Rivka Carmi (Hebrew: רבקה כרמי; born 1948) is an Israeli pediatrician and geneticist. She served as President of Ben-Gurion University of the Negev (BGU) from May 2006 until December 2018. Carmi is the first woman to be appointed president of an Israeli university.[1]
She was an officer in the Israeli Defence Forces (Captain), and served as the commander of academics officers' training school. During the Yom Kippur War, she helped establish the missing in action (MIA) accounting unit in the IDF.
Carmi is a member of the Advisory Board of the Genesis Prize Foundation.[34] She is a founding member of the UK-Israel Science Council and served as its co-chair alongside Professor Raymond Dwek in the years 2010–2017.[35] On April 4, 2013, the Minister of Justice, MP Tzipi Livni, appointed Carmi to be part of the Rivlin Committee. The committee examined the compensation agreement for workers of the nuclear research facility in Dimona that were exposed to ionizing radiation and diagnosed with cancer.
In May 2014 Carmi was appointed to the Locker Committee which examined Israel's national defense budget. In 2011 she was appointed chairperson of the Promotion and Representation of Women in Higher Education Institutions Committee (the Carmi Team).[36] In 2015 she headed the task force of the Israeli Medical Association established to study the status of women in medicine.
Between the years 2021 and 2023 she was the chairwoman of TELEM (the Council for National Research Infrastructures Committee for Bio-convergence).[37]
Currently (2025), Prof. Carmi serves as the Founding President of the Israel Academy of Science in Medicine by the Israeli Medical Association (founded in 2019),[38] Chairwoman of the TELEM Scientific Advisory Committee for Bio-convergence,[37] Chairwoman of ScienceAbroad,[39] chairwoman of the CHE Advisory Committee on Medical Education,[1] Research fellow at the Shmuel Neeman Institute,[40] board member - 8400,[41] Levinski-Wingate Academic Center,[42] Desert stars and additional startups boards.[43]
Controversy
In November 2017, the search committee for president recommended extending Carmi's tenure as president by two additional years, through May 2020. In response, the academic senate held an extraordinary meeting, in which it declared that the search committee failed and called for the resignation of the chair of the executive committee, Asher Heled.[44] The executive committee decided to approve the extension despite the objections of the academic staff, which resulted in further protest.[45] The State Comptroller of Israel launched an investigation into the selection process.[46] In response, Carmi stated: "What I have in mind is the good of the university, so once a person is elected to head it, I will be the first to congratulate, to vacate my place and to pave the way for anyone found to be suitable – even if it is earlier than the two years that I was asked to fill.[47]
In February 2018, the executive committee announced that a new president would be elected by the end of year.[48]
2003 – Achievement in Medicine Award by the Municipality of Beer–Sheva
2002 – Award for Peace from the Canada International Scientific Exchange Program (CISEPO), to which she served as representative of the Israeli Medical Deans
2001 – Lifetime Achievement Award by the Yated organization for children with Downs Syndrome
^Bet-Or H, Weizman D, Elbedour K, Shoham-Vardi I, Carmi R (2000). "Community based program to prevent hereditary deafness among the negev bedouins in israel". J Med Genet. A15 (37).
^Raz, Aviad E.; Atar, Marcela; Rodnay, Maya; Shoham-Vardi, Ilana; Carmi, Rivka (2003). "Between Acculturation and Ambivalence: Knowledge of Genetics and Attitudes towards Genetic Testing in a Consanguineous Bedouin Community". Public Health Genomics. 6 (2): 88–95. doi:10.1159/000073004. PMID14560069. S2CID10952354.
^Birnbaum, Ramon Y.; Landau, Daniella; Elbedour, Khalil; Ofir, Rivka; Birk, Ohad S.; Carmi, Rivka (15 April 2008). "Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients". American Journal of Medical Genetics Part A. 146A (8): 1063–1066. doi:10.1002/ajmg.a.31903. ISSN1552-4833. PMID18348258. S2CID205308681.
^Mykytyn, Kirk; Nishimura, Darryl Y.; Searby, Charles C.; Shastri, Mythreyi; Yen, Hsan-jan; Beck, John S.; Braun, Terry; Streb, Luan M.; Cornier, Alberto S. (1 August 2002). "Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome". Nature Genetics. 31 (4): 435–438. doi:10.1038/ng935. ISSN1061-4036. PMID12118255. S2CID29915446.
