A citation-based method for searching scientific literature

Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko, Vasileios Kargas, David Traynor, Ahmed Z Boukerrou, Norberto Escudero-Urquijo, Alexandre Faille, Alexis Bertrand, Maxim Rossmann, Beatriz Goyenechea, Li Jin, Jonathan Moreil, Olivier Alibeu, Blandine Beaupain, Christine Bôle-Feysot, Stefano Fumagalli, Sophie Kaltenbach, Jean-Alain Martignoles, Cécile Masson, Patrick Nitschké, Mélanie Parisot, Aurore Pouliet, Isabelle Radford-Weiss, Frédéric Tores, Jean-Pierre de Villartay, Mohammed Zarhrate, Ai Ling Koh, Kong Boo Phua, Bruno Reversade, Peter J Bond, Christine Bellanné-Chantelot, Isabelle Callebaut, François Delhommeau, Jean Donadieu, Alan J Warren, Patrick Revy. Nat Commun 2021
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Somatic genetic rescue in Mendelian haematopoietic diseases.
Patrick Revy, Caroline Kannengiesser, Alain Fischer. Nat Rev Genet 2019
31
50

Mutations in SBDS are associated with Shwachman-Diamond syndrome.
Graeme R B Boocock, Jodi A Morrison, Maja Popovic, Nicole Richards, Lynda Ellis, Peter R Durie, Johanna M Rommens. Nat Genet 2003
467
50

Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome.
Alyssa L Kennedy, Kasiani C Myers, James Bowman, Christopher J Gibson, Nicholas D Camarda, Elissa Furutani, Gwen M Muscato, Robert H Klein, Kaitlyn Ballotti, Shanshan Liu,[...]. Nat Commun 2021
12
50

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome.
Polina Stepensky, Montserrat Chacón-Flores, Katherine H Kim, Omar Abuzaitoun, Arnulfo Bautista-Santos, Natalia Simanovsky, Dritan Siliqi, Davide Altamura, Alfonso Méndez-Godoy, Abril Gijsbers,[...]. J Med Genet 2017
59
50


Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.
Jean Donadieu, Odile Fenneteau, Blandine Beaupain, Sandrine Beaufils, Florence Bellanger, Nizar Mahlaoui, Anne Lambilliotte, Nathalie Aladjidi, Yves Bertrand, Valérie Mialou,[...]. Haematologica 2012
69
33

Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.
Philip S Rosenberg, Cornelia Zeidler, Audrey A Bolyard, Blanche P Alter, Mary A Bonilla, Laurence A Boxer, Yigal Dror, Sally Kinsey, Daniel C Link, Peter E Newburger,[...]. Br J Haematol 2010
128
33

The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy.
Philip S Rosenberg, Blanche P Alter, Audrey A Bolyard, Mary Ann Bonilla, Laurence A Boxer, Bonnie Cham, Carol Fier, Melvin Freedman, George Kannourakis, Sally Kinsey,[...]. Blood 2006
269
33

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
Christoph Klein, Magda Grudzien, Giridharan Appaswamy, Manuela Germeshausen, Inga Sandrock, Alejandro A Schäffer, Chozhavendan Rathinam, Kaan Boztug, Beate Schwinzer, Nima Rezaei,[...]. Nat Genet 2007
312
33

Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis.
Julia Skokowa, Doris Steinemann, Jenny E Katsman-Kuipers, Cornelia Zeidler, Olga Klimenkova, Maksim Klimiankou, Murat Unalan, Siarhei Kandabarau, Vahagn Makaryan, Renee Beekman,[...]. Blood 2014
88
33

Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia.
Erika Van Nieuwenhove, John S Barber, Julika Neumann, Elien Smeets, Mathijs Willemsen, Emanuela Pasciuto, Teresa Prezzemolo, Vasiliki Lagou, Laura Seldeslachts, Bert Malengier-Devlies,[...]. J Allergy Clin Immunol 2020
11
33

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome.
Christine Bellanné-Chantelot, Barbara Schmaltz-Panneau, Caroline Marty, Odile Fenneteau, Isabelle Callebaut, Séverine Clauin, Aurélie Docet, Gandhi-Laurent Damaj, Thierry Leblanc, Isabelle Pellier,[...]. Blood 2018
46
33

