S., Fang, M., Yosephi, L., Asher, O., Shinar, E., Celniker, G., Resnik-Wolf, H., Brantz, Y., Hauschner, H., Rosenberg, N., Cheng, L., Shomron, N. & Pras, E., Oct 2018, In: European Journal of Haematology. 101, 4, p. 496-501 6 p.Research output: Contribution to journal › Article › peer-review
7 Scopus citations -
2017
A high and equal prevalence of the Q703K variant in NLRP3 patients with autoinflammatory symptoms and ethnically matched controls
Lidar, M., Brantz, Y., Shinar, Y., Reznik-Wolf, H., Livneh, A., Zvi, I. B., Cohen, R., Berkun, Y., Hashkes, P. J., Peleg, H., Kessel, A., Slobodin, G., Rozenbaum, M., Goldzweig, O. & Pras, E., 2017, In: Clinical and Experimental Rheumatology. 35, p. S82-S85Research output: Contribution to journal › Article › peer-review
4 Scopus citations -
Anakinra for Colchicine-Resistant Familial Mediterranean Fever: A Randomized, Double-Blind, Placebo-Controlled Trial
Ben-Zvi, I., Kukuy, O., Giat, E., Pras, E., Feld, O., Kivity, S., Perski, O., Bornstein, G., Grossman, C., Harari, G., Lidar, M. & Livneh, A., 1 Apr 2017, In: Arthritis and Rheumatology. 69, 4, p. 854-862 9 p.Research output: Contribution to journal › Article › peer-review
Open Access134 Scopus citations -
Colorectal and endometrial cancer risk and age at diagnosis in BLMAsh mutation carriers
Schayek, H., Laitman, Y., Katz, L. H., Pras, E., Ries-Levavi, L., Barak, F. & Friedman, E., Jun 2017, In: Israel Medical Association Journal. 19, 6, p. 365-367 3 p.Research output: Contribution to journal › Article › peer-review
9 Scopus citations -
Novelties in the field of autoimmunity – 1st Saint Petersburg congress of autoimmunity, the bridge between east and west
Dahan, S., Segal, Y., Watad, A., Azrielant, S., Shemer, A., Maymon, D., Stroev, Y. I., Sobolevskaya, P. A., Korneva, E. A., Blank, M., Gilburd, B., Shovman, O., Amital, H., Ehrenfeld, M., Tanay, A., Kivity, S., Pras, E., Chapman, J., Damoiseaux, J. & Cervera, R. & 13 others, , Dec 2017, In: Autoimmunity Reviews. 16, 12, p. 1175-1184 10 p.Research output: Contribution to journal › Article › peer-review
Open Access15 Scopus citations -
2016
A role for TENM1 mutations in congenital general anosmia
Alkelai, A., Olender, T., Haffner-Krausz, R., Tsoory, M. M., Boyko, V., Tatarskyy, P., Gross-Isseroff, R., Milgrom, R., Shushan, S., Blau, I., Cohn, E., Beeri, R., Levy-Lahad, E., Pras, E. & Lancet, D., 1 Sep 2016, In: Clinical Genetics. 90, 3, p. 211-219 9 p.Research output: Contribution to journal › Article › peer-review
47 Scopus citations -
Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing
Gal, M., Khermesh, K., Barak, M., Lin, M., Lahat, H., Wolf, H. R., Lin, M., Pras, E. & Levanon, E. Y., 2016, In: BMC Medical Genomics. 9, 1, 24.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Fishing for genes in autoimmunity
Regev, M. & Pras, E., 1 Mar 2016, In: Israel Medical Association Journal. 18, 3-4, p. 209-211 3 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects
Simon, A. J., Lev, A., Zhang, Y., Weiss, B., Rylova, A., Eyal, E., Kol, N., Barel, O., Cesarkas, K., Soudack, M., Greenberg-Kushnir, N., Rhodes, M., Wiest, D. L., Schiby, G., Barshack, I., Katz, S., Pras, E., Poran, H., Reznik-Wolf, H. & Ribakovsky, E. & 13 others, , 25 Jul 2016, In: Journal of Experimental Medicine. 213, 8, p. 1429-1440 12 p.Research output: Contribution to journal › Article › peer-review
Open Access99 Scopus citations -
Patients’ Attitudes Towards Disclosure of Genetic Test Results to Family Members: The Impact of Patients’ Sociodemographic Background and Counseling Experience
Gilbar, R., Shalev, S., Spiegel, R., Pras, E., Berkenstadt, M., Sagi, M., Ben-Yehuda, A., Mor, P., Perry, S., Zaccai, T. F., Borochowitz, Z. & Barnoy, S., 1 Apr 2016, In: Journal of Genetic Counseling. 25, 2, p. 314-324 11 p.Research output: Contribution to journal › Article › peer-review
Open Access8 Scopus citations -
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability
Heimer, G., Oz-Levi, D., Eyal, E., Edvardson, S., Nissenkorn, A., Ruzzo, E. K., Szeinberg, A., Maayan, C., Mai-Zahav, M., Efrati, O., Pras, E., Reznik-Wolf, H., Lancet, D., Goldstein, D. B., Anikster, Y., Shalev, S. A., Elpeleg, O. & Ben Zeev, B., 1 Jan 2016, In: European Journal of Paediatric Neurology. 20, 1, p. 69-79 11 p.Research output: Contribution to journal › Article › peer-review
36 Scopus citations -
The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers
