Torthaí cuardaigh - Tzur, Shay

Big data analysis of human mitochondrial DNA substitution models: a regression approach de réir Levinstein Hallak, Keren, Tzur, Shay, Rosset, Saharon

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Linkage disequilibrium analysis reveals an albuminuria risk haplotype containing three missense mutations in the cubilin gene with striking differences among European and African a... de réir Tzur, Shay, Wasser, Walter G, Rosset, Saharon, Skorecki, Karl

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Exome sequencing identified mutations in CASK and MYBPC3 as the cause of a complex dilated cardiomyopathy phenotype de réir REINSTEIN, EYAL, TZUR, SHAY, BORMANS, CONCETTA, BEHAR, DORON M.

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Germline variant in REXO2 is a novel candidate gene in familial pheochromocytoma de réir Laitman, Yael, Tzur, Shay, Attai, Ruben, Tirosh, Amit, Friedman, Eitan

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Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing de réir Reinstein, Eyal, Tzur, Shay, Cohen, Rony, Bormans, Concetta, Behar, Doron M

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Exome sequencing identified a novel de novo OPA1 mutation in a consanguineous family presenting with optic atrophy de réir COHEN, LIOR, TZUR, SHAY, GOLDENBERG-COHEN, NITZA, BORMANS, CONCETTA, BEHAR, DORON M., REINSTEIN, EYAL

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Adaptation of Pelage Color and Pigment Variations in Israeli Subterranean Blind Mole Rats, Spalax Ehrenbergi de réir Singaravelan, Natarajan, Raz, Shmuel, Tzur, Shay, Belifante, Shirli, Pavlicek, Tomas, Beiles, Avigdor, Ito, Shosuke, Wakamatsu, Kazumasa, Nevo, Eviatar

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Correction: Adaptation of Pelage Color and Pigment Variations in Israeli Subterranean Blind Mole Rats, Spalax Ehrenbergi de réir Singaravelan, Natarajan, Raz, Shmuel, Tzur, Shay, Belifante, Shirli, Pavlicek, Tomas, Beiles, Avigdor, Ito, Shosuke, Wakamatsu, Kazumasa, Nevo, Eviatar

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Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation de réir Shohet, Adi, Cohen, Lior, Haguel, Danielle, Mozer, Yael, Shomron, Noam, Tzur, Shay, Bazak, Lily, Basel Salmon, Lina, Krause, Irit

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Possible incipient sympatric ecological speciation in blind mole rats (Spalax) de réir Hadid, Yarin, Tzur, Shay, Pavlíček, Tomáš, Šumbera, Radim, Šklíba, Jan, Lövy, Matěj, Fragman-Sapir, Ori, Beiles, Avigdor, Arieli, Ran, Raz, Shmuel, Nevo, Eviatar

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Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene de réir Tzur, Shay, Rosset, Saharon, Shemer, Revital, Yudkovsky, Guennady, Selig, Sara, Tarekegn, Ayele, Bekele, Endashaw, Bradman, Neil, Wasser, Walter G., Behar, Doron M., Skorecki, Karl

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APOL1 Risk Variants Predict Histopathology and Progression to ESRD in HIV-Related Kidney Disease de réir Fine, Derek M., Wasser, Walter G., Estrella, Michelle M., Atta, Mohamed G., Kuperman, Michael, Shemer, Revital, Rajasekaran, Arun, Tzur, Shay, Racusen, Lorraine C., Skorecki, Karl

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The Genographic Project Public Participation Mitochondrial DNA Database de réir Behar, Doron M, Rosset, Saharon, Blue-Smith, Jason, Balanovsky, Oleg, Tzur, Shay, Comas, David, Mitchell, R. John, Quintana-Murci, Lluis, Tyler-Smith, Chris, Wells, R. Spencer

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Correction: The Genographic Project Public Participation Mitochondrial DNA Database de réir M. Behar, Doron, Rosset, Saharon, Blue-Smith, Jason, Balanovsky, Oleg, Tzur, Shay, Comas, David, Mitchell, R. John, Quintana-Murci, Lluis, Tyler-Smith, Chris, Wells, R. Spencer

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A Novel 154-bp Deletion in the Human Mitochondrial DNA Control Region in Healthy Individuals de réir Behar, Doron M., Blue-Smith, Jason, Soria-Hernanz, David F., Tzur, Shay, Hadid, Yarin, Bormans, Concetta, Moen, Alexander, Tyler-Smith, Chris, Quintana-Murci, Lluis, Wells, R. Spencer

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African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans de réir Behar, Doron M., Rosset, Saharon, Tzur, Shay, Selig, Sara, Yudkovsky, Guennady, Bercovici, Sivan, Kopp, Jeffrey B., Winkler, Cheryl A., Nelson, George W., Wasser, Walter G., Skorecki, Karl

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Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency de réir Behar, Doron M., Basel-Vanagaite, Lina, Glaser, Fabian, Kaplan, Marielle, Tzur, Shay, Magal, Nurit, Eidlitz-Markus, Tal, Haimi-Cohen, Yishay, Sarig, Galit, Bormans, Concetta, Shohat, Mordechai, Zeharia, Avraham

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Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora de réir Behar, Doron M., Metspalu, Ene, Kivisild, Toomas, Rosset, Saharon, Tzur, Shay, Hadid, Yarin, Yudkovsky, Guennady, Rosengarten, Dror, Pereira, Luisa, Amorim, Antonio, Kutuev, Ildus, Gurwitz, David, Bonne-Tamir, Batsheva, Villems, Richard, Skorecki, Karl

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Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C de réir Reinstein, Eyal, Gutierrez-Fernandez, Ana, Tzur, Shay, Bormans, Concetta, Marcu, Shai, Tayeb-Fligelman, Einav, Vinkler, Chana, Raas-Rothschild, Annick, Irge, Dana, Landau, Meytal, Shohat, Mordechai, Puente, Xose S, Behar, Doron M, Lopez-Otın, Carlos

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The Dawn of Human Matrilineal Diversity de réir Behar, Doron M., Villems, Richard, Soodyall, Himla, Blue-Smith, Jason, Pereira, Luisa, Metspalu, Ene, Scozzari, Rosaria, Makkan, Heeran, Tzur, Shay, Comas, David, Bertranpetit, Jaume, Quintana-Murci, Lluis, Tyler-Smith, Chris, Wells, R. Spencer, Rosset, Saharon

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