Somatic mutations and clonal hematopoiesis in congenital neutropenia.
Jun Xia, Christopher A Miller, Jack Baty, Amrita Ramesh, Matthew R M Jotte, Robert S Fulton, Tiphanie P Vogel, Megan A Cooper, Kelly J Walkovich, Vahagn Makaryan,[...]. Blood 2018
54
33

Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis.
Barbara Pressato, Roberto Valli, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Br J Haematol 2012
34
33

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.
Raphael Carapito, Martina Konantz, Catherine Paillard, Zhichao Miao, Angélique Pichot, Magalie S Leduc, Yaping Yang, Katie L Bergstrom, Donald H Mahoney, Deborah L Shardy,[...]. J Clin Invest 2017
70
33

Interleukin-12 and Interleukin-23 Blockade in Leukocyte Adhesion Deficiency Type 1.
Niki M Moutsopoulos, Christa S Zerbe, Teresa Wild, Nicolas Dutzan, Laurie Brenchley, Giovanni DiPasquale, Gulbu Uzel, Karen C Axelrod, Andrea Lisco, Lucia D Notarangelo,[...]. N Engl J Med 2017
67
16


SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation.
Ottavia M Delmonte, Jenna R E Bergerson, Tomoki Kawai, Hye Sun Kuehn, David H McDermott, Irene Cortese, Michael T Zimmermann, A Kerry Dobbs, Marita Bosticardo, Danielle Fink,[...]. Blood 2021
5
20


The spectrum of ELANE mutations and their implications in severe congenital and cyclic neutropenia.
Manuela Germeshausen, Sabine Deerberg, Yvonne Peter, Christina Reimer, Christian P Kratz, Matthias Ballmaier. Hum Mutat 2013
47
16

A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome.
Simone Cesaro, Anna Pegoraro, Laura Sainati, Vincenzina Lucidi, Enza Montemitro, Paola Corti, Ugo Ramenghi, Cristina Nasi, Giuseppe Menna, Marco Zecca,[...]. J Pediatr 2020
2
50

Quality of life and patient-reported outcomes in chronic severe neutropenia conditions.
Thomas F Michniacki, Lauren E Merz, Harlan McCaffery, James A Connelly, Kelly Walkovich. Int J Hematol 2021
1
100

Haematopoietic and immune defects associated with GATA2 mutation.
Matthew Collin, Rachel Dickinson, Venetia Bigley. Br J Haematol 2015
128
16


TP53 mutations: the dawn of Shwachman clones.
Jean Donadieu, François Delhommeau. Blood 2018
6
16

Therapeutic targeting of cathepsin C: from pathophysiology to treatment.
Brice Korkmaz, George H Caughey, Iain Chapple, Francis Gauthier, Josefine Hirschfeld, Dieter E Jenne, Ralph Kettritz, Gilles Lalmanach, Anne-Sophie Lamort, Conni Lauritzen,[...]. Pharmacol Ther 2018
45
16

The phenotype of human STK4 deficiency.
Hengameh Abdollahpour, Giridharan Appaswamy, Daniel Kotlarz, Jana Diestelhorst, Rita Beier, Alejandro A Schäffer, E Michael Gertz, Axel Schambach, Hans H Kreipe, Dietmar Pfeifer,[...]. Blood 2012
194
16

Survival and differentiation defects contribute to neutropenia in glucose-6-phosphatase-β (G6PC3) deficiency in a model of mouse neutrophil granulocyte differentiation.
S Gautam, S Kirschnek, I E Gentle, C Kopiniok, P Henneke, H Häcker, L Malleret, A Belaaouaj, G Häcker. Cell Death Differ 2013
14
16

Prevalence of neutropenia in the U.S. population: age, sex, smoking status, and ethnic differences.
Matthew M Hsieh, James E Everhart, Danita D Byrd-Holt, John F Tisdale, Griffin P Rodgers. Ann Intern Med 2007
209
16

Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene.
Ludovica Volpi, Gaia Roversi, Elisa Adele Colombo, Nico Leijsten, Daniela Concolino, Andrea Calabria, Maria Antonietta Mencarelli, Michele Fimiani, Fabio Macciardi, Rolph Pfundt,[...]. Am J Hum Genet 2010
103
16

