A citation-based method for searching scientific literature

Simon Stritt, Paquita Nurden, Ernest Turro, Daniel Greene, Sjoert B Jansen, Sarah K Westbury, Romina Petersen, William J Astle, Sandrine Marlin, Tadbir K Bariana, Myrto Kostadima, Claire Lentaigne, Stephanie Maiwald, Sofia Papadia, Anne M Kelly, Jonathan C Stephens, Christopher J Penkett, Sofie Ashford, Salih Tuna, Steve Austin, Tamam Bakchoul, Peter Collins, Rémi Favier, Michele P Lambert, Mary Mathias, Carolyn M Millar, Rutendo Mapeta, David J Perry, Sol Schulman, Ilenia Simeoni, Chantal Thys, Keith Gomez, Wendy N Erber, Kathleen Stirrups, Augusto Rendon, John R Bradley, Chris van Geet, F Lucy Raymond, Michael A Laffan, Alan T Nurden, Bernhard Nieswandt, Sylvia Richardson, Kathleen Freson, Willem H Ouwehand, Andrew D Mumford. Blood 2016
Times Cited: 75







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



Times Cited
  Times     Co-cited
Similarity


A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.
Ernest Turro, Daniel Greene, Anouck Wijgaerts, Chantal Thys, Claire Lentaigne, Tadbir K Bariana, Sarah K Westbury, Anne M Kelly, Dominik Selleslag, Jonathan C Stephens,[...]. Sci Transl Med 2016
53
47

ACTN1 mutations cause congenital macrothrombocytopenia.
Shinji Kunishima, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Masashi Sanada, Hideki Muramatsu, Kenichi Chiba, Hiroko Tanaka, Koji Miyazaki, Michio Sakai,[...]. Am J Hum Genet 2013
128
32

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.
Ilenia Simeoni, Jonathan C Stephens, Fengyuan Hu, Sri V V Deevi, Karyn Megy, Tadbir K Bariana, Claire Lentaigne, Sol Schulman, Suthesh Sivapalaratnam, Minka J A Vries,[...]. Blood 2016
110
28

Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome.
Paquita Nurden, Najet Debili, Isabelle Coupry, Marijke Bryckaert, Ibtissam Youlyouz-Marfak, Guilhem Solé, Anne-Cécile Pons, Eliane Berrou, Frédéric Adam, Alexandre Kauskot,[...]. Blood 2011
100
25

Inherited platelet disorders: toward DNA-based diagnosis.
Claire Lentaigne, Kathleen Freson, Michael A Laffan, Ernest Turro, Willem H Ouwehand. Blood 2016
79
25

The formin DIAPH1 (mDia1) regulates megakaryocyte proplatelet formation by remodeling the actin and microtubule cytoskeletons.
Jiajia Pan, Larissa Lordier, Deborah Meyran, Philippe Rameau, Yann Lecluse, Susan Kitchen-Goosen, Idinath Badirou, Hayat Mokrani, Shuh Narumiya, Arthur S Alberts,[...]. Blood 2014
45
42

Mutation of the beta1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly.
Shinji Kunishima, Ryoji Kobayashi, Tomohiko J Itoh, Motohiro Hamaguchi, Hidehiko Saito. Blood 2009
99
22

Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
Irina Pleines, Joanne Woods, Stephane Chappaz, Verity Kew, Nicola Foad, José Ballester-Beltrán, Katja Aurbach, Chiara Lincetto, Rachael M Lane, Galina Schevzov,[...]. J Clin Invest 2017
31
54

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.
Sarah K Westbury, Ernest Turro, Daniel Greene, Claire Lentaigne, Anne M Kelly, Tadbir K Bariana, Ilenia Simeoni, Xavier Pillois, Antony Attwood, Steve Austin,[...]. Genome Med 2015
79
21

MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.
Alessandro Pecci, Catherine Klersy, Paolo Gresele, Kieran J D Lee, Daniela De Rocco, Valeria Bozzi, Giovanna Russo, Paula G Heller, Giuseppe Loffredo, Matthias Ballmaier,[...]. Hum Mutat 2014
106
21

Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.
Leila Noetzli, Richard W Lo, Alisa B Lee-Sherick, Michael Callaghan, Patrizia Noris, Anna Savoia, Madhvi Rajpurkar, Kenneth Jones, Katherine Gowan, Carlo Balduini,[...]. Nat Genet 2015
153
20

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Cornelis A Albers, Dirk S Paul, Harald Schulze, Kathleen Freson, Jonathan C Stephens, Peter A Smethurst, Jennifer D Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone,[...]. Nat Genet 2012
251
20

Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1).
C Neuhaus, R Lang-Roth, U Zimmermann, R Heller, T Eisenberger, M Weikert, S Markus, M Knipper, H J Bolz. Clin Genet 2017
26
57

