A citation-based method for searching scientific literature

David H McDermott, Ji-Liang Gao, Qian Liu, Marie Siwicki, Craig Martens, Paejonette Jacobs, Daniel Velez, Erin Yim, Christine R Bryke, Nancy Hsu, Zunyan Dai, Martha M Marquesen, Elina Stregevsky, Nana Kwatemaa, Narda Theobald, Debra A Long Priel, Stefania Pittaluga, Mark A Raffeld, Katherine R Calvo, Irina Maric, Ronan Desmond, Kevin L Holmes, Douglas B Kuhns, Karl Balabanian, Françoise Bachelerie, Stephen F Porcella, Harry L Malech, Philip M Murphy. Cell 2015
Times Cited: 107







List of co-cited articles
1113 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease.
Paolo A Hernandez, Robert J Gorlin, John N Lukens, Shoichiro Taniuchi, Joze Bohinjec, Fleur Francois, Mary E Klotman, George A Diaz. Nat Genet 2003
436
34

Massive genomic rearrangement acquired in a single catastrophic event during cancer development.
Philip J Stephens, Chris D Greenman, Beiyuan Fu, Fengtang Yang, Graham R Bignell, Laura J Mudie, Erin D Pleasance, King Wai Lau, David Beare, Lucy A Stebbings,[...]. Cell 2011
28


Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline.
Wigard P Kloosterman, Victor Guryev, Mark van Roosmalen, Karen J Duran, Ewart de Bruijn, Saskia C M Bakker, Tom Letteboer, Bernadette van Nesselrooij, Ron Hochstenbach, Martin Poot,[...]. Hum Mol Genet 2011
204
23

Chromothripsis from DNA damage in micronuclei.
Cheng-Zhong Zhang, Alexander Spektor, Hauke Cornils, Joshua M Francis, Emily K Jackson, Shiwei Liu, Matthew Meyerson, David Pellman. Nature 2015
515
22

WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12.
Karl Balabanian, Bernard Lagane, José Luis Pablos, Lysiane Laurent, Thierry Planchenault, Olivier Verola, Celeste Lebbe, Delphine Kerob, Alain Dupuy, Olivier Hermine,[...]. Blood 2005
201
21

DNA breaks and chromosome pulverization from errors in mitosis.
Karen Crasta, Neil J Ganem, Regina Dagher, Alexandra B Lantermann, Elena V Ivanova, Yunfeng Pan, Luigi Nezi, Alexei Protopopov, Dipanjan Chowdhury, David Pellman. Nature 2012
703
21

A phase 1 clinical trial of long-term, low-dose treatment of WHIM syndrome with the CXCR4 antagonist plerixafor.
David H McDermott, Qian Liu, Daniel Velez, Lizbeeth Lopez, Sandra Anaya-O'Brien, Jean Ulrick, Nana Kwatemaa, Judy Starling, Thomas A Fleisher, Debra A Long Priel,[...]. Blood 2014
84
25

Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry.
Sarah Beaussant Cohen, Odile Fenneteau, Emmanuel Plouvier, Pierre-Simon Rohrlich, Gerard Daltroff, Isabelle Plantier, Alain Dupuy, Delphine Kerob, Blandine Beaupain, Pierre Bordigoni,[...]. Orphanet J Rare Dis 2012
63
31

Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.
Pengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, Shweta U Dhar, Katarzyna E Kołodziejska, Avinash V Dharmadhikari, M Lance Cooper, Joanna Wiszniewska, Feng Zhang, Marjorie A Withers,[...]. Cell 2011
282
18

Criteria for inference of chromothripsis in cancer genomes.
Jan O Korbel, Peter J Campbell. Cell 2013
292
18

The CXCR4 antagonist plerixafor corrects panleukopenia in patients with WHIM syndrome.
David H McDermott, Qian Liu, Jean Ulrick, Nana Kwatemaa, Sandra Anaya-O'Brien, Scott R Penzak, Joao Oliveira Filho, Debra A Long Priel, Corin Kelly, Mary Garofalo,[...]. Blood 2011
88
20

Proper desensitization of CXCR4 is required for lymphocyte development and peripheral compartmentalization in mice.
Karl Balabanian, Emilie Brotin, Vincent Biajoux, Laurence Bouchet-Delbos, Elodie Lainey, Odile Fenneteau, Dominique Bonnet, Laurence Fiette, Dominique Emilie, Françoise Bachelerie. Blood 2012
73
23

