A citation-based method for searching scientific literature

Weimin Bi, Sau-Wai Cheung, Amy M Breman, Carlos A Bacino. Am J Med Genet A 2016
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome.
Karen S Ho, Sarah T South, Amanda Lortz, Charles H Hensel, Mallory R Sdano, Rena J Vanzo, Megan M Martin, Andreas Peiffer, Christophe G Lambert, Amy Calhoun,[...]. J Med Genet 2016
26
53

Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.
Marcella Zollino, Rosetta Lecce, Rita Fischetto, Marina Murdolo, Francesca Faravelli, Angelo Selicorni, Cinzia Buttè, Luigi Memo, Giuseppe Capovilla, Giovanni Neri. Am J Hum Genet 2003
146
46

On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
Marcella Zollino, Marina Murdolo, Giuseppe Marangi, Vanna Pecile, Cinzia Galasso, Laura Mazzanti, Giovanni Neri. Am J Med Genet C Semin Med Genet 2008
95
46

Wolf-Hirschhorn syndrome: A review and update.
Agatino Battaglia, John C Carey, Sarah T South. Am J Med Genet C Semin Med Genet 2015
65
46

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region.
T J Wright, D O Ricke, K Denison, S Abmayr, P D Cotter, K Hirschhorn, M Keinänen, D McDonald-McGinn, M Somer, N Spinner,[...]. Hum Mol Genet 1997
174
46

Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome.
Erica F Andersen, John C Carey, Dawn L Earl, Deyanira Corzo, Michael Suttie, Peter Hammond, Sarah T South. Eur J Hum Genet 2014
24
38

Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
Marcella Zollino, Daniela Orteschi, Mariken Ruiter, Rolph Pfundt, Katharina Steindl, Concetta Cafiero, Stefania Ricciardi, Ilaria Contaldo, Daniela Chieffo, Domiziana Ranalli,[...]. Epilepsia 2014
17
38

Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.
K Hirschhorn, H L Cooper, I L Firschein. Humangenetik 1965
237
38

A histone H3 lysine 36 trimethyltransferase links Nkx2-5 to Wolf-Hirschhorn syndrome.
Keisuke Nimura, Kiyoe Ura, Hidetaka Shiratori, Masato Ikawa, Masaru Okabe, Robert J Schwartz, Yasufumi Kaneda. Nature 2009
252
38


Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH).
N M C Maas, G Van Buggenhout, F Hannes, B Thienpont, D Sanlaville, K Kok, A Midro, J Andrieux, B-M Anderlid, J Schoumans,[...]. J Med Genet 2008
85
30

[Deficiency on the short arms of a chromosome No. 4].
U Wolf, H Reinwein, R Porsch, R Schröter, H Baitsch. Humangenetik 1965
236
30

109 kb deletion of chromosome 4p16.3 in a patient with mild phenotype of Wolf-Hirschhorn syndrome.
Nobuhiko Okamoto, Kazumi Ohmachi, Shino Shimada, Keiko Shimojima, Toshiyuki Yamamoto. Am J Med Genet A 2013
12
33

LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability.
Kai Stefan Dimmer, Francesca Navoni, Alberto Casarin, Eva Trevisson, Sabine Endele, Andreas Winterpacht, Leonardo Salviati, Luca Scorrano. Hum Mol Genet 2008
131
30

First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation.
A Rauch, S Schellmoser, C Kraus, H G Dörr, U Trautmann, M R Altherr, R A Pfeiffer, A Reis. Am J Med Genet 2001
92
23

Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.
Kenji Shimizu, Keiko Wakui, Tomoki Kosho, Nobuhiko Okamoto, Seiji Mizuno, Kazuya Itomi, Shigeto Hattori, Kimio Nishio, Osamu Samura, Yoshiyuki Kobayashi,[...]. Am J Med Genet A 2014
14
23

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.
M Zollino, C Di Stefano, G Zampino, P Mastroiacovo, T J Wright, G Sorge, A Selicorni, R Tenconi, A Zappalà, A Battaglia,[...]. Am J Med Genet 2000
116
23


Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map.
G Van Buggenhout, C Melotte, B Dutta, G Froyen, P Van Hummelen, P Marynen, G Matthijs, T de Ravel, K Devriendt, J P Fryns,[...]. J Med Genet 2004
97
23

Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.
Sarah T South, Heidi Whitby, Agatino Battaglia, John C Carey, Arthur R Brothman. Eur J Hum Genet 2008
50
23

Wolf-Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions.
Hannelie Engbers, Jasper J van der Smagt, Ruben van 't Slot, Joris R Vermeesch, Ron Hochstenbach, Martin Poot. Eur J Hum Genet 2009
41
23

Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia.
Periklis Makrythanasis, Mitsuhiro Kato, Maha S Zaki, Hirotomo Saitsu, Kazuyuki Nakamura, Federico A Santoni, Satoko Miyatake, Mitsuko Nakashima, Mahmoud Y Issa, Michel Guipponi,[...]. Am J Hum Genet 2016
51
23


Multiple congenital malformations of Wolf-Hirschhorn syndrome are recapitulated in Fgfrl1 null mice.
Catarina Catela, Daniel Bilbao-Cortes, Esfir Slonimsky, Paschalis Kratsios, Nadia Rosenthal, Pascal Te Welscher. Dis Model Mech 2009
58
23

C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development.
Sabine Endele, Claudia Nelkenbrecher, Annegret Bördlein, Stefanie Schlickum, Andreas Winterpacht. Neurogenetics 2011
5
60

