Overall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers von Golan, T, Kanji, Z S, Epelbaum, R, Devaud, N, Dagan, E, Holter, S, Aderka, D, Paluch-Shimon, S, Kaufman, B, Gershoni-Baruch, R, Hedley, D, Moore, M J, Friedman, E, Gallinger, S

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Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease von Sidransky, E, Nalls, M.A, Aasly, J.O, Aharon-Peretz, J, Annesi, G, Barbosa, E.R, Bar-Shira, A, Berg, D, Bras, J, Brice, A, Chen, C.-M, Clark, L.N, Condroyer, C, De Marco, E.V, Dürr, A, Eblan, M.J, Fahn, S, Farrer, M.J, Fung, H.-C, Gan-Or, Z, Gasser, T, Gershoni-Baruch, R, Giladi, N, Griffith, A, Gurevich, T, Januario, C, Kropp, P, Lang, A.E, Lee-Chen, G.-J, Lesage, S, Marder, K, Mata, I.F, Mirelman, A, Mitsui, J, Mizuta, I, Nicoletti, G, Oliveira, C, Ottman, R, Orr-Urtreger, A, Pereira, L.V, Quattrone, A, Rogaeva, E, Rolfs, A, Rosenbaum, H, Rozenberg, R, Samii, A, Samaddar, T, Schulte, C, Sharma, M, Singleton, A, Spitz, M, Tan, E.-K, Tayebi, N, Toda, T, Troiano, A.R, Tsuji, S, Wittstock, M, Wolfsberg, T.G, Wu, Y.-R, Zabetian, C.P, Zhao, Y, Ziegler, S.G

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Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis von Chinn, Ivan K., Eckstein, Olive S., Peckham-Gregory, Erin C., Goldberg, Baruch R., Forbes, Lisa R., Nicholas, Sarah K., Mace, Emily M., Vogel, Tiphanie P., Abhyankar, Harshal A., Diaz, Maria I., Heslop, Helen E., Krance, Robert A., Martinez, Caridad A., Nguyen, Trung C., Bashir, Dalia A., Goldman, Jordana R., Stray-Pedersen, Asbjørg, Pedroza, Luis A., Poli, M. Cecilia, Aldave-Becerra, Juan C., McGhee, Sean A., Al-Herz, Waleed, Chamdin, Aghiad, Coban-Akdemir, Zeynep H., Jhangiani, Shalini N., Muzny, Donna M., Cao, Tram N., Hong, Diana N., Gibbs, Richard A., Lupski, James R., Orange, Jordan S., McClain, Kenneth L., Allen, Carl E.

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The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews von Dagan, E, Schlesinger, I, Ayoub, M, Mory, A, Nassar, M, Kurolap, A, Peretz-Aharon, J, Gershoni-Baruch, R

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Early onset breast cancer in Ashkenazi women carriers of founder BRCA1/2 mutations: beyond 10 years of follow‐up von Dagan, E., Gershoni‐Baruch, R., Kurolap, A., Fried, G.

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Effects of Online Choir or Mindfulness Interventions on Auditory Perception and Well-Being in Middle- and Older-Aged Adults During the COVID-19 Pandemic: A Randomized Controlled Tr... von Herschel, Ellen, Hennessy, Sarah, Cahn, Baruch R, Goldsworthy, Raymond, Habibi, Assal

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Long-Term Effects of Pregnancy on Renal Graft Function in Women After Kidney Transplantation Compared With Matched Controls von Svetitsky, S., Baruch, R., Schwartz, I.F., Schwartz, D., Nakache, R., Goykhman, Y., Katz, P., Grupper, A.

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Hepatobiliary Dysfunction and Disseminated Intravascular Coagulation Increase Risk of Mortality in Pediatric Hemophagocytic Lymphohistiocytosis von Goldman, Jordana, Desai, Moreshwar S, McClain, Kenneth L, Tcharmtchi, M Hossein, Kennedy, Curtis E, Thompson, Kathleen, Lam, Fong, Bashir, Dalia A, Chinn, Ivan K, Goldberg, Baruch R, Allen, Carl E, Nguyen, Trung C

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IFN-γ signature in the plasma proteome distinguishes pediatric hemophagocytic lymphohistiocytosis from sepsis and SIRS von Lin, Howard, Scull, Brooks P., Goldberg, Baruch R., Abhyankar, Harshal A., Eckstein, Olive E., Zinn, Daniel J., Lubega, Joseph, Agrusa, Jennifer, El Mallawaney, Nader, Gulati, Nitya, Forbes, Lisa, Chinn, Ivan, Chakraborty, Rikhia, Velasquez, Jessica, Goldman, Jordana, Bashir, Dalia, Lam, Fong, Muscal, Eyal, Henry, Michael. M., Greenberg, Jay N., Ladisch, Stephan, Hermiston, Michelle L., Meyer, Lauren K., Jeng, Michael, Naqvi, Ahmed, McClain, Kenneth, Nguyen, Trung, Wong, Hector, Man, Tsz-Kwong, Jordan, Michael B., Allen, Carl E.

