RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations von Hershkovitz, D., Bercovich, D., Sprecher, E., Lapidot, M.

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The LRRK2 G2019S mutation in ashkenazi Jews with Parkinson disease : Is there a gender effect? von ORR-URTREGER, A, SHIFRIN, C, ROZOVSKI, U, ROSNER, S, BERCOVICH, D, GUREVICH, T, YAGEV-MORE, H, BAR-SHIRA, A, GILADI, N

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Severe infantile male encephalopathy is a result of early post-zygotic WDR45 somatic mutation von Spiegel, R., Shalev, S., Bercovich, D., Rabinovich, D., Khayat, M., Shaag, A., Elpeleg, O.

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A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia von Solomon-Zemler, R, Basel-Vanagaite, L, Steier, D, Yakar, S, Mel, E, Phillip, M, Bazak, L, Bercovich, D, Werner, H, de Vries, L

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The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation von Basel-Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M

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A Mutation Analysis of the Phenylalanine Hydroxylase (PAH) Gene in the Israeli Population von Bercovich, D., Elimelech, A., Yardeni, T., Korem, S., Zlotogora, J., Gal, N., Goldstein, N., Vilensky, B., Segev, R., Avraham, S., Loewenthal, R., Schwartz, G., Anikster, Y.

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SFB-based S-haplotyping of apricot (Prunus armeniaca) with DHPLC von Raz, A, Stern, R.A, Bercovich, D, Goldway, M

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Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome von Bercovich, Dani, PhD, Ganmore, Ithamar, BMedSc, Scott, Linda M, PhD, Wainreb, Gilad, MSc, Birger, Yehudit, PhD, Elimelech, Arava, MSc, Shochat, Chen, MSc, Cazzaniga, Giovanni, PhD, Biondi, Andrea, MD, Basso, Giuseppe, Prof, Cario, Gunnar, MD, Schrappe, Martin, Prof, Stanulla, Martin, Prof, Strehl, Sabine, PhD, Haas, Oskar A, Prof, Mann, Georg, MD, Binder, Vera, MD, Borkhardt, Arndt, Prof, Kempski, Helena, PhD, Trka, Jan, Prof, Bielorei, Bella, MD, Avigad, Smadar, PhD, Stark, Batia, Prof, Smith, Owen, Prof, Dastugue, Nicole, PhD, Bourquin, Jean-Pierre, MD, Tal, Nir Ben, Prof, Green, Anthony R, Prof, Izraeli, Shai, Prof

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A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ich... von Sprecher, Eli, Ishida-Yamamoto, Akemi, Mizrahi-Koren, Mordechai, Rapaport, Debora, Goldsher, Dorit, Indelman, Margarita, Topaz, Orit, Chefetz, Ilana, Keren, Hanni, O’Brien, Timothy J., Bercovich, Dani, Shalev, Stavit, Geiger, Dan, Bergman, Reuven, Horowitz, Mia, Mandel, Hanna

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Characterization of the human β4 nAChR gene and polymorphisms in CHRNA3 and CHRNB4 von Lev-Lehman, E., Bercovich, D., Xu, W., Stockton, D. W., Beaudet, A. L.

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A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis von Topaz, Orit, Indelman, Margarita, Chefetz, Ilana, Geiger, Dan, Metzker, Aryeh, Altschuler, Yoram, Choder, Mordechai, Bercovich, Dani, Uitto, Jouni, Bergman, Reuven, Richard, Gabriele, Sprecher, Eli

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Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21 von Rainis, Liat, Bercovich, Dan, Strehl, Sabine, Teigler-Schlegel, Andrea, Stark, Batia, Trka, Jan, Amariglio, Ninette, Biondi, Andrea, Muler, Inna, Rechavi, Gideon, Kempski, Helena, Haas, Oskar A., Izraeli, Shai

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Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14 von Lugassy, Jennie, Itin, Peter, Ishida-Yamamoto, Akemi, Holland, Kristen, Huson, Susan, Geiger, Dan, Hennies, Hans Christian, Indelman, Margarita, Bercovich, Dani, Uitto, Jouni, Bergman, Reuven, McGrath, John A., Richard, Gabriele, Sprecher, Eli

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Case Study: A Human Pre-Natal Experiment in 1944—“Do No Harm” von Bercovich, D., Shlush, K., Goodman, G.

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Mitochondrial pro-apoptotic ARTS protein is lost in the majority of acute lymphoblastic leukemia patients von Elhasid, Ronit, Sahar, Dvora, Merling, Ayellet, Zivony, Yifat, Rotem, Asaf, Ben-Arush, Miriam, Izraeli, Shai, Bercovich, Dani, Larisch, Sarit

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A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A von Jiang, Yong-hui, Sahoo, Trilochan, Michaelis, Ron C., Bercovich, Dani, Bressler, Jan, Kashork, Catherine D., Liu, Qian, Shaffer, Lisa G., Schroer, Richard J., Stockton, David W., Spielman, Richard S., Stevenson, Roger E., Beaudet, Arthur L.

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Central role of alpha 7 nicotinic receptor in differentiation of the stratified squamous epithelium von Arredondo, J, Nguyen, Vu Thuong, Chernyavsky, AI, Bercovich, D, Orr-Urtreger, A, Kummer, W, Lips, K, Vetter, DE, Grando, SA

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A Novel Founder Mutation in the RNASEL Gene, 471delAAAG, Is Associated with Prostate Cancer in Ashkenazi Jews von Rennert, Hanna, Bercovich, Dani, Hubert, Ayala, Abeliovich, Dvora, Rozovsky, Uri, Bar-Shira, Anat, Soloviov, Sonya, Schreiber, Letizia, Matzkin, Haim, Rennert, Gad, Kadouri, Luna, Peretz, Tamar, Yaron, Yuval, Orr-Urtreger, Avi

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Synergistic control of keratinocyte adhesion through muscarinic and nicotinic acetylcholine receptor subtypes von Nguyen, Vu Thuong, Chernyavsky, Alexander I, Arredondo, Juan, Bercovich, Dani, Orr-Urtreger, Avi, Vetter, Douglas E, Wess, Jürgen, Beaudet, Arthur L, Kitajima, Yasuo, Grando, Sergei A

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High Frequency of BRCA 1/2 Mutations Among Israeli Non Ashkenazi Breast Cancer Patients von Elyan, F., Maimon, O., Salah, A.F., Sagi, M., Kaduri, L., Lerer, I., Goldberg, Y., Hamburger, T., Bercovich, D., Peretz-Yablonski, T.

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