CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice
Halperin, D., Stavsky, A., Kadir, R., Drabkin, M., Wormser, O., Yogev, Y., Dolgin, V., Proskorovski-Ohayon, R., Perez, Y., Nudelman, H., Stoler, O., Rotblat, B., Lifschytz, T., Lotan, A., Meiri, G., Gitler, D., Birk, O. S.
Published in Nature communications (26.10.2021)
Published in Nature communications (26.10.2021)
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Journal Article
Vaccination Against Autoimmune Mouse Diabetes with a T-Cell Epitope of the Human 65-kDa Heat Shock Protein
Elias, Dana, Reshef, Tamara, Birk, Ohad S., van der Zee, Ruurd, Walker, Michael D., Cohen, Irun R.
Published in Proceedings of the National Academy of Sciences - PNAS (15.04.1991)
Published in Proceedings of the National Academy of Sciences - PNAS (15.04.1991)
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Novel SBF1 splice‐site null mutation broadens the clinical spectrum of Charcot‐Marie‐Tooth type 4B3 disease
Flusser, H., Halperin, D., Kadir, R., Shorer, Z., Shelef, I., Birk, O.S.
Published in Clinical genetics (01.11.2018)
Published in Clinical genetics (01.11.2018)
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Journal Article
Hsp60 peptide therapy of NOD mouse diabetes induces a Th2 cytokine burst and downregulates autoimmunity to various beta-cell antigens
Elias, D., Meilin, A., Ablamunits, V., Birk, O. S., Carmi, P., Konen-Waisman, S., Cohen, I. R.
Published in Diabetes (New York, N.Y.) (01.05.1997)
Published in Diabetes (New York, N.Y.) (01.05.1997)
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Journal Article
Gene expression microarray profiles of cumulus cells in lean and overweight-obese polycystic ovary syndrome patients
Kenigsberg, Shlomit, Bentov, Yaakov, Chalifa-Caspi, Vered, Potashnik, Gad, Ofir, Rivka, Birk, Ohad S.
Published in Molecular human reproduction (01.02.2009)
Published in Molecular human reproduction (01.02.2009)
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A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindred
Landau, D, Cohen, D, Shalev, H, Pinsk, V, Yerushalmi, B, Zeigler, M, Birk, O.S
Published in Molecular genetics and metabolism (01.06.2004)
Published in Molecular genetics and metabolism (01.06.2004)
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A Role of Hsp60 in Autoimmune Diabetes: Analysis in a Transgenic Model
Birk, Ohad S., Douek, Daniel C., Elias, Dana, Takacs, Katalin, Dewchand, Hamlata, Gur, Sara L., Walker, Michael D., Van Der Zee, Ruurd, Cohen, Irun R., Altmann, Daniel M.
Published in Proceedings of the National Academy of Sciences - PNAS (06.02.1996)
Published in Proceedings of the National Academy of Sciences - PNAS (06.02.1996)
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The LIM homeobox gene Lhx9 is essential for mouse gonad formation
Westphal, Heiner, Birk, Ohad S, Casiano, Delane E, Wassif, Christopher A, Cogliati, Tiziana, Zhao, Liping, Zhao, Yangu, Grinberg, Alexander, Huang, SingPing, Kreidberg, Jordan A, Parker, Keith L, Porter, Forbes D
Published in Nature (London) (24.02.2000)
Published in Nature (London) (24.02.2000)
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CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and jewish kindreds
BAR-YOSEF, Udy, ABUELAISH, Izzeldin, HAREL, Tamar, HENDLER, Neta, OFIR, Rivka, BIRK, Ohad S
Published in Human genetics (01.09.2004)
Published in Human genetics (01.09.2004)
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Journal Article
The 60-kDa Heat Shock Protein Modulates Allograft Rejection
Birk, Ohad S., Gur, Sara L., Elias, Dana, Margalit, Raanan, Mor, Felix, Carmi, Pnina, Bockova, Jana, Altmann, Daniel M., Cohen, Irun R.
Published in Proceedings of the National Academy of Sciences - PNAS (27.04.1999)
Published in Proceedings of the National Academy of Sciences - PNAS (27.04.1999)
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X-linked spondyloepiphyseal dysplasia tarda: A novel SEDL mutation in a Jewish Ashkenazi family and clinical intervention considerations
Bar-Yosef, Udy, Ohana, Eric, Hershkovitz, Eli, Perlmuter, Sarit, Ofir, Rivka, Birk, Ohad S.
Published in American journal of medical genetics. Part A (15.02.2004)
Published in American journal of medical genetics. Part A (15.02.2004)
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Journal Article
Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9
Barel, Ortal, Shalev, Stavit A., Ofir, Rivka, Cohen, Asi, Zlotogora, Joel, Shorer, Zamir, Mazor, Galia, Finer, Gal, Khateeb, Shareef, Zilberberg, Noam, Birk, Ohad S.
Published in American journal of human genetics (01.08.2008)
Published in American journal of human genetics (01.08.2008)
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Journal Article
PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy
Khateeb, Shareef, Flusser, Hagit, Ofir, Rivka, Shelef, Ilan, Narkis, Ginat, Vardi, Gideon, Shorer, Zamir, Levy, Rachel, Galil, Aharon, Elbedour, Khalil, Birk, Ohad S.
Published in American journal of human genetics (01.11.2006)
Published in American journal of human genetics (01.11.2006)
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Journal Article
Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ
Barel, Ortal, Shorer, Zamir, Flusser, Hagit, Ofir, Rivka, Narkis, Ginat, Finer, Gal, Shalev, Hanah, Nasasra, Ahmad, Saada, Ann, Birk, Ohad S.
Published in American journal of human genetics (01.05.2008)
Published in American journal of human genetics (01.05.2008)
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Journal Article
Hsp60 peptide therapy of NOD mouse diabetes induces a Th2 cytokine burst and downregulates autoimmunity to various β-cell antigens
ELIAS, D, MEILIN, A, ABLAMUNITS, V, BIRK, O. S, CARMI, P, KÖNEN-WAISMAN, S, COHEN, I. R
Published in Diabetes (New York, N.Y.) (01.05.1997)
Published in Diabetes (New York, N.Y.) (01.05.1997)
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Journal Article
Lethal Contractural Syndrome Type 3 (LCCS3) Is Caused by a Mutation in PIP5K1C, Which Encodes PIPKIy of the Phophatidylinsitol Pathway
Narkis, G, Oflr, R, Landau, D, Manor, E, Volokita, M, Hershkowitz, R, Elbedour, K, Birk, O S
Published in American journal of human genetics (01.09.2007)
Published in American journal of human genetics (01.09.2007)
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