Spectrum of the mutations in Bernard-Soulier syndrome.
Anna Savoia, Shinji Kunishima, Daniela De Rocco, Barbara Zieger, Margaret L Rand, Nuria Pujol-Moix, Umran Caliskan, Huseyin Tokgoz, Alessandro Pecci, Patrizia Noris,[...]. Hum Mutat 2014
71
19

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.
Patrizia Noris, Silverio Perrotta, Marco Seri, Alessandro Pecci, Chiara Gnan, Giuseppe Loffredo, Nuria Pujol-Moix, Marco Zecca, Francesca Scognamiglio, Daniela De Rocco,[...]. Blood 2011
157
18

A dominant-negative GFI1B mutation in the gray platelet syndrome.
Davide Monteferrario, Nikhita A Bolar, Anna E Marneth, Konnie M Hebeda, Saskia M Bergevoet, Hans Veenstra, Britta A P Laros-van Gorkom, Marius A MacKenzie, Cyrus Khandanpour, Lacramiora Botezatu,[...]. N Engl J Med 2014
97
18

Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.
Walter H A Kahr, Fred G Pluthero, Abdul Elkadri, Neil Warner, Marko Drobac, Chang Hua Chen, Richard W Lo, Ling Li, Ren Li, Qi Li,[...]. Nat Commun 2017
95
18

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.
Sarah J Fletcher, Ben Johnson, Gillian C Lowe, Danai Bem, Sian Drake, Marie Lordkipanidzé, Isabel Sánchez Guiú, Ban Dawood, José Rivera, Michael A Simpson,[...]. J Clin Invest 2015
41
31

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects.
Ben Johnson, Gillian C Lowe, Jane Futterer, Marie Lordkipanidzé, David MacDonald, Michael A Simpson, Isabel Sanchez-Guiú, Sian Drake, Danai Bem, Vincenzo Leo,[...]. Haematologica 2016
70
18

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
17

Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.
Tetsuya Niihori, Meri Ouchi-Uchiyama, Yoji Sasahara, Takashi Kaneko, Yoshiko Hashii, Masahiro Irie, Atsushi Sato, Yuka Saito-Nanjo, Ryo Funayama, Takeshi Nagashima,[...]. Am J Hum Genet 2015
38
31

ADF/n-cofilin-dependent actin turnover determines platelet formation and sizing.
Markus Bender, Anita Eckly, John H Hartwig, Margitta Elvers, Irina Pleines, Shuchi Gupta, Georg Krohne, Elisabeth Jeanclos, Antje Gohla, Christine Gurniak,[...]. Blood 2010
55
21


Microtubule sliding drives proplatelet elongation and is dependent on cytoplasmic dynein.
Markus Bender, Jonathan N Thon, Allen J Ehrlicher, Stephen Wu, Linas Mazutis, Emoke Deschmann, Martha Sola-Visner, Joseph E Italiano, John H Hartwig. Blood 2015
54
22

Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders.
José M Bastida, María L Lozano, Rocío Benito, Kamila Janusz, Verónica Palma-Barqueros, Mónica Del Rey, Jesús M Hernández-Sánchez, Susana Riesco, Nuria Bermejo, Hermenegildo González-García,[...]. Haematologica 2018
58
20

Phenotype description and response to thrombopoietin receptor agonist in DIAPH1-related disorder.
Sarah K Westbury, Kate Downes, Claire Burney, Maria L Lozano, Samya G Obaji, Cheng Hock Toh, Teresa Sevivas, Neil V Morgan, Wendy N Erber, Carly Kempster,[...]. Blood Adv 2018
18
66


A new form of macrothrombocytopenia induced by a germ-line mutation in the PRKACG gene.
Vladimir T Manchev, Morgane Hilpert, Eliane Berrou, Ziane Elaib, Achille Aouba, Siham Boukour, Sylvie Souquere, Gerard Pierron, Philippe Rameau, Robert Andrews,[...]. Blood 2014
40
27

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.
E D Lynch, M K Lee, J E Morrow, P L Welcsh, P E León, M C King. Science 1997
278
13

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome.
Walter H A Kahr, Jesse Hinckley, Ling Li, Hansjörg Schwertz, Hilary Christensen, Jesse W Rowley, Fred G Pluthero, Denisa Urban, Shay Fabbro, Brie Nixon,[...]. Nat Genet 2011
150
13

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.
Patrizia Noris, Ginevra Biino, Alessandro Pecci, Elisa Civaschi, Anna Savoia, Marco Seri, Federica Melazzini, Giuseppe Loffredo, Giovanna Russo, Valeria Bozzi,[...]. Blood 2014
67
14

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.
Alessandro Pecci, Paolo Gresele, Catherine Klersy, Anna Savoia, Patrizia Noris, Tiziana Fierro, Valeria Bozzi, Anna Maria Mezzasoma, Federica Melazzini, Carlo L Balduini. Blood 2010
100
13

Cytoskeletal perturbation leads to platelet dysfunction and thrombocytopenia in variant forms of Glanzmann thrombasthenia.
Loredana Bury, Emanuela Falcinelli, Davide Chiasserini, Timothy A Springer, Joseph E Italiano, Paolo Gresele. Haematologica 2016
32
31

Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small-platelet thrombocytopenia.
C Levin, A Koren, E Pretorius, N Rosenberg, B Shenkman, H Hauschner, L Zalman, M Khayat, I Salama, O Elpeleg,[...]. J Thromb Haemost 2015
27
37

Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1.
William S Stevenson, David J Rabbolini, Lucinda Beutler, Qiang Chen, Sara Gabrielli, Joel P Mackay, Timothy A Brighton, Christopher M Ward, Marie-Christine Morel-Kopp. Blood 2015
38
26


Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect.
Markus Bender, Simon Stritt, Paquita Nurden, Judith M M van Eeuwijk, Barbara Zieger, Karim Kentouche, Harald Schulze, Henner Morbach, David Stegner, Katrin G Heinze,[...]. Nat Commun 2014
54
18

The incredible journey: From megakaryocyte development to platelet formation.
Kellie R Machlus, Joseph E Italiano. J Cell Biol 2013
308
13

Progressive macrothrombocytopenia and hearing loss in a large family with DIAPH1 related disease.
Akira Ganaha, Tadashi Kaname, Ayano Shinjou, Yasutsugu Chinen, Kumiko Yanagi, Teruyuki Higa, Shunsuke Kondo, Mikio Suzuki. Am J Med Genet A 2017
11
90

Formin proteins in megakaryocytes and platelets: regulation of actin and microtubule dynamics.
Malou Zuidscherwoude, Hannah L H Green, Steven G Thomas. Platelets 2019
16
62

Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation.
Dominique Bluteau, Alessandra Balduini, Nathalie Balayn, Manuela Currao, Paquita Nurden, Caroline Deswarte, Guy Leverger, Patrizia Noris, Silverio Perrotta, Eric Solary,[...]. J Clin Invest 2014
97
12

Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders.
V C Leo, N V Morgan, D Bem, M L Jones, G C Lowe, M Lordkipanidzé, S Drake, M A Simpson, P Gissen, A Mumford,[...]. J Thromb Haemost 2015
41
21

Defects in TRPM7 channel function deregulate thrombopoiesis through altered cellular Mg(2+) homeostasis and cytoskeletal architecture.
Simon Stritt, Paquita Nurden, Remi Favier, Marie Favier, Silvia Ferioli, Sanjeev K Gotru, Judith M M van Eeuwijk, Harald Schulze, Alan T Nurden, Michele P Lambert,[...]. Nat Commun 2016
52
17

Deficiency in the Wiskott-Aldrich protein induces premature proplatelet formation and platelet production in the bone marrow compartment.
Siham Sabri, Adlen Foudi, Siham Boukour, Brigitte Franc, Sabine Charrier, Martine Jandrot-Perrus, Richard W Farndale, Abdelali Jalil, Mike P Blundell, Elisabeth M Cramer,[...]. Blood 2006
136
12

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
William J Astle, Heather Elding, Tao Jiang, Dave Allen, Dace Ruklisa, Alice L Mann, Daniel Mead, Heleen Bouman, Fernando Riveros-Mckay, Myrto A Kostadima,[...]. Cell 2016
429
12

Cdc42-dependent F-actin dynamics drive structuration of the demarcation membrane system in megakaryocytes.
A Antkowiak, J Viaud, S Severin, M Zanoun, L Ceccato, G Chicanne, C Strassel, A Eckly, C Leon, C Gachet,[...]. J Thromb Haemost 2016
22
40

Multiple alterations of platelet functions dominated by increased secretion in mice lacking Cdc42 in platelets.
Irina Pleines, Anita Eckly, Margitta Elvers, Ina Hagedorn, Sandra Eliautou, Markus Bender, Xunwei Wu, Francois Lanza, Christian Gachet, Cord Brakebusch,[...]. Blood 2010
89
12

Deletion of the Arp2/3 complex in megakaryocytes leads to microthrombocytopenia in mice.
David S Paul, Caterina Casari, Congying Wu, Raymond Piatt, Swetha Pasala, Robert A Campbell, Kathryn O Poe, Dorsaf Ghalloussi, Robert H Lee, Jeremy D Rotty,[...]. Blood Adv 2017
18
50

Defective tubulin organization and proplatelet formation in murine megakaryocytes lacking Rac1 and Cdc42.
Irina Pleines, Sebastian Dütting, Deya Cherpokova, Anita Eckly, Imke Meyer, Martina Morowski, Georg Krohne, Harald Schulze, Christian Gachet, Najet Debili,[...]. Blood 2013
69
13

ANKRD26-related thrombocytopenia and myeloid malignancies.
Patrizia Noris, Remi Favier, Marie-Christine Alessi, Amy E Geddis, Shinji Kunishima, Paula G Heller, Paola Giordano, Karen Y Niederhoffer, James B Bussel, Gian Marco Podda,[...]. Blood 2013
91
10


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.