A citation-based method for searching scientific literature

S Beaudoin, A Mathiot-Gavarin, G Gouizi, F Bargy. Pediatr Surg Int 2005
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Jack Barney Award. The changing spectrum of intestinal malrotation: diagnosis and management.
Marcene R McVay, Evan R Kokoska, Richard J Jackson, Samuel D Smith. Am J Surg 2007
42
75

Familial midgut volvulus.
S L Smith. Surgery 1972
12
75

Malrotation of the intestine.
A M Torres, M M Ziegler. World J Surg 1993
149
50

Malrotation - the ubiquitous anomaly.
H C Filston, D R Kirks. J Pediatr Surg 1981
99
50

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
262
50


The chirality of gut rotation derives from left-right asymmetric changes in the architecture of the dorsal mesentery.
Nicole M Davis, Natasza A Kurpios, Xiaoxia Sun, Jerome Gros, James F Martin, Clifford J Tabin. Dev Cell 2008
96
50


Review of genetic factors in intestinal malrotation.
Vicki Martin, Charles Shaw-Smith. Pediatr Surg Int 2010
43
50

The diagnostic value of the triple bubble sign in proximal jejunal atresia: a case report.
A O D Amole, A W B R Johnson, O A M Adesiyun. Afr J Med Med Sci 2003
1
100



Triple bubble sign: a marker of proximal jejunal atresia.
T Tongsong, P Chanprapaph. Int J Gynaecol Obstet 2000
3
33

Multiple atresias and a new syndrome of hereditary multiple atresias involving the gastrointestinal tract from stomach to rectum.
F M Guttman, P Braun, P H Garance, H Blanchard, P P Collin, L Dallaire, J G Desjardins, G Perreault. J Pediatr Surg 1973
106
25


Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB.
R Kosaki, M Gebbia, K Kosaki, M Lewin, P Bowers, J A Towbin, B Casey. Am J Med Genet 1999
138
25

Malrotation of the bowel in infants and children: a 15 year review.
D R Stewart, A L Colodny, W C Daggett. Surgery 1976
112
25

Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement.
Annagiusi Gargiulo, Renata Auricchio, Maria Vittoria Barone, Gabriella Cotugno, William Reardon, Peter J Milla, Andrea Ballabio, Alfredo Ciccodicola, Alberto Auricchio. Am J Hum Genet 2007
66
25


Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies.
Sevim Balci, Ozlem Engiz, Dilek Aktaş, Ibrahim Vargel, M S Beksaç, Kristin Mrasek, Joris Vermeesch, Thomas Liehr. Am J Med Genet A 2006
20
25

Tracheoesophageal fistula, gastrointestinal abnormalities, hypospadias, and prenatal growth deficiency.
M L Martínez-Frías, J L Frías, E Galán, R Domingo, L Paisán, M Blanco. Am J Med Genet 1992
23
25

Partial deletion of 4p and 4q in a fetus with ring chromosome 4: phenotype and molecular mapping of the breakpoints.
A Kocks, S Endele, R Heller, B Schröder, H-J Schäfer, C Städtler, M Makrigeorgi-Butera, A Winterpacht. J Med Genet 2002
18
25

Ring chromosome 4 in a child with duodenal atresia.
F Halal, M Vekemans. Am J Med Genet 1990
12
25

Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects.
Stephanie M Ware, Jianlan Peng, Lirong Zhu, Susan Fernbach, Suzanne Colicos, Brett Casey, Jeffrey Towbin, John W Belmont. Am J Hum Genet 2004
172
25

Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13.
A Shanske, J C Ferreira, J C Leonard, P Fuller, R W Marion. Am J Med Genet 2001
35
25

Serpentine fibula syndrome: expansion of the phenotype with three affected siblings.
E M Rosser, N P Mann, C M Hall, R M Winter. Clin Dysmorphol 1996
17
25

Second family with "apple peel" syndrome affecting four siblings: autosomal recessive inheritance confirmed.
T I Farag, S A al-Awadi, M H el-Badramany, R Usha, M el-Ghanem. Am J Med Genet 1993
13
25

Cytogenetic technology--genotype and phenotype.
David H Ledbetter. N Engl J Med 2008
30
25


A further example of a distinctive autosomal recessive syndrome comprising neonatal diabetes mellitus, intestinal atresias and gall bladder agenesis.
Louise Chappell, Shaun Gorman, Fiona Campbell, Sian Ellard, Gillian Rice, Angus Dobbie, Yanick Crow. Am J Med Genet A 2008
27
25

X-linked situs abnormalities result from mutations in ZIC3.
M Gebbia, G B Ferrero, G Pilia, M T Bassi, A Aylsworth, M Penman-Splitt, L M Bird, J S Bamforth, J Burn, D Schlessinger,[...]. Nat Genet 1997
304
25

Hardikar syndrome: new features.
J Rainer Poley, Virginia K Proud. Am J Med Genet A 2008
5
25



Triphalangeal thumb in a case of VACTERL-hydrocephalus association.
S Balci, M E Senocak, M Derbent. Genet Couns 2003
6
25

Limb body wall complex: analysis of eight fetuses.
V Cusí, M Torrents, J Vila, J Antich, J M Carrera. Birth Defects Orig Artic Ser 1996
4
25


Familial jejunal atresia: three cases in one family.
H G Mishalany, F B Najjar. J Pediatr 1968
53
25




Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.
A Slavotinek, S S Lee, R Davis, A Shrