A citation-based method for searching scientific literature

Qian Wang, Huiying Qiu, Hui Jiang, Lili Wu, Shasha Dong, Jinlan Pan, Wenjuan Wang, Nana Ping, Jing Xia, Aining Sun, Depei Wu, Yongquan Xue, Hans G Drexler, Roderick A F Macleod, Suning Chen. Haematologica 2011
Times Cited: 56







List of co-cited articles
412 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


PHF6 mutations in T-cell acute lymphoblastic leukemia.
Pieter Van Vlierberghe, Teresa Palomero, Hossein Khiabanian, Joni Van der Meulen, Mireia Castillo, Nadine Van Roy, Barbara De Moerloose, Jan Philippé, Sara González-García, María L Toribio,[...]. Nat Genet 2010
213
66

PHF6 mutations in adult acute myeloid leukemia.
P Van Vlierberghe, J Patel, O Abdel-Wahab, C Lobry, C V Hedvat, M Balbin, C Nicolas, A R Payer, H F Fernandez, M S Tallman,[...]. Leukemia 2011
114
41

Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome.
Karen M Lower, Gillian Turner, Bronwyn A Kerr, Katherine D Mathews, Marie A Shaw, Agi K Gedeon, Susan Schelley, H Eugene Hoyme, Susan M White, Martin B Delatycki,[...]. Nat Genet 2002
153
33

Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia.
Andrew P Weng, Adolfo A Ferrando, Woojoong Lee, John P Morris, Lewis B Silverman, Cheryll Sanchez-Irizarry, Stephen C Blacklow, A Thomas Look, Jon C Aster. Science 2004
28

The genetic basis of early T-cell precursor acute lymphoblastic leukaemia.
Jinghui Zhang, Li Ding, Linda Holmfeldt, Gang Wu, Sue L Heatley, Debbie Payne-Turner, John Easton, Xiang Chen, Jianmin Wang, Michael Rusch,[...]. Nature 2012
26

PHF6 regulates cell cycle progression by suppressing ribosomal RNA synthesis.
Jiadong Wang, Justin Wai-chung Leung, Zihua Gong, Lin Feng, Xiaobing Shi, Junjie Chen. J Biol Chem 2013
65
25

PHF6 interacts with the nucleosome remodeling and deacetylation (NuRD) complex.
Matthew A M Todd, David J Picketts. J Proteome Res 2012
63
23

Prognostic relevance of integrated genetic profiling in acute myeloid leukemia.
Jay P Patel, Mithat Gönen, Maria E Figueroa, Hugo Fernandez, Zhuoxin Sun, Janis Racevskis, Pieter Van Vlierberghe, Igor Dolgalev, Sabrena Thomas, Olga Aminova,[...]. N Engl J Med 2012
19

Gene expression signatures define novel oncogenic pathways in T cell acute lymphoblastic leukemia.
Adolfo A Ferrando, Donna S Neuberg, Jane Staunton, Mignon L Loh, Christine Huard, Susana C Raimondi, Fred G Behm, Ching Hon Pui, James R Downing, D Gary Gilliland,[...]. Cancer Cell 2002
798
19

The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia.
Pieter Van Vlierberghe, Martine van Grotel, Joëlle Tchinda, Charles Lee, H Berna Beverloo, Peter J van der Spek, Andrew Stubbs, Jan Cools, Kyosuke Nagata, Maarten Fornerod,[...]. Blood 2008
161
19

The molecular profile of adult T-cell acute lymphoblastic leukemia: mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL.
Vera Grossmann, Claudia Haferlach, Sandra Weissmann, Andreas Roller, Sonja Schindela, Franziska Poetzinger, Kathrin Stadler, Frauke Bellos, Wolfgang Kern, Torsten Haferlach,[...]. Genes Chromosomes Cancer 2013
116
19

A genome-scale in vivo loss-of-function screen identifies Phf6 as a lineage-specific regulator of leukemia cell growth.
Corbin E Meacham, Lee N Lawton, Yadira M Soto-Feliciano, Justin R Pritchard, Brian A Joughin, Tobias Ehrenberger, Nina Fenouille, Johannes Zuber, Richard T Williams, Richard A Young,[...]. Genes Dev 2015
44
25


