Essential Tremor Prevalence is Low in the Druze Population in Northern Israel

Por Aharon-peretz, Judith, Badarny, Samih, Ibrahim, Raphiq, Gershoni-baruch, Ruth, Hassoun, Gamal
Publicado em 2012

A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred

Por Mory, Adi, Ruiz, Francesc X, Dagan, Efrat, Yakovtseva, Evgenia A, Kurolap, Alina, Parés, Xavier, Farrés, Jaume, Gershoni-Baruch, Ruth
Publicado em 2014

Offspring Gender Ratio and the Rate of Recurrent Spontaneous Miscarriages in Jewish Women at High Risk for Breast/Ovarian Cancer

Por Gal, Inbar, Sadetzki, Siegal, Gershoni-Baruch, Ruth, Oberman, Bernice, Carp, Howard, Papa, Moshe Z., Diestelman-Menachem, Tal, Eisenberg-Barzilai, Shlomit, Friedman, Eitan
Publicado em 2004

BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control study

Por Dagan, Efrat, Cohen, Yoram, Mory, Adi, Adir, Vardit, Borochowitz, Zvi, Raanani, Hila, Kurolap, Alina, Melikhan-Revzin, Svetlana, Meirow, Dror, Gershoni-Baruch, Ruth
Publicado em 2014

BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control study

Por Dagan, Efrat, Cohen, Yoram, Mory, Adi, Adir, Vardit, Borochowitz, Zvi, Raanani, Hila, Kurolap, Alina, Melikhan-Revzin, Svetlana, Meirow, Dror, Gershoni-Baruch, Ruth
Publicado em 2014

SERKAL Syndrome: An Autosomal-Recessive Disorder Caused by a Loss-of-Function Mutation in WNT4

Por Mandel, Hannah, Shemer, Revital, Borochowitz, Zvi U., Okopnik, Marina, Knopf, Carlos, Indelman, Margarita, Drugan, Arie, Tiosano, Dov, Gershoni-Baruch, Ruth, Choder, Mordechai, Sprecher, Eli
Publicado em 2008

Latitudinal Clines of the Human Vitamin D Receptor and Skin Color Genes

Por Tiosano, Dov, Audi, Laura, Climer, Sharlee, Zhang, Weixiong, Templeton, Alan R., Fernández-Cancio, Monica, Gershoni-Baruch, Ruth, Sánchez-Muro, José Miguel, El Kholy, Mohamed, Hochberg, Zèev
Publicado no G3 (Bethesda) (2016)

A Nonsense Mutation in the Human Homolog of Drosophila rogdi Causes Kohlschutter–Tonz Syndrome

Por Mory, Adi, Dagan, Efrat, Illi, Barbara, Duquesnoy, Philippe, Mordechai, Shikma, Shahor, Ishai, Romani, Sveva, Hawash-Moustafa, Nivin, Mandel, Hanna, Valente, Enza M., Amselem, Serge, Gershoni-Baruch, Ruth
Publicado em 2012

Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy

Por Magen, Daniella, Georgopoulos, Costa, Bross, Peter, Ang, Debbie, Segev, Yardena, Goldsher, Dorit, Nemirovski, Alexandra, Shahar, Eli, Ravid, Sarit, Luder, Anthony, Heno, Bayan, Gershoni-Baruch, Ruth, Skorecki, Karl, Mandel, Hanna
Publicado em 2008

Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3

Por Lorenz-Depiereux, Bettina, Benet-Pages, Anna, Eckstein, Gertrud, Tenenbaum-Rakover, Yardena, Wagenstaller, Janine, Tiosano, Dov, Gershoni-Baruch, Ruth, Albers, Norbert, Lichtner, Peter, Schnabel, Dirk, Hochberg, Ze’ev, Strom, Tim M.
Publicado em 2006

Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population

Por Simchoni, Sharon, Friedman, Eitan, Kaufman, Bella, Gershoni-Baruch, Ruth, Orr-Urtreger, Avi, Kedar-Barnes, Inbal, Shiri-Sverdlov, Ronit, Dagan, Efrat, Tsabari, Sigal, Shohat, Mordechai, Catane, Raphael, King, Mary-Claire, Lahad, Amnon, Levy-Lahad, Ephrat
Publicado em 2006

Haplotype analysis of the 185delAG BRCA1 mutation in ethnically diverse populations