TCIRG1-associated congenital neutropenia.
Vahagn Makaryan, Elisabeth A Rosenthal, Audrey Anna Bolyard, Merideth L Kelley, Jennifer E Below, Michael J Bamshad, Kathryn M Bofferding, Joshua D Smith, Kati Buckingham, Laurence A Boxer,[...]. Hum Mutat 2014
24
16


Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis.
M Horwitz, K F Benson, R E Person, A G Aprikyan, D C Dale. Nat Genet 1999
303
16

Leucocyte adhesion deficiency-A multicentre national experience.
Baruch Wolach, Ronit Gavrieli, Ofir Wolach, Tal Stauber, Omar Abuzaitoun, Amir Kuperman, Yaakov Amir, Polina Stepensky, Raz Somech, Amos Etzioni. Eur J Clin Invest 2019
20
16

CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder.
Saskia B Wortmann, Szymon Ziętkiewicz, Maria Kousi, Radek Szklarczyk, Tobias B Haack, Søren W Gersting, Ania C Muntau, Aleksandar Rakovic, G Herma Renkema, Richard J Rodenburg,[...]. Am J Hum Genet 2015
54
16

CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduria.
Carol Saunders, Laurie Smith, Flemming Wibrand, Kirstine Ravn, Peter Bross, Isabelle Thiffault, Mette Christensen, Andrea Atherton, Emily Farrow, Neil Miller,[...]. Am J Hum Genet 2015
30
16

Neonatal neutropenia. Clinical manifestations, cause, and outcome.
J E Baley, E K Stork, P I Warkentin, S B Shurin. Am J Dis Child 1988
53
16


Diagnosis of Papillon-Lefèvre syndrome: review of the literature and a case report.
Zygmunt Adamski, Dorota Burchardt, Tamara Pawlaczyk-Kamieńska, Maria Borysewicz-Lewicka, Marzena Wyganowska-Świątkowska. Postepy Dermatol Alergol 2020
5
20

When non-Whiteness becomes a condition.
Lauren E Merz, Maureen Achebe. Blood 2021
8
16


High incidence of significant bone loss in patients with severe congenital neutropenia (Kostmann's syndrome).
E Yakisan, E Schirg, C Zeidler, N J Bishop, A Reiter, A Hirt, H Riehm, K Welte. J Pediatr 1997
47
16

Plerixafor for the Treatment of WHIM Syndrome.
David H McDermott, Diana V Pastrana, Katherine R Calvo, Stefania Pittaluga, Daniel Velez, Elena Cho, Qian Liu, Hugh H Trout, João F Neves, Pamela J Gardner,[...]. N Engl J Med 2019
38
16

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome.
M Delépine, M Nicolino, T Barrett, M Golamaully, G M Lathrop, C Julier. Nat Genet 2000
568
16

Neutrophil count in African Americans: lowering the target cutoff to initiate or resume chemotherapy?
Matthew M Hsieh, John F Tisdale, Griffin P Rodgers, Neal S Young, Edward L Trimble, Richard F Little. J Clin Oncol 2010
41
16

Admixture mapping of white cell count: genetic locus responsible for lower white blood cell count in the Health ABC and Jackson Heart studies.
Michael A Nalls, James G Wilson, Nick J Patterson, Arti Tandon, Joseph M Zmuda, Scott Huntsman, Melissa Garcia, Donglei Hu, Rongling Li, Brock A Beamer,[...]. Am J Hum Genet 2008
127
16

Post-COVID-19 severe neutropenia.
Boutheina Bouslama, Clément Pierret, Fatima Khelfaoui, Christine Bellanné-Chantelot, Jean Donadieu, Sébastien Héritier. Pediatr Blood Cancer 2021
5
20

Autoimmune neutropenia associated with chronic active hepatitis.
L A Boxer, M Yokoyama, R A Wiebe. Am J Med 1972
19
16

Results of a phase 2 trial of an oral CXCR4 antagonist, mavorixafor, for treatment of WHIM syndrome.
David C Dale, Frank Firkin, Audrey Anna Bolyard, Merideth Kelley, Vahagn Makaryan, Kenneth J Gorelick, Tarek Ebrahim, Varun Garg, Weihua Tang, Honghua Jiang,[...]. Blood 2020
8
16

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060).
P G Barth, R J Wanders, P Vreken, E A Janssen, J Lam, F Baas. J Inherit Metab Dis 1999
95
16


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.