Mouse models of Wolf-Hirschhorn syndrome.
Ruth Simon, Andrew D Bergemann. Am J Med Genet C Semin Med Genet 2008
20
23

Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirschhorn syndrome.
Claudia Kerzendorfer, Femke Hannes, Rita Colnaghi, Iga Abramowicz, Gillian Carpenter, Joris Robert Vermeesch, Mark O'Driscoll. Hum Mol Genet 2012
35
23

NELF interacts with CBC and participates in 3' end processing of replication-dependent histone mRNAs.
Takashi Narita, Tetsu M C Yung, Junichi Yamamoto, Yasunori Tsuboi, Hideyuki Tanabe, Kiyoji Tanaka, Yuki Yamaguchi, Hiroshi Handa. Mol Cell 2007
154
23


The Wolf-Hirschhorn syndrome. I. Genetics.
I W Lurie, G I Lazjuk, Y I Ussova, E B Presman, D B Gurevich. Clin Genet 1980
106
15

The new Wolf-Hirschhorn syndrome critical region (WHSCR-2): a description of a second case.
Laura Rodríguez, Marcella Zollino, Salvador Climent, Elena Mansilla, Fermina López-Grondona, María Luisa Martínez-Fernández, Marina Murdolo, María Luisa Martínez-Frías. Am J Med Genet A 2005
35
15

An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality.
N L Shannon, E L Maltby, A S Rigby, O W Quarrell. J Med Genet 2001
48
15

Comparative analysis of a novel gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks syndrome critical region.
T J Wright, J L Costa, C Naranjo, P Francis-West, M R Altherr. Genomics 1999
49
15

Diagnosis and fine localization of deletion region in Wolf-Hirschhorn syndrome patients.
Tao-Yun Ji, David Chia, Jing-Min Wang, Ye Wu, Jie Li, Jing Xiao, Yu-Wu Jiang. Chin Med J (Engl) 2010
6
33

Prenatal diagnosis of Wolf-Hirschhorn syndrome: ultrasonography and genetics.
Thomas Ikonomou, Panos Antsaklis, Georgios Daskalakis, Michael Sindos, Nikolaos Papantoniou, Zoi Kosmaidou, Aris Antsaklis. J Matern Fetal Neonatal Med 2013
6
33


Complexins regulate a late step in Ca2+-dependent neurotransmitter release.
K Reim, M Mansour, F Varoqueaux, H T McMahon, T C Südhof, N Brose, C Rosenmund. Cell 2001
338
15

Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.
Anne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, Pierre Déchelotte, Anne-Marie Beaufrère, Didier Lémery, Christine Francannet, Denis Gallot. Birth Defects Res A Clin Mol Teratol 2013
4
50

The centrosomal protein TACC3 is essential for hematopoietic stem cell function and genetically interfaces with p53-regulated apoptosis.
Roland P Piekorz, Angelika Hoffmeyer, Christopher D Duntsch, Catriona McKay, Hideaki Nakajima, Veronika Sexl, Linda Snyder, Jerold Rehg, James N Ihle. EMBO J 2002
94
15

Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene.
Baran Bayindir, Elena Piazza, Erika Della Mina, Ivan Limongelli, Francesca Brustia, Roberto Ciccone, Pierangelo Veggiotti, Orsetta Zuffardi, Mohammed Reza Dehghani. Eur J Med Genet 2013
9
22


Deletion of a 760 kb region at 4p16 determines the prenatal and postnatal growth retardation characteristic of Wolf-Hirschhorn syndrome.
Daniela Concolino, Elena Rossi, Pietro Strisciuglio, Maria Antonietta Iembo, Roberto Giorda, Roberto Ciccone, Romano Tenconi, Orsetta Zuffardi. J Med Genet 2007
17
15

Cytoscape: a software environment for integrated models of biomolecular interaction networks.
Paul Shannon, Andrew Markiel, Owen Ozier, Nitin S Baliga, Jonathan T Wang, Daniel Ramage, Nada Amin, Benno Schwikowski, Trey Ideker. Genome Res 2003
15

The etiology of Wolf-Hirschhorn syndrome.
Andrew D Bergemann, Francesca Cole, Kurt Hirschhorn. Trends Genet 2005
110
15

Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3.
Sarah T South, Femke Hannes, Gene S Fisch, Joris Robert Vermeesch, Marcella Zollino. Am J Med Genet C Semin Med Genet 2008
31
15

Wolf-Hirschhorn (4p-) syndrome.
A Battaglia, J C Carey, T J Wright. Adv Pediatr 2001
68
15

Congenital diaphragmatic hernia and a complex heart defect in association with Wolf-Hirschhorn syndrome.
Juliane Tautz, Danielle Veenma, Bert Eussen, Linda Joosen, Pino Poddighe, Dick Tibboel, Annelies de Klein, Thomas Schaible. Am J Med Genet A 2010
8
25

Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay.
Femke Hannes, Malgorzata Drozniewska, Joris R Vermeesch, Olga Haus. Eur J Med Genet 2010
15
15

The TACC proteins: TACC-ling microtubule dynamics and centrosome function.
Isabel Peset, Isabelle Vernos. Trends Cell Biol 2008
115
15

A Drosophila mutant of LETM1, a candidate gene for seizures in Wolf-Hirschhorn syndrome.
Angus G McQuibban, Nicholas Joza, Aram Megighian, Michele Scorzeto, Damiano Zanini, Siegfried Reipert, Constance Richter, Rudolf J Schweyen, Karin Nowikovsky. Hum Mol Genet 2010
51
15


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.