The X-linked intellectual disability protein PHF6 associates with the PAF1 complex and regulates neuronal migration in the mammalian brain.
Chi Zhang, Luis A Mejia, Ju Huang, Pamela Valnegri, Eric J Bennett, Julius Anckar, Arezu Jahani-Asl, Gilbert Gallardo, Yoshiho Ikeuchi, Tomoko Yamada,[...]. Neuron 2013
68
17

A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL).
Konstantinos J Mavrakis, Joni Van Der Meulen, Andrew L Wolfe, Xiaoping Liu, Evelien Mets, Tom Taghon, Aly A Khan, Manu Setty, Pieter Rondou, Peter Vandenberghe,[...]. Nat Genet 2011
212
16

T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6.
Mwe Mwe Chao, Matthew A Todd, Udo Kontny, Katherine Neas, Michael J Sullivan, Alasdair G Hunter, David J Picketts, Christian P Kratz. Pediatr Blood Cancer 2010
35
25

ETV6 mutations in early immature human T cell leukemias.
Pieter Van Vlierberghe, Alberto Ambesi-Impiombato, Arianne Perez-Garcia, J Erika Haydu, Isaura Rigo, Michael Hadler, Valeria Tosello, Giusy Della Gatta, Elisabeth Paietta, Janis Racevskis,[...]. J Exp Med 2011
139
16

Oncogenic IL7R gain-of-function mutations in childhood T-cell acute lymphoblastic leukemia.
Priscila P Zenatti, Daniel Ribeiro, Wenqing Li, Linda Zuurbier, Milene C Silva, Maddalena Paganin, Julia Tritapoe, Julie A Hixon, André B Silveira, Bruno A Cardoso,[...]. Nat Genet 2011
276
16

Early T-cell precursor leukaemia: a subtype of very high-risk acute lymphoblastic leukaemia.
Elaine Coustan-Smith, Charles G Mullighan, Mihaela Onciu, Frederick G Behm, Susana C Raimondi, Deqing Pei, Cheng Cheng, Xiaoping Su, Jeffrey E Rubnitz, Giuseppe Basso,[...]. Lancet Oncol 2009
583
16

Gene mutation profiles and prognostic implications in Korean patients with T-lymphoblastic leukemia.
Hee Jae Huh, Soo Hyun Lee, Keon Hee Yoo, Ki Woong Sung, Hong Hoe Koo, Jun Ho Jang, Kihyun Kim, Seok Jin Kim, Won Seog Kim, Chul Won Jung,[...]. Ann Hematol 2013
19
47

PHF6 regulates phenotypic plasticity through chromatin organization within lineage-specific genes.
Yadira M Soto-Feliciano, Jordan M E Bartlebaugh, Yunpeng Liu, Francisco J Sánchez-Rivera, Arjun Bhutkar, Abraham S Weintraub, Jason D Buenrostro, Christine S Cheng, Aviv Regev, Tyler E Jacks,[...]. Genes Dev 2017
31
29

Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia.
Elisabetta Flex, Valentina Petrangeli, Lorenzo Stella, Sabina Chiaretti, Tekla Hornakova, Laurent Knoops, Cristina Ariola, Valentina Fodale, Emmanuelle Clappier, Francesca Paoloni,[...]. J Exp Med 2008
253
14

Activating NOTCH1 mutations predict favorable early treatment response and long-term outcome in childhood precursor T-cell lymphoblastic leukemia.
Stephen Breit, Martin Stanulla, Thomas Flohr, Martin Schrappe, Wolf-Dieter Ludwig, Gabriele Tolle, Margit Happich, Martina U Muckenthaler, Andreas E Kulozik. Blood 2006
192
14

Structural and functional insights into the human Börjeson-Forssman-Lehmann syndrome-associated protein PHF6.
Zhonghua Liu, Fudong Li, Ke Ruan, Jiahai Zhang, Yide Mei, Jihui Wu, Yunyu Shi. J Biol Chem 2014
43
18

