A citation-based method for searching scientific literature

Laura E Egolf, Zalman Vaksman, Gonzalo Lopez, Jo Lynne Rokita, Apexa Modi, Patricia V Basta, Hakon Hakonarson, Andrew F Olshan, Sharon J Diskin. Am J Hum Genet 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


The genetic landscape of high-risk neuroblastoma.
Trevor J Pugh, Olena Morozova, Edward F Attiyeh, Shahab Asgharzadeh, Jun S Wei, Daniel Auclair, Scott L Carter, Kristian Cibulskis, Megan Hanna, Adam Kiezun,[...]. Nat Genet 2013
607
36

Germline Mutations in Predisposition Genes in Pediatric Cancer.
Jinghui Zhang, Michael F Walsh, Gang Wu, Michael N Edmonson, Tanja A Gruber, John Easton, Dale Hedges, Xiaotu Ma, Xin Zhou, Donald A Yergeau,[...]. N Engl J Med 2015
494
27

The landscape of genomic alterations across childhood cancers.
Susanne N Gröbner, Barbara C Worst, Joachim Weischenfeldt, Ivo Buchhalter, Kortine Kleinheinz, Vasilisa A Rudneva, Pascal D Johann, Gnana Prakash Balasubramanian, Maia Segura-Wang, Sebastian Brabetz,[...]. Nature 2018
436
27

Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism.
Derek A Oldridge, Andrew C Wood, Nina Weichert-Leahey, Ian Crimmins, Robyn Sussman, Cynthia Winter, Lee D McDaniel, Maura Diamond, Lori S Hart, Shizhen Zhu,[...]. Nature 2015
164
27

Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma.
Isabelle Janoueix-Lerosey, Delphine Lequin, Laurence Brugières, Agnès Ribeiro, Loïc de Pontual, Valérie Combaret, Virginie Raynal, Alain Puisieux, Gudrun Schleiermacher, Gaëlle Pierron,[...]. Nature 2008
573
27

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
D Williams Parsons, Angshumoy Roy, Yaping Yang, Tao Wang, Sarah Scollon, Katie Bergstrom, Robin A Kerstein, Stephanie Gutierrez, Andrea K Petersen, Abhishek Bavle,[...]. JAMA Oncol 2016
217
27

Identification of ALK as a major familial neuroblastoma predisposition gene.
Yaël P Mossé, Marci Laudenslager, Luca Longo, Kristina A Cole, Andrew Wood, Edward F Attiyeh, Michael J Laquaglia, Rachel Sennett, Jill E Lynch, Patrizia Perri,[...]. Nature 2008
804
27

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
R G Walters, S Jacquemont, A Valsesia, A J de Smith, D Martinet, J Andersson, M Falchi, F Chen, J Andrieux, S Lobbens,[...]. Nature 2010
317
27

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
27

PHOX2B mutations and genetic predisposition to neuroblastoma.
Patrizia Perri, Tiziana Bachetti, Luca Longo, Ivana Matera, Marco Seri, Gian Paolo Tonini, Isabella Ceccherini. Oncogene 2005
33
18

Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor.
Flora Cimmino, Marianna Avitabile, Sharon J Diskin, Zalman Vaksman, Piero Pignataro, Daniela Formicola, Antonella Cardinale, Alessandro Testori, Jan Koster, Carmen de Torres,[...]. Int J Cancer 2018
31
18

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.
Mario Capasso, Marcella Devoto, Cuiping Hou, Shahab Asgharzadeh, Joseph T Glessner, Edward F Attiyeh, Yael P Mosse, Cecilia Kim, Sharon J Diskin, Kristina A Cole,[...]. Nat Genet 2009
214
18

The Phox2B homeobox gene is mutated in sporadic neuroblastomas.
Vera van Limpt, Alexander Schramm, Arjan van Lakeman, Peter Sluis, Alvin Chan, Max van Noesel, Frank Baas, Huib Caron, Angelika Eggert, Rogier Versteeg. Oncogene 2004
87
18

Relative frequency and morphology of cancers in carriers of germline TP53 mutations.
J M Birch, R D Alston, R J McNally, D G Evans, A M Kelsey, M Harris, O B Eden, J M Varley. Oncogene 2001
293
18

Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups.
Saskia M Maas, Fleur Vansenne, Daniel J M Kadouch, Abdulla Ibrahim, Jet Bliek, Saskia Hopman, Marcel M Mannens, Johannes H M Merks, Eamonn R Maher, Raoul C Hennekam. Am J Med Genet A 2016
89
18

CASC15-S Is a Tumor Suppressor lncRNA at the 6p22 Neuroblastoma Susceptibility Locus.
Mike R Russell, Annalise Penikis, Derek A Oldridge, Juan R Alvarez-Dominguez, Lee McDaniel, Maura Diamond, Olivia Padovan, Pichai Raman, Yimei Li, Jun S Wei,[...]. Cancer Res 2015
96
18