Por Laitman, Yael, Feng, Bing-Jian, Zamir, Itay M, Weitzel, Jeffrey N, Duncan, Paul, Port, Danielle, Thirthagiri, Eswary, Teo, Soo-Hwang, Evans, Gareth, Latif, Ayse, Newman, William G, Gershoni-Baruch, Ruth, Zidan, Jamal, Shimon-Paluch, Shani, Goldgar, David, Friedman, Eitan
Publicado em 2013

Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers

Por Friedman, Eitan, Kotsopoulos, Joanne, Lubinski, Jan, Lynch, Henry T, Ghadirian, Parviz, Neuhausen, Susan L, Isaacs, Claudine, Weber, Barbara, Foulkes, William D, Moller, Pal, Rosen, Barry, Kim-Sing, Charmaine, Gershoni-Baruch, Ruth, Ainsworth, Peter, Daly, Mary, Tung, Nadine, Eisen, Andrea, Olopade, Olufunmilayo I, Karlan, Beth, Saal, Howard M, Garber, Judy E, Rennert, Gad, Gilchrist, Dawna, Eng, Charis, Offit, Kenneth, Osborne, Michael, Sun, Ping, Narod, Steven A
Publicado em 2006

EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy

Por Byrne, Susan, Jansen, Lara, U-King-Im, Jean-Marie, Siddiqui, Ata, Lidov, Hart G. W., Bodi, Istvan, Smith, Luke, Mein, Rachael, Cullup, Thomas, Dionisi-Vici, Carlo, Al-Gazali, Lihadh, Al-Owain, Mohammed, Bruwer, Zandre, Al Thihli, Khalid, El-Garhy, Rana, Flanigan, Kevin M., Manickam, Kandamurugu, Zmuda, Erik, Banks, Wesley, Gershoni-Baruch, Ruth, Mandel, Hanna, Dagan, Efrat, Raas-Rothschild, Annick, Barash, Hila, Filloux, Francis, Creel, Donnell, Harris, Michael, Hamosh, Ada, Kölker, Stefan, Ebrahimi-Fakhari, Darius, Hoffmann, Georg F., Manchester, David, Boyer, Philip J., Manzur, Adnan Y., Lourenco, Charles Marques, Pilz, Daniela T., Kamath, Arveen, Prabhakar, Prab, Rao, Vamshi K., Rogers, R. Curtis, Ryan, Monique M., Brown, Natasha J., McLean, Catriona A., Said, Edith, Schara, Ulrike, Stein, Anja, Sewry, Caroline, Travan, Laura, Wijburg, Frits A., Zenker, Martin, Mohammed, Shehla, Fanto, Manolis, Gautel, Mathias, Jungbluth, Heinz
Publicado no Brain (2016)

Multi-center analysis of glucocerebrosidase mutations in Parkinson disease

Por Sidransky, Ellen, Nalls, Michael A., Aasly, Jan O., Aharon-Peretz, Judith, Annesi, Grazia, Barbosa, Egberto Reis, Bar-Shira, Anat, Berg, Daniela, Bras, Jose, Brice, Alexis, Chen, Chiung-Mei, Clark, Lorraine N., Condroyer, Christel, De Marco, Elvira Valeria, Dürr, Alexandra, Eblan, Michael J., Fahn, Stanley, Farrer, Matthew, Fung, Hon-Chung, Gan-Or, Ziv, Gasser, Thomas, Gershoni-Baruch, Ruth, Giladi, Nir, Griffith, Alida, Gurevich, Tanya, Januario, Cristina, Kropp, Peter, Lang, Anthony E., Lee-Chen, Guey-Jen, Lesage, Suzanne, Marder, Karen, Mata, Ignacio F., Mirelman, Anat, Mitsui, Jun, Mizuta, Ikuko, Nicoletti, Giuseppe, Oliveira, Catarina, Ottman, Ruth, Orr-Urtreger, Avi, Pereira, Lygia V., Quattrone, Aldo, Rogaeva, Ekaterina, Rolfs, Arndt, Rosenbaum, Hanna, Rozenberg, Roberto, Samii, Ali, Samaddar, Ted, Schulte, Claudia, Sharma, Manu, Singleton, Andrew, Spitz, Mariana, Tan, Eng-King, Tayebi, Nahid, Toda, Tatsushi, Troiano, André, Tsuji, Shoji, Wittstock, Matthias, Wolfsberg, Tyra G., Wu, Yih-Ru, Zabetian, Cyrus P., Zhao, Yi, Ziegler, Shira G.
Publicado em 2009