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The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers von INZELBERG, R, COHEN, O. S, INZELBERG, L, KAPLAN, N, FIXLER MEHR, T, MORY, A, DAGAN, E, SCHECHTMAN, E, FRIEDMAN, E, HASSIN-BAER, S, AHARON-PERETZ, J, SCHLESINGER, I, GERSHONI-BARUCH, R, DJALDETTI, R, NITSAN, Z, EPHRARY, L, TUNKEL, O, KOZLOVA, E

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A Single Nucleotide Polymorphism in the RAD51 Gene Modifies Cancer Risk in BRCA2 but Not BRCA1 Carriers von Levy-Lahad, E., Lahad, A., Eisenberg, S., Dagan, E., Paperna, T., Kasinetz, L., Catane, R., Kaufman, B., Beller, U., Renbaum, P., Gershoni-Baruch, R.

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Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease von CORMAND, B, PIHKO, H, VOIT, T, TOPALOGLU, H, DOBYNS, W. B, LEHESJOKI, A.-E, BAYES, M, VALANNE, L, SANTAVUORI, P, TALIM, B, GERSHONI-BARUCH, R, AHMAD, A, VAN BOKHOVEN, H, BRUNNER, H. G

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Common presentations of pediatric rheumatologic diseases: a generalist's guide von Reyhan, Iris, Goldberg, Baruch R, Gottlieb, Beth S

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Genetic and Mechanistic Diversity in Hemophagocytic Lymphohistiocytosis von Chinn, Ivan K., Eckstein, Olive S., Peckham-Gregory, Erin C., Goldberg, Baruch R., Forbes, Lisa R., Nicholas, Sarah K., Mace, Emily M., Vogel, Tiphanie P., Abhyankar, Harshal A., Diaz, Maria I., Heslop, Helen E., Krance, Robert A., Martinez, Caridad A., Nguyen, Trung C., Bashir, Dalia A., Goldman, Jordana R., Stray-Pedersen, Asbjorg, Pedroza, Luis A., Poli, M. Cecilia, Aldave Becerra, Juan Carlos, McGhee, Sean A., Coban-Akdemir, Zeynep H., Jhangiani, Shalini N., Muzny, Donna M., Cao, Tram N., Hong, Diana N., Gibbs, Richard A., Lupski, James R., Orange, Jordan S., McClain, Kenneth L., Allen, Carl E.

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BRCA1/2 mutations are not associated with FMR1 genotypes, nor with assisted reproductive performance von Cohen, Y, Raanani, H, Feldman, B, Dagan, E, Meirow, D, Gershoni-Baruch, R

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Breast-feeding and the Risk of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers von Jernström, H., Lubinski, J., Lynch, H. T., Ghadirian, P., Neuhausen, S., Isaacs, C., Weber, B. L., Horsman, D., Rosen, B., Foulkes, W. D., Friedman, E., Gershoni-Baruch, R., Ainsworth, P., Daly, M., Garber, J., Olsson, H., Sun, P., Narod, S. A.

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6632 POSTER BRCA1/2 Mutations in Pancreatic Cancer Patients and Their Clinical Characteristics von Epelbaum, R, Dagan, E, Gershoni-Baruch, R

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SMPD1 mutations and Parkinson disease von Dagan, E, Adir, V, Schlesinger, I, Borochowitz, Z, Ayoub, M, Mory, A, Nassar, M, Kurolap, A, Aharon-Peretz, J, Gershoni-Baruch, R

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PO58 Early onset breast cancer: clinical characteristics and patterns of relapse in BRCA1/2 mutation carriers compared to non-carriers von Fried, G, Matanis, E, Gershoni-Baruch, R, Dagan, E

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Association of the C677T polymorphism in the MTHFR gene with breast and/or ovarian cancer risk in Jewish women von Gershoni-Baruch, R, Dagan, E, Israeli, D, Kasinetz, L, Kadouri, E, Friedman, E

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