Clonal evolution of leukemia from G6PD studies

por Bacharach, Tal, Shlush, Liran I.
Publicado 2023

Evolutionary trajectory of leukemic clones and its clinical implications

por Tuval, Amos, Shlush, Liran I
Publicado 2019

Ashkenazi Jewish Centenarians Do Not Demonstrate Enrichment in Mitochondrial Haplogroup J

por Shlush, Liran I., Atzmon, Gil, Weisshof, Roni, Behar, Doron, Yudkovsky, Guenady, Barzilai, Nir, Skorecki, Karl
Publicado 2008

Admixture mapping of end stage kidney disease genetic susceptibility using estimated mutual information ancestry informative markers

por Shlush, Liran I, Bercovici, Sivan, Wasser, Walter G, Yudkovsky, Guennady, Templeton, Alan, Geiger, Dan, Skorecki, Karl
Publicado 2010

Comparing Algorithms That Reconstruct Cell Lineage Trees Utilizing Information on Microsatellite Mutations

por Chapal-Ilani, Noa, Maruvka, Yosef E., Spiro, Adam, Reizel, Yitzhak, Adar, Rivka, Shlush, Liran I., Shapiro, Ehud
Publicado 2013

Quantitative digital in situ senescence-associated β-galactosidase assay

por Shlush, Liran I, Itzkovitz, Shalev, Cohen, Ariel, Rutenberg, Aviad, Berkovitz, Ron, Yehezkel, Shiran, Shahar, Hofit, Selig, Sara, Skorecki, Karl
Publicado 2011

The Druze: A Population Genetic Refugium of the Near East

por Shlush, Liran I., Behar, Doron M., Yudkovsky, Guennady, Templeton, Alan, Hadid, Yarin, Basis, Fuad, Hammer, Michael, Itzkovitz, Shalev, Skorecki, Karl
Publicado 2008

SmMIP-tools: a computational toolset for processing and analysis of single-molecule molecular inversion probes-derived data

por Medeiros, Jessie J F, Capo-Chichi, Jose-Mario, Shlush, Liran I, Dick, John E, Arruda, Andrea, Minden, Mark D, Abelson, Sagi
Publicado 2022

Colon Stem Cell and Crypt Dynamics Exposed by Cell Lineage Reconstruction

por Reizel, Yitzhak, Chapal-Ilani, Noa, Adar, Rivka, Itzkovitz, Shalev, Elbaz, Judith, Maruvka, Yosef E., Segev, Elad, Shlush, Liran I., Dekel, Nava, Shapiro, Ehud
Publicado 2011

High efficiency error suppression for accurate detection of low-frequency variants

por Wang, Ting Ting, Abelson, Sagi, Zou, Jinfeng, Li, Tiantian, Zhao, Zhen, Dick, John E, Shlush, Liran I, Pugh, Trevor J, Bratman, Scott V
Publicado 2019

Pseudo-mutant P53 is a unique phenotype of DNMT3A-mutated pre-leukemia

por Tuval, Amos, Brilon, Yardena, Azogy, Hadas, Moskovitz, Yoni, Leshkowitz, Dena, Salame, Tomer M, Minden, Mark D, Tal, Perry, Rotter, Varda, Oren, Moshe, Kaushansky, Nathali, Shlush, Liran I
Publicado 2022

Dasatinib response in acute myeloid leukemia is correlated with FLT3/ITD, PTPN11 mutations and a unique gene expression signature

por Tavor, Sigal, Shalit, Tali, Ilani, Noa Chapal, Moskovitz, Yoni, Livnat, Nir, Groner, Yoram, Barr, Haim, Minden, Mark D., Plotnikov, Alexander, Deininger, Michael W., Kaushansky, Nathali, Shlush, Liran I.
Publicado 2020

Recurrent deletions in clonal hematopoiesis are driven by microhomology-mediated end joining

por Feldman, Tzah, Bercovich, Akhiad, Moskovitz, Yoni, Chapal-Ilani, Noa, Mitchell, Amanda, Medeiros, Jessie J. F., Biezuner, Tamir, Kaushansky, Nathali, Minden, Mark D., Gupta, Vikas, Milyavsky, Michael, Livneh, Zvi, Tanay, Amos, Shlush, Liran I.
Publicado 2021