^Walder, Roxanne Y.; Landau, Daniel; Meyer, Peter; Shalev, Hanna; Tsolia, Maria; Borochowitz, Zvi; Boettger, Melanie Barbara; Beck, Gretel E.; Englehardt, Richard K. (1 June 2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nature Genetics. 31 (2): 171–174. doi:10.1038/ng901. ISSN1061-4036. PMID12032570. S2CID33192419.
^Haider, Neena B.; Jacobson, Samuel G.; Cideciyan, Artur V.; Swiderski, Ruth; Streb, Luan M.; Searby, Charles; Beck, Gretel; Hockey, Robin; Hanna, David B. (1 February 2000). "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate". Nature Genetics. 24 (2): 127–131. doi:10.1038/72777. ISSN1061-4036. PMID10655056. S2CID19508439.
^Buskila, Dan; Neumann, Lily; Hazanov, Ilia; Carmi, Rivka (1 December 1996). "Familial aggregation in the fihromyalgia syndrome". Seminars in Arthritis and Rheumatism. 26 (3): 605–611. doi:10.1016/S0049-0172(96)80011-4. PMID8989805.
^Carmi, R.; Rokhlina, T.; Kwitek-Black, A. E.; Elbedour, K.; Nishimura, D.; Stone, E. M.; Sheffield, V. C. (1 January 1995). "Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15". Human Molecular Genetics. 4 (1): 9–13. doi:10.1093/hmg/4.1.9. ISSN0964-6906. PMID7711739.
^Sheffield, Val C.; Carml, Rivka; Kwltek-Black, Anne; Rokhlina, Tatiana; Nishlmura, Darryl; Duyk, Geoffrey M.; Elbedour, Khalil; Sunden, Sara L.; Stone, Edwin M. (1 August 1994). "Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping". Human Molecular Genetics. 3 (8): 1331–1335. doi:10.1093/hmg/3.8.1331. ISSN0964-6906. PMID7987310.
^Carmi, R.; Gohar, J.; Meizner, I.; Katz, M. (1 June 1994). "Spontaneous abortion–high risk factor for neural tube defects in subsequent pregnancy". American Journal of Medical Genetics. 51 (2): 93–97. doi:10.1002/ajmg.1320510203. ISSN1096-8628. PMID8092200.
^Parvari, R.; Weinstein, Y.; Ehrlich, S.; Steinitz, M.; Carmi, R. (15 February 1994). "Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25–26". American Journal of Medical Genetics. 49 (4): 431–434. doi:10.1002/ajmg.1320490416. ISSN1096-8628. PMID7909197.
^Kwitek-Black, Anne E.; Carmi, Rivka; Duyk, Geoffrey M.; Buetow, Kenneth H.; Elbedour, Khalil; Parvari, Ruti; Yandava, Chandra Naidu; Stone, Edwin M.; Sheffield, Val C. (1 December 1993). "Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity". Nature Genetics. 5 (4): 392–396. doi:10.1038/ng1293-392. PMID8298649. S2CID30898539.
^Carmi, Rivka; Boughman, Joann A. (1 January 1992). "Pentalogy of Cantrell and associated midline anomalies: A possible ventral midline developmental field". American Journal of Medical Genetics. 42 (1): 90–95. doi:10.1002/ajmg.1320420118. ISSN1096-8628. PMID1308371.
^Carmi, R.; Meizner, I.; Katz, M. (1 July 1990). "Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X-linked midline gene?". American Journal of Medical Genetics. 36 (3): 313–315. doi:10.1002/ajmg.1320360314. ISSN1096-8628. PMID2363430.
^Carmi, R.; Sofer, S.; Karplus, M.; Ben-Yakar, Y.; Mahler, D.; Zirkin, H.; Bar-Ziv, J.; Opitz, John M. (1 March 1982). "Aplasia cutis congenita in two sibs discordant for pylori atresia". American Journal of Medical Genetics. 11 (3): 319–328. doi:10.1002/ajmg.1320110308. ISSN1096-8628. PMID6177243.
^Carmi, R.; Barbash, A.; Mares, A. J. (1 May 1990). "The thoracoabdominal syndrome (TAS): A new X-linked dominant disorder". American Journal of Medical Genetics. 36 (1): 109–114. doi:10.1002/ajmg.1320360122. ISSN1096-8628. PMID2139758.