Impaired B-lymphopoiesis, myelopoiesis, and derailed cerebellar neuron migration in CXCR4- and SDF-1-deficient mice.
Q Ma, D Jones, P R Borghesani, R A Segal, T Nagasawa, T Kishimoto, R T Bronson, T A Springer. Proc Natl Acad Sci U S A 1998
17

CXCR4 is required for the quiescence of primitive hematopoietic cells.
Yuchun Nie, Yoon-Chi Han, Yong-Rui Zou. J Exp Med 2008
253
16


Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development.
Y R Zou, A H Kottmann, M Kuroda, I Taniuchi, D R Littman. Nature 1998
15

Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes.
Jan J Molenaar, Jan Koster, Danny A Zwijnenburg, Peter van Sluis, Linda J Valentijn, Ida van der Ploeg, Mohamed Hamdi, Johan van Nes, Bart A Westerman, Jennemiek van Arkel,[...]. Nature 2012
561
15

Defects of B-cell lymphopoiesis and bone-marrow myelopoiesis in mice lacking the CXC chemokine PBSF/SDF-1.
T Nagasawa, S Hirota, K Tachibana, N Takakura, S Nishikawa, Y Kitamura, N Yoshida, H Kikutani, T Kishimoto. Nature 1996
15

The CXCR4 antagonist plerixafor is a potential therapy for myelokathexis, WHIM syndrome.
David C Dale, Audrey Anna Bolyard, Merideth L Kelley, Ernest C Westrup, Vahagn Makaryan, Andrew Aprikyan, Brent Wood, Frank J Hsu. Blood 2011
63
23

Rapid mobilization of murine and human hematopoietic stem and progenitor cells with AMD3100, a CXCR4 antagonist.
Hal E Broxmeyer, Christie M Orschell, D Wade Clapp, Giao Hangoc, Scott Cooper, P Artur Plett, W Conrad Liles, Xiaxin Li, Barbara Graham-Evans, Timothy B Campbell,[...]. J Exp Med 2005
808
14

Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms.
Wigard P Kloosterman, Masoumeh Tavakoli-Yaraki, Markus J van Roosmalen, Ellen van Binsbergen, Ivo Renkens, Karen Duran, Lucia Ballarati, Sarah Vergult, Daniela Giardino, Kerstin Hansson,[...]. Cell Rep 2012
151
14

Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.
Tobias Rausch, David T W Jones, Marc Zapatka, Adrian M Stütz, Thomas Zichner, Joachim Weischenfeldt, Natalie Jäger, Marc Remke, David Shih, Paul A Northcott,[...]. Cell 2012
521
14

Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring.
Mirjam S de Pagter, Markus J van Roosmalen, Annette F Baas, Ivo Renkens, Karen J Duran, Ellen van Binsbergen, Masoumeh Tavakoli-Yaraki, Ron Hochstenbach, Lars T van der Veken, Edwin Cuppen,[...]. Am J Hum Genet 2015
47
27

CXCR2 and CXCR4 antagonistically regulate neutrophil trafficking from murine bone marrow.
Kyle J Eash, Adam M Greenbaum, Priya K Gopalan, Daniel C Link. J Clin Invest 2010
385
13

Chromothripsis: chromosomes in crisis.
Mathew J K Jones, Prasad V Jallepalli. Dev Cell 2012
96
13


WHIM syndrome: congenital immune deficiency disease.
Toshinao Kawai, Harry L Malech. Curr Opin Hematol 2009
120
13


A pivotal role for CXCL12 signaling in HPV-mediated transformation of keratinocytes: clues to understanding HPV-pathogenesis in WHIM syndrome.
Ken Y C Chow, Émilie Brotin, Youcef Ben Khalifa, Laetitia Carthagena, Sébastien Teissier, Anne Danckaert, Jean-Luc Galzi, Fernando Arenzana-Seisdedos, Françoise Thierry, Françoise Bachelerie. Cell Host Microbe 2010
48
25

CXCR4 dimerization and beta-arrestin-mediated signaling account for the enhanced chemotaxis to CXCL12 in WHIM syndrome.
Bernard Lagane, Ken Y C Chow, Karl Balabanian, Angélique Levoye, Julie Harriague, Thierry Planchenault, Françoise Baleux, Nathalie Gunera-Saad, Fernando Arenzana-Seisdedos, Françoise Bachelerie. Blood 2008
120
12

WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studies.
R J Gorlin, B Gelb, G A Diaz, K G Lofsness, M R Pittelkow, J R Fenyk. Am J Med Genet 2000
123
12

Successful umbilical cord blood stem cell transplantation in a child with WHIM syndrome.
Gergely Kriván, Melinda Erdos, Krisztián Kállay, Gábor Benyó, Agnes Tóth, János Sinkó, Vera Goda, Beáta Tóth, László Maródi. Eur J Haematol 2010
24
50


International Union of Basic and Clinical Pharmacology. [corrected]. LXXXIX. Update on the extended family of chemokine receptors and introducing a new nomenclature for atypical chemokine receptors.
Francoise Bachelerie, Adit Ben-Baruch, Amanda M Burkhardt, Christophe Combadiere, Joshua M Farber, Gerard J Graham, Richard Horuk, Alexander Hovard Sparre-Ulrich, Massimo Locati, Andrew D Luster,[...]. Pharmacol Rev 2013
477
11

Neutrophil mobilization via plerixafor-mediated CXCR4 inhibition arises from lung demargination and blockade of neutrophil homing to the bone marrow.
Sapna Devi, Yilin Wang, Weng Keong Chew, Ronald Lima, Noelia A-González, Citra N Z Mattar, Shu Zhen Chong, Andreas Schlitzer, Nadja Bakocevic, Samantha Chew,[...]. J Exp Med 2013
131
11

Punctuated evolution of prostate cancer genomes.
Sylvan C Baca, Davide Prandi, Michael S Lawrence, Juan Miguel Mosquera, Alessandro Romanel, Yotam Drier, Kyung Park, Naoki Kitabayashi, Theresa Y MacDonald, Mahmoud Ghandi,[...]. Cell 2013
721
11

Chromothripsis and Kataegis Induced by Telomere Crisis.
John Maciejowski, Yilong Li, Nazario Bosco, Peter J Campbell, Titia de Lange. Cell 2015
313
11

Endothelial and perivascular cells maintain haematopoietic stem cells.
Lei Ding, Thomas L Saunders, Grigori Enikolopov, Sean J Morrison. Nature 2012
11


The chemokine receptor CXCR4 is essential for vascularization of the gastrointestinal tract.
K Tachibana, S Hirota, H Iizasa, H Yoshida, K Kawabata, Y Kataoka, Y Kitamura, K Matsushima, N Yoshida, S Nishikawa,[...]. Nature 1998
10

Chromothripsis in congenital disorders and cancer: similarities and differences.
Wigard P Kloosterman, Edwin Cuppen. Curr Opin Cell Biol 2013
62
16

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration.
Colby Chiang, Jessie C Jacobsen, Carl Ernst, Carrie Hanscom, Adrian Heilbut, Ian Blumenthal, Ryan E Mills, Andrew Kirby, Amelia M Lindgren, Skye R Rudiger,[...]. Nat Genet 2012
169
10



Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients.
Laura Tassone, Daniele Moratto, William Vermi, Maria De Francesco, Lucia D Notarangelo, Fulvio Porta, Vassilios Lougaris, Fabio Facchetti, Alessandro Plebani, Raffaele Badolato. Blood 2010
41
24

A germline chromothripsis event stably segregating in 11 individuals through three generations.
Birgitte Bertelsen, Lusine Nazaryan-Petersen, Wei Sun, Mana M Mehrjouy, Gangcai Xie, Wei Chen, Lena E Hjermind, Peter E M Taschner, Zeynep Tümer. Genet Med 2016
36
27

Chromothripsis and cancer: causes and consequences of chromosome shattering.
Josep V Forment, Abderrahmane Kaidi, Stephen P Jackson. Nat Rev Cancer 2012
219
10

The essential functions of adipo-osteogenic progenitors as the hematopoietic stem and progenitor cell niche.
Yoshiki Omatsu, Tatsuki Sugiyama, Hiroshi Kohara, Gen Kondoh, Nobutaka Fujii, Kenji Kohno, Takashi Nagasawa. Immunity 2010
466
10

WHIM Syndrome Caused by Waldenström's Macroglobulinemia-Associated Mutation CXCR4 (L329fs).
Qian Liu, Catherina Pan, Lizbeeth Lopez, Jiliang Gao, Daniel Velez, Sandra Anaya-O'Brien, Jean Ulrick, Patricia Littel, John S Corns, Donald T Ellenburg,[...]. J Clin Immunol 2016
17
58


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.