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.
John M Maris, Yael P Mosse, Jonathan P Bradfield, Cuiping Hou, Stefano Monni, Richard H Scott, Shahab Asgharzadeh, Edward F Attiyeh, Sharon J Diskin, Marci Laudenslager,[...]. N Engl J Med 2008
201
18

Causative and common PHOX2B variants define a broad phenotypic spectrum.
Tiziana Bachetti, Isabella Ceccherini. Clin Genet 2020
14
18

ALK mutations confer differential oncogenic activation and sensitivity to ALK inhibition therapy in neuroblastoma.
Scott C Bresler, Daniel A Weiser, Peter J Huwe, Jin H Park, Kateryna Krytska, Hannah Ryles, Marci Laudenslager, Eric F Rappaport, Andrew C Wood, Patrick W McGrady,[...]. Cancer Cell 2014
189
18

The risk-associated long noncoding RNA NBAT-1 controls neuroblastoma progression by regulating cell proliferation and neuronal differentiation.
Gaurav Kumar Pandey, Sanhita Mitra, Santhilal Subhash, Falk Hertwig, Meena Kanduri, Kankadeb Mishra, Susanne Fransson, Abiarchana Ganeshram, Tanmoy Mondal, Sashidhar Bandaru,[...]. Cancer Cell 2014
222
18


Chromosome 1p and 11q deletions and outcome in neuroblastoma.
Edward F Attiyeh, Wendy B London, Yael P Mossé, Qun Wang, Cynthia Winter, Deepa Khazi, Patrick W McGrady, Robert C Seeger, A Thomas Look, Hiroyuki Shimada,[...]. N Engl J Med 2005
349
18

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.
Jeanne Amiel, Béatrice Laudier, Tania Attié-Bitach, Ha Trang, Loïc de Pontual, Blanca Gener, Delphine Trochet, Heather Etchevers, Pierre Ray, Michel Simonneau,[...]. Nat Genet 2003
550
18

Oncogenic mutations of ALK kinase in neuroblastoma.
Yuyan Chen, Junko Takita, Young Lim Choi, Motohiro Kato, Miki Ohira, Masashi Sanada, Lili Wang, Manabu Soda, Akira Kikuchi, Takashi Igarashi,[...]. Nature 2008
594
18

Rare variants in TP53 and susceptibility to neuroblastoma.
Sharon J Diskin, Mario Capasso, Maura Diamond, Derek A Oldridge, Karina Conkrite, Kristopher R Bosse, Mike R Russell, Achille Iolascon, Hakon Hakonarson, Marcella Devoto,[...]. J Natl Cancer Inst 2014
76
18

Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci.
Le B Nguyen, Sharon J Diskin, Mario Capasso, Kai Wang, Maura A Diamond, Joseph Glessner, Cecilia Kim, Edward F Attiyeh, Yael P Mosse, Kristina Cole,[...]. PLoS Genet 2011
117
18


Neuroblastoma-A Neural Crest Derived Embryonal Malignancy.
John Inge Johnsen, Cecilia Dyberg, Malin Wickström. Front Mol Neurosci 2019
45
18

Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility.
Mario Capasso, Sharon J Diskin, Francesca Totaro, Luca Longo, Marilena De Mariano, Roberta Russo, Flora Cimmino, Hakon Hakonarson, Gian Paolo Tonini, Marcella Devoto,[...]. Carcinogenesis 2013
76
18

LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppression.
Jan J Molenaar, Raquel Domingo-Fernández, Marli E Ebus, Sven Lindner, Jan Koster, Ksenija Drabek, Pieter Mestdagh, Peter van Sluis, Linda J Valentijn, Johan van Nes,[...]. Nat Genet 2012
241
18

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.
Xiao Chang, Yan Zhao, Cuiping Hou, Joseph Glessner, Lee McDaniel, Maura A Diamond, Kelly Thomas, Jin Li, Zhi Wei, Yichuan Liu,[...]. Nat Commun 2017
19
18

Dualistic Role of BARD1 in Cancer.
Flora Cimmino, Daniela Formicola, Mario Capasso. Genes (Basel) 2017
29
18

Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.
Eric R Gamazon, Navin Pinto, Anuar Konkashbaev, Hae Kyung Im, Sharon J Diskin, Wendy B London, John M Maris, M Eileen Dolan, Nancy J Cox, Susan L Cohn. J Natl Cancer Inst 2013
26
18

Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.
Katrina Tatton-Brown, Anne Murray, Sandra Hanks, Jenny Douglas, Ruth Armstrong, Siddharth Banka, Lynne M Bird, Carol L Clericuzio, Valerie Cormier-Daire, Tom Cushing,[...]. Am J Med Genet A 2013
73
18

Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma.
Lee D McDaniel, Karina L Conkrite, Xiao Chang, Mario Capasso, Zalman Vaksman, Derek A Oldridge, Anna Zachariou, Millicent Horn, Maura Diamond, Cuiping Hou,[...]. PLoS Genet 2017
35
18

Multiple mechanisms disrupt the let-7 microRNA family in neuroblastoma.
John T Powers, Kaloyan M Tsanov, Daniel S Pearson, Frederik Roels, Catherine S Spina, Richard Ebright, Marc Seligson, Yvanka de Soysa, Patrick Cahan, Jessica Theißen,[...]. Nature 2016
110
18

Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30-year-old mystery.
R Neil Schimke, Debra L Collins, Catherine A Stolle. Am J Med Genet A 2010
60
18

Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene.
Marianna Avitabile, Mariangela Succoio, Alessandro Testori, Antonella Cardinale, Zalman Vaksman, Vito Alessandro Lasorsa, Sueva Cantalupo, Matteo Esposito, Flora Cimmino, Annalaura Montella,[...]. Carcinogenesis 2020
7
28

The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma.
Mario Capasso, Lee D McDaniel, Flora Cimmino, Andrea Cirino, Daniela Formicola, Mike R Russell, Pichai Raman, Kristina A Cole, Sharon J Diskin. J Cell Mol Med 2017
40
18

Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.
John M Maris, Matthew J Weiss, Yael Mosse, George Hii, Chun Guo, Peter S White, Michael D Hogarty, Tamar Mirensky, Garrett M Brodeur, Timothy R Rebbeck,[...]. Cancer Res 2002
56
18

Identification of GALNT14 as a novel neuroblastoma predisposition gene.
Marilena De Mariano, Roberta Gallesio, Marco Chierici, Cesare Furlanello, Massimo Conte, Alberto Garaventa, Michela Croce, Silvano Ferrini, Gian Paolo Tonini, Luca Longo. Oncotarget 2015
25
18

Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicity.
Kristopher R Bosse, Sharon J Diskin, Kristina A Cole, Andrew C Wood, Robert W Schnepp, Geoffrey Norris, Le B Nguyen, Jayanti Jagannathan, Michael Laquaglia, Cynthia Winter,[...]. Cancer Res 2012
68
18

Integrative genomics identifies LMO1 as a neuroblastoma oncogene.
Kai Wang, Sharon J Diskin, Haitao Zhang, Edward F Attiyeh, Cynthia Winter, Cuiping Hou, Robert W Schnepp, Maura Diamond, Kristopher Bosse, Patrick A Mayes,[...]. Nature 2011
204
18

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.
Mario Capasso, Sharon Diskin, Flora Cimmino, Giovanni Acierno, Francesca Totaro, Giuseppe Petrosino, Lucia Pezone, Maura Diamond, Lee McDaniel, Hakon Hakonarson,[...]. Cancer Res 2014
67
18

Neuroblastoma in two siblings supports the role of 1p36 deletion in tumor development.
C Lo Cunsolo, A Iolascon, A Cavazzana, R Cusano, P Strigini, K Mazzocco, L Giordani, L Massimo, B De Bernardi, M Conte,[...]. Cancer Genet Cytogenet 1999
8
25

Genetics and genomics of neuroblastoma.
Mario Capasso, Sharon J Diskin. Cancer Treat Res 2010
59
18

Activating mutations in ALK provide a therapeutic target in neuroblastoma.
Rani E George, Takaomi Sanda, Megan Hanna, Stefan Fröhling, William Luther, Jianming Zhang, Yebin Ahn, Wenjun Zhou, Wendy B London, Patrick McGrady,[...]. Nature 2008
574
18

Weak linkage at 4p16 to predisposition for human neuroblastoma.
Patrizia Perri, Luca Longo, Roberto Cusano, Carmel M McConville, Sally A Rees, Marcella Devoto, Massimo Conte, Giovanni Battista Ferrara, Marco Seri, Giovanni Romeo,[...]. Oncogene 2002
29
18

Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition.
Antonella Gambale, Roberta Russo, Immacolata Andolfo, Lucia Quaglietta, Gianluca De Rosa, Valentina Contestabile, Lucia De Martino, Rita Genesio, Piero Pignataro, Sabrina Giglio,[...]. Clin Genet 2019
6
33

Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.
Sharon J Diskin, Mario Capasso, Robert W Schnepp, Kristina A Cole, Edward F Attiyeh, Cuiping Hou, Maura Diamond, Erica L Carpenter, Cynthia Winter, Hanna Lee,[...]. Nat Genet 2012
180
18


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.