A citation-based method for searching scientific literature

Johanna Winberg, Peter Gustavsson, Nikos Papadogiannakis, Ellika Sahlin, Frideborg Bradley, Edvard Nordenskjöld, Pär-Johan Svensson, Göran Annerén, Erik Iwarsson, Ann Nordgren, Agneta Nordenskjöld. PLoS One 2014
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


VACTERL/VATER Association.
Benjamin D Solomon. Orphanet J Rare Dis 2011
190
45

Identification of a HOXD13 mutation in a VACTERL patient.
Maria-Mercè Garcia-Barceló, Kenneth Kak-yuen Wong, Vincent Chi-hang Lui, Zhen-wei Yuan, Man-ting So, Elly Sau-wai Ngan, Xiao-ping Miao, Patrick Ho-yu Chung, Pek-lan Khong, Paul Kwong-hang Tam. Am J Med Genet A 2008
61
40

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.
Pawaree Saisawat, Stefan Kohl, Alina C Hilger, Daw-Yang Hwang, Heon Yung Gee, Gabriel C Dworschak, Velibor Tasic, Tracie Pennimpede, Sivakumar Natarajan, Ethan Sperry,[...]. Kidney Int 2014
72
40

VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5.
Dorota Szumska, Guido Pieles, Rachid Essalmani, Michal Bilski, Daniel Mesnard, Kulvinder Kaur, Angela Franklyn, Kamel El Omari, Joanna Jefferis, Jamie Bentham,[...]. Genes Dev 2008
89
40

Evidence for inheritance in patients with VACTERL association.
Benjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, Derek A T Cummings. Hum Genet 2010
51
40

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.
Alina Hilger, Charlotte Schramm, Tracie Pennimpede, Lars Wittler, Gabriel C Dworschak, Enrika Bartels, Hartmut Engels, Alexander M Zink, Franziska Degenhardt, Annette M Müller,[...]. Eur J Hum Genet 2013
30
35

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
Paweł Stankiewicz, Partha Sen, Samarth S Bhatt, Mekayla Storer, Zhilian Xia, Bassem A Bejjani, Zhishuo Ou, Joanna Wiszniewska, Daniel J Driscoll, Melissa K Maisenbacher,[...]. Am J Hum Genet 2009
259
35

Familial occurrence of the VATER/VACTERL association.
Alina Hilger, Charlotte Schramm, Markus Draaken, Sadaf S Mughal, Gabriel Dworschak, Enrika Bartels, Per Hoffmann, Markus M Nöthen, Heiko Reutter, Michael Ludwig. Pediatr Surg Int 2012
26
30

De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations.
Gabriel C Dworschak, Markus Draaken, Carlo Marcelis, Ivo de Blaauw, Rolph Pfundt, Iris A L M van Rooij, Enrika Bartels, Alina Hilger, Ekkehart Jenetzky, Eberhard Schmiedeke,[...]. Am J Med Genet A 2013
25
30

The spectrum of congenital anomalies of the VATER association: an international study.
L D Botto, M J Khoury, P Mastroiacovo, E E Castilla, C A Moore, R Skjaerven, O M Mutchinick, B Borman, G Cocchi, A E Czeizel,[...]. Am J Med Genet 1997
166
30

De novo microduplication at 22q11.21 in a patient with VACTERL association.
Charlotte Schramm, Markus Draaken, Enrika Bartels, Thomas M Boemers, Stefan Aretz, Felix F Brockschmidt, Markus M Nöthen, Michael Ludwig, Heiko Reutter. Eur J Med Genet 2011
45
30

Clinical geneticists' views of VACTERL/VATER association.
Benjamin D Solomon, Kelly A Bear, Virginia Kimonis, Annelies de Klein, Daryl A Scott, Charles Shaw-Smith, Dick Tibboel, Heiko Reutter, Philip F Giampietro. Am J Med Genet A 2012
47
30



A population study of the VACTERL association: evidence for its etiologic heterogeneity.
M J Khoury, J F Cordero, F Greenberg, L M James, J D Erickson. Pediatrics 1983
237
25



Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.
Alina C Hilger, Jan Halbritter, Tracie Pennimpede, Amelie van der Ven, Georgia Sarma, Daniela A Braun, Jonathan D Porath, Stefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak,[...]. Hum Mutat 2015
28
25

Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome.
S T Holden, J J Cox, I Kesterton, N S Thomas, C Carr, C G Woods. J Med Genet 2006
49
25

From VACTERL-H to heterotaxy: variable expressivity of ZIC3-related disorders.
Brian Chung, Lisa G Shaffer, Sarah Keating, Joan Johnson, Bret Casey, David Chitayat. Am J Med Genet A 2011
40
20

Considering the Embryopathogenesis of VACTERL Association.
R E Stevenson, A G W Hunter. Mol Syndromol 2013
34
20

Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis.
Sirisha Peddibhotla, Mohamed Khalifa, Frank J Probst, Jennifer Stein, Leslie L Harris, Debra L Kearney, Gail H Vance, Marilyn J Bull, Dorothy K Grange, Gunter H Scharer,[...]. Am J Med Genet A 2013
16
25

Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?
Marja W Wessels, Brian Kuchinka, Rogier Heydanus, Bert J Smit, Dennis Dooijes, Ronald R de Krijger, Maarten H Lequin, Elisabeth M de Jong, Margreet Husen, Patrick J Willems,[...]. J Med Genet 2010
55
20

X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations.
Joanna McCauley, Navta Masand, Ruth McGowan, Sulekha Rajagopalan, Alasdair Hunter, Jacques L Michaud, Kate Gibson, Jeremy Robertson, Fiona Vaz, Stephen Abbs,[...]. Am J Med Genet A 2011
30
20

Long-term outcomes of adults with features of VACTERL association.
Manu S Raam, Daniel E Pineda-Alvarez, Donald W Hadley, Benjamin D Solomon. Eur J Med Genet 2011
28
20

VATER non-random association of congenital malformations: study based on data from four malformation registers.
K Källén, P Mastroiacovo, E E Castilla, E Robert, B Källén. Am J Med Genet 2001
82
20

Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
Claudia Zeidler, Joachim Woelfle, Markus Draaken, Sadaf S Mughal, Greta Große, Alina C Hilger, Gabriel C Dworschak, Thomas M Boemers, Ekkehart Jenetzky, Nadine Zwink,[...]. Birth Defects Res A Clin Mol Teratol 2014
14
28

Analysis of component findings in 79 patients diagnosed with VACTERL association.
Benjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, Sophia M Bous, Amelia A Keaton, Jorge I Vélez, Derek A T Cummings. Am J Med Genet A 2010
53
20

PCSK5 mutation in a patient with the VACTERL association.
Yukio Nakamura, Shingo Kikugawa, Shoji Seki, Masahiko Takahata, Norimasa Iwasaki, Hidetomi Terai, Mitsuhiro Matsubara, Fumio Fujioka, Hidehito Inagaki, Tatsuya Kobayashi,[...]. BMC Res Notes 2015
9
44

VACTERL-H Association and Fanconi Anemia.
B P Alter, P S Rosenberg. Mol Syndromol 2013
39
20


An aetiological study of the VACTERL-association.
A Czeizel, I Ludányi. Eur J Pediatr 1985
86
15


VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis.
Enrika Bartels, Anna C Schulz, Nicole W Mora, Daniel E Pineda-Alvarez, Charlotte H W Wijers, Carlo M Marcelis, Rüdiger Stressig, Jochen Ritgen, Eberhard Schmiedeke, Manuel Mattheisen,[...]. Clin Dysmorphol 2012
13
23

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
516
15



5q11.2 deletion in a patient with tracheal agenesis.
Elisabeth M de Jong, Hannie Douben, Bert H Eussen, Janine F Felix, Marja W Wessels, Pino J Poddighe, Peter G J Nikkels, Ronald R de Krijger, Dick Tibboel, Annelies de Klein. Eur J Hum Genet 2010
26
15

Should chromosome breakage studies be performed in patients with VACTERL association?
Laurence Faivre, Marie France Portnoï, Gerard Pals, Dominique Stoppa-Lyonnet, Martine Le Merrer, Christel Thauvin-Robinet, Frédéric Huet, Christopher G Mathew, Hans Joenje, Alain Verloes,[...]. Am J Med Genet A 2005
53
15

Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association.
Andrés Hernández-García, Erwin Brosens, Hitisha P Zaveri, Elisabeth M de Jong, Zhiyin Yu, Maria Namwanje, Allison Mayle, Caraciolo J Fernandes, Brendan Lee, Maria Blazo,[...]. Am J Med Genet A 2012
8
37

Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies.
Lars T van der Veken, Marianne Mj Dieleman, Hannie Douben, Judith C van de Brug, Raoul van de Graaf, A Jeannette M Hoogeboom, Pino J Poddighe, Annelies de Klein. Mol Cytogenet 2010
21
15

VACTERL association, epidemiologic definition and delineation.
M Rittler, J E Paz, E E Castilla. Am J Med Genet 1996
112
15

Sonic hedgehog mutation analysis in patients with VACTERL association.
Mónica Aguinaga, Juan Carlos Zenteno, Héctor Pérez-Cano, Verónica Morán. Am J Med Genet A 2010
23
15

VACTERL association and maternal diabetes: a possible causal relationship?
Marco Castori, Rosanna Rinaldi, Paolo Capocaccia, Mario Roggini, Paola Grammatico. Birth Defects Res A Clin Mol Teratol 2008
30
15

Clinical characteristics of neonates with VACTERL association.
Akgun Oral, Ibrahim Caner, Murat Yigiter, Mecit Kantarci, Hasim Olgun, Naci Ceviz, Ahmet Bedii Salman. Pediatr Int 2012
18
16

X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.
Barbara Mikat, Claudia Roll, Detlev Schindler, Ulrich Gembruch, Iris Klempert, Karin Buiting, Nuria C Bramswig, Dagmar Wieczorek. Clin Dysmorphol 2016
8
37


SnapShot: Fanconi anemia and associated proteins.
Anderson T Wang, Agata Smogorzewska. Cell 2015
97
15

Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.
Heiko Reutter, Alina C Hilger, Friedhelm Hildebrandt, Michael Ludwig. Pediatr Nephrol 2016
15
20

Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalities.
Gabriel C Dworschak, Markus Draaken, Alina C Hilger, Charlotte Schramm, Enrika Bartels, Eberhard Schmiedeke, Sabine Grasshoff-Derr, Stefanie Märzheuser, Stefan Holland-Cunz, Martin Lacher,[...]. Birth Defects Res A Clin Mol Teratol 2015
13
23


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.