Phf6 Loss Enhances HSC Self-Renewal Driving Tumor Initiation and Leukemia Stem Cell Activity in T-ALL.
Agnieszka A Wendorff, S Aidan Quinn, Marissa Rashkovan, Chioma J Madubata, Alberto Ambesi-Impiombato, Mark R Litzow, Martin S Tallman, Elisabeth Paietta, Maddalena Paganin, Giuseppe Basso,[...]. Cancer Discov 2019
36
22

Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity.
Anne K Voss, Robin Gamble, Caitlin Collin, Cheryl Shoubridge, Mark Corbett, Jozef Gécz, Tim Thomas. Gene Expr Patterns 2007
36
19

Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia.
Maria Kleppe, Idoya Lahortiga, Tiama El Chaar, Kim De Keersmaecker, Nicole Mentens, Carlos Graux, Katrien Van Roosbroeck, Adolfo A Ferrando, Anton W Langerak, Jules P P Meijerink,[...]. Nat Genet 2010
132
12

Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia.
Kim De Keersmaecker, Zeynep Kalender Atak, Ning Li, Carmen Vicente, Stephanie Patchett, Tiziana Girardi, Valentina Gianfelici, Ellen Geerdens, Emmanuelle Clappier, Michaël Porcu,[...]. Nat Genet 2013
284
12

Toward a NOTCH1/FBXW7/RAS/PTEN-based oncogenetic risk classification of adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study.
Amélie Trinquand, Aline Tanguy-Schmidt, Raouf Ben Abdelali, Jérôme Lambert, Kheira Beldjord, Etienne Lengliné, Noémie De Gunzburg, Dominique Payet-Bornet, Ludovic Lhermitte, Hossein Mossafa,[...]. J Clin Oncol 2013
160
12

Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia.
Carmen Vicente, Claire Schwab, Michaël Broux, Ellen Geerdens, Sandrine Degryse, Sofie Demeyer, Idoya Lahortiga, Alannah Elliott, Lucy Chilton, Roberta La Starza,[...]. Haematologica 2015
108
12

The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.
Yu Liu, John Easton, Ying Shao, Jamie Maciaszek, Zhaoming Wang, Mark R Wilkinson, Kelly McCastlain, Michael Edmonson, Stanley B Pounds, Lei Shi,[...]. Nat Genet 2017
460
12

Further clinical delineation of the Börjeson-Forssman-Lehmann syndrome in patients with PHF6 mutations.
Melissa T Carter, David J Picketts, Alasdair G Hunter, Gail E Graham. Am J Med Genet A 2009
21
28

The Börjeson-Forssman-Lehman syndrome (BFLS, MIM #301900).
Jozef Gécz, Gillian Turner, John Nelson, Michael Partington. Eur J Hum Genet 2006
37
16

NOTCH1/FBXW7 mutation identifies a large subgroup with favorable outcome in adult T-cell acute lymphoblastic leukemia (T-ALL): a Group for Research on Adult Acute Lymphoblastic Leukemia (GRAALL) study.
Vahid Asnafi, Agnès Buzyn, Sandrine Le Noir, Frédéric Baleydier, Arnauld Simon, Kheira Beldjord, Oumedaly Reman, Francis Witz, Thierry Fagot, Emmanuelle Tavernier,[...]. Blood 2009
152
10

Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias.
Chen Shochat, Noa Tal, Obul R Bandapalli, Chiara Palmi, Ithamar Ganmore, Geertruy te Kronnie, Gunnar Cario, Giovanni Cazzaniga, Andreas E Kulozik, Martin Stanulla,[...]. J Exp Med 2011
244
10

A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study.
Monique L Den Boer, Marjon van Slegtenhorst, Renée X De Menezes, Meyling H Cheok, Jessica G C A M Buijs-Gladdines, Susan T C J M Peters, Laura J C M Van Zutven, H Berna Beverloo, Peter J Van der Spek, Gaby Escherich,[...]. Lancet Oncol 2009
602
10

Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults.
Paolo Gorello, Roberta La Starza, Emanuela Varasano, Sabina Chiaretti, Loredana Elia, Valentina Pierini, Gianluca Barba, Lucia Brandimarte, Barbara Crescenzi, Antonella Vitale,[...]. Haematologica 2010
32
18

Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations.
Martin Neumann, Sandra Heesch, Cornelia Schlee, Stefan Schwartz, Nicola Gökbuget, Dieter Hoelzer, Nikola P Konstandin, Bianka Ksienzyk, Sebastian Vosberg, Alexander Graf,[...]. Blood 2013
137
10

The molecular basis of T cell acute lymphoblastic leukemia.
Pieter Van Vlierberghe, Adolfo Ferrando. J Clin Invest 2012
330
10

Somatic mutations of PHF6 in patients with chronic myeloid leukemia in blast crisis.
Xianmin Li, Hong Yao, Zixing Chen, Qinrong Wang, Yun Zhao, Suning Chen. Leuk Lymphoma 2013
7
85

Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia.
Charles G Mullighan, Xiaoping Su, Jinghui Zhang, Ina Radtke, Letha A A Phillips, Christopher B Miller, Jing Ma, Wei Liu, Cheng Cheng, Brenda A Schulman,[...]. N Engl J Med 2009
939
10

TP53 mutations are frequent in adult acute lymphoblastic leukemia cases negative for recurrent fusion genes and correlate with poor response to induction therapy.
Sabina Chiaretti, Fulvia Brugnoletti, Simona Tavolaro, Silvia Bonina, Francesca Paoloni, Marilisa Marinelli, Nancy Patten, Massimiliano Bonifacio, Maria Grazia Kropp, Simona Sica,[...]. Haematologica 2013
44
13

Targetable kinase-activating lesions in Ph-like acute lymphoblastic leukemia.
Kathryn G Roberts, Yongjin Li, Debbie Payne-Turner, Richard C Harvey, Yung-Li Yang, Deqing Pei, Kelly McCastlain, Li Ding, Charles Lu, Guangchun Song,[...]. N Engl J Med 2014
861
10

Co-existence of PHF6 and NOTCH1 mutations in adult T-cell acute lymphoblastic leukemia.
Min Li, Lichan Xiao, Jingyan Xu, Run Zhang, Jingjing Guo, Justin Olson, Yujie Wu, Jianyong Li, Chunhua Song, Zheng Ge. Oncol Lett 2016
11
54

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.
Daniel A Arber, Attilio Orazi, Robert Hasserjian, Jürgen Thiele, Michael J Borowitz, Michelle M Le Beau, Clara D Bloomfield, Mario Cazzola, James W Vardiman. Blood 2016
10

Genomic and clinical characterization of B/T mixed phenotype acute leukemia reveals recurrent features and T-ALL like mutations.
Xiaoli Mi, Gabriel Griffin, Winston Lee, Sanjay Patel, Robert Ohgami, Chi Young Ok, Sa Wang, Julia T Geyer, Wenbin Xiao, Mikhail Roshal,[...]. Am J Hematol 2018
27
22

Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms.
T Mori, Y Nagata, H Makishima, M Sanada, Y Shiozawa, A Kon, T Yoshizato, A Sato-Otsubo, K Kataoka, Y Shiraishi,[...]. Leukemia 2016
25
24

The chromatin-binding protein Phf6 restricts the self-renewal of hematopoietic stem cells.
Satoru Miyagi, Patrycja Sroczynska, Yuko Kato, Yaeko Nakajima-Takagi, Motohiko Oshima, Ola Rizq, Naoya Takayama, Atsunori Saraya, Seiya Mizuno, Fumihiro Sugiyama,[...]. Blood 2019
20
30

PHF6 regulates hematopoietic stem and progenitor cells and its loss synergizes with expression of TLX3 to cause leukemia.
Helen M McRae, Alexandra L Garnham, Yifang Hu, Matthew T Witkowski, Mark A Corbett, Mathew P Dixon, Rose E May, Bilal N Sheikh, William Chiang, Andrew J Kueh,[...]. Blood 2019
24
25

Phf6-null hematopoietic stem cells have enhanced self-renewal capacity and oncogenic potentials.
Yueh-Chwen Hsu, Tsung-Chih Chen, Chien-Chin Lin, Chang-Tsu Yuan, Chia-Lang Hsu, Hsin-An Hou, Chein-Jun Kao, Po-Han Chuang, Yu-Ren Chen, Wen-Chien Chou,[...]. Blood Adv 2019
17
35


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.