Laitman, Y., Boker-Keinan, L., Berkenstadt, M., Liphsitz, I., Weissglas-Volkov, D., Ries-Levavi, L., Sarouk, I., Pras, E. & Friedman, E., 1 Mar 2016, In: Cancer genetics. 209, 3, p. 70-74 5 p.Research output: Contribution to journal › Article › peer-review
28 Scopus citations -
Very Early In-Utero Diagnosis of Walker-Warburg Phenotype: The Cutting Edge of Technology
Achiron, R., Katorza, E., Reznik-Wolf, H., Pras, E., Kidron, D. & Berkenstadtt, M., 1 May 2016, In: Ultrasound International Open. 2, 2, p. E54-E57Research output: Contribution to journal › Article › peer-review
Open Access8 Scopus citations -
2015
A novel mutation in the C7orf11 gene causes nonphotosensitive trichothiodystrophy in a multiplex highly consanguineous kindred
Pode-Shakked, B., Marek-Yagel, D., Greenberger, S., Pode-Shakked, N., Pras, E., Barzilai, A., Yassin, S., Sidi, Y. & Anikster, Y., 2015, In: European Journal of Medical Genetics. 58, 12, p. 685-688 4 p.Research output: Contribution to journal › Article › peer-review
6 Scopus citations -
A Priori Attitudes Predict Amniocentesis Uptake in Women of Advanced Maternal Age: A Pilot Study
Grinshpun-Cohen, J., Miron-Shatz, T., Rhee-Morris, L., Briscoe, B., Pras, E. & Towner, D., 2 Sep 2015, In: Journal of Health Communication. 20, 9, p. 1107-1113 7 p.Research output: Contribution to journal › Article › peer-review
10 Scopus citations -
Exome sequencing as a differential diagnosis tool: Resolving mild trichohepatoenteric syndrome
Oz-Levi, D., Weiss, B., Lahad, A., Greenberger, S., Pode-Shakked, B., Somech, R., Olender, T., Tatarsky, P., Marek-Yagel, D., Pras, E., Anikster, Y. & Lancet, D., 1 Jun 2015, In: Clinical Genetics. 87, 6, p. 602-603 2 p.Research output: Contribution to journal › Letter › peer-review
14 Scopus citations -
Factors that affect the decision to undergo amniocentesis in women with normal Down syndrome screening results: It is all about the age
Grinshpun-Cohen, J., Miron-Shatz, T., Ries-Levavi, L. & Pras, E., 1 Dec 2015, In: Health Expectations. 18, 6, p. 2306-2317 12 p.Research output: Contribution to journal › Article › peer-review
Open Access14 Scopus citations -
Founder mutation for Huntington disease in Caucasus Jews
Melamed, O., Behar, D. M., Bram, C., Magal, N., Pras, E., Reznik-Wolf, H., Borochowitz, Z. U., Davidov, B., Mor-Cohen, R. & Baris, H. N., 1 Feb 2015, In: Clinical Genetics. 87, 2, p. 167-172 6 p.Research output: Contribution to journal › Article › peer-review
6 Scopus citations -
Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration
Pras, E., Kristal, D., Shoshany, N., Volodarsky, D., Vulih, I., Celniker, G., Isakov, O., Shomron, N. & Pras, E., 2015, In: Journal of Medical Genetics. 52, 7, p. 484-492 9 p.Research output: Contribution to journal › Article › peer-review
20 Scopus citations -
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum
Heimer, G., Marek-Yagel, D., Eyal, E., Barel, O., Oz Levi, D., Hoffmann, C., Ruzzo, E. K., Ganelin-Cohen, E., Lancet, D., Pras, E., Rechavi, G., Nissenkorn, A., Anikster, Y., Goldstein, D. B. & Ben Zeev, B., 1 Oct 2015, In: Clinical Genetics. 88, 4, p. 327-335 9 p.Research output: Contribution to journal › Article › peer-review
44 Scopus citations -
The limited effect of information on Israeli pregnant women at advanced maternal age who decide to undergo amniocentesis
Grinshpun-Cohen, J., Miron-Shatz, T., Berkenstet, M. & Pras, E., 17 Aug 2015, In: Israel Journal of Health Policy Research. 4, 1, 23.Research output: Contribution to journal › Article › peer-review
Open Access14 Scopus citations -
Whole-exome sequencing in undiagnosed genetic diseases: Interpreting 119 trios
Zhu, X., Petrovski, S., Xie, P., Ruzzo, E. K., Lu, Y. F., McSweeney, K. M., Ben-Zeev, B., Nissenkorn, A., Anikster, Y., Oz-Levi, D., Dhindsa, R. S., Hitomi, Y., Schoch, K., Spillmann, R. C., Heimer, G., Marek-Yagel, D., Tzadok, M., Han, Y., Worley, G. & Goldstein, J. & 7 others, , 1 Oct 2015, In: Genetics in Medicine. 17, 10, p. 774-781 8 p.Research output: Contribution to journal › Article › peer-review
Open Access263 Scopus citations -
2014
Collaboration in response to disaster - Typhoon Yolanda and an integrative model
Merin, O., Kreiss, Y., Lin, G., Pras, E. & Dagan, D., 2014, In: New England Journal of Medicine. 370, 13, p. 1183-1184 2 p.Research output: Contribution to journal › Article › peer-review
22 Scopus citations