Cardiovascular Disease Among Patients With AML and CHIP-Related Mutations

por Calvillo-Argüelles, Oscar, Schoffel, Alice, Capo-Chichi, José-Mario, Abdel-Qadir, Husam, Schuh, Andre, Carrillo-Estrada, Montserrat, Liu, Shiying, Gupta, Vikas, Schimmer, Aaron D., Yee, Karen, Shlush, Liran I., Natarajan, Pradeep, Thavendiranathan, Paaladinesh
Publicado 2022

Integration of intra-sample contextual error modeling for improved detection of somatic mutations from deep sequencing

por Abelson, Sagi, Zeng, Andy G. X., Nofech-Mozes, Ido, Wang, Ting Ting, Ng, Stanley W. K., Minden, Mark D., Pugh, Trevor J., Awadalla, Philip, Shlush, Liran I., Murphy, Tracy, Chan, Steven M., Dick, John E., Bratman, Scott V.
Publicado 2020

Inflammatory signals from fatty bone marrow support DNMT3A driven clonal hematopoiesis

por Zioni, N., Bercovich, A. Akhiad, Chapal-Ilani, N., Bacharach, Tal, Rappoport, N., Solomon, A., Avraham, R., Kopitman, E., Porat, Z., Sacma, M., Hartmut, G., Scheller, M., Muller-Tidow, C., Lipka, D., Shlush, E., Minden, M., Kaushansky, N., Shlush, Liran I.
Publicado 2023

Donor cell leukemia: is reappearance of gene mutations in donor cells more than an incidental phenomenon?

por Gabay, Tal Shahar, Chapal-Ilani, Noa, Moskovitz, Yoni, Biezuner, Tamir, Oron, Barak, Brilon, Yardena, Fridman-Dror, Anna, Sabah, Rawan, Balicer, Ran, Tanay, Amos, Mendelson-Cohen, Netta, Dann, Eldad J., Fineman, Riva, Kaushansky, Nathali, Yehudai-Reshef, Shlomit, Zuckerman, Tsila, Shlush, Liran I.
Publicado 2020

An improved molecular inversion probe based targeted sequencing approach for low variant allele frequency

por Biezuner, Tamir, Brilon, Yardena, Arye, Asaf Ben, Oron, Barak, Kadam, Aditee, Danin, Adi, Furer, Nili, Minden, Mark D, Hwan Kim, Dennis Dong, Shapira, Shiran, Arber, Nadir, Dick, John, Thavendiranathan, Paaladinesh, Moskovitz, Yoni, Kaushansky, Nathali, Chapal-Ilani, Noa, Shlush, Liran I
Publicado 2022

Clonal hematopoiesis in the donor does not adversely affect long-term outcomes following allogeneic hematopoietic stem cell transplantation: result from a 13-year follow-up

por Kim, Kyoung Ha, Kim, TaeHyung, Novitzky-Basso, Igor, Lee, Hyewon, Yoo, Youngseok, Ahn, Jae-Sook, Pasic, Ivan, Law, Arjun, Lam, Wilson, Michelis, Fotios V., Gerbitz, Armin, Viswabandya, Auro, Lipton, Jeffrey, Kumar, Rajat, Mattsson, Jonas, Zhang, Zhaolei, Kaushansky, Nathali, Brilon, Yardena, Chapal-Ilani, Noa, Biezuner, Tamir, Shlush, Liran I., Kim, Dennis Dong Hwan
Publicado 2023

Identification of pre-leukemic hematopoietic stem cells in acute leukemia

por Shlush, Liran I., Zandi, Sasan, Mitchell, Amanda, Chen, Weihsu Claire, Brandwein, Joseph M., Gupta, Vikas, Kennedy, James A., Schimmer, Aaron D., Schuh, Andre C., Yee, Karen W., McLeod, Jessica L., Doedens, Monica, Medeiros, Jessie J.F., Marke, Rene, Kim, Hyeoung Joon, Lee, Kwon, McPherson, John D., Hudson, Thomas J., Brown, Andrew M.K., Trinh, Quang M., Stein, Lincoln D., Minden, Mark D., Wang, Jean C.Y., Dick, John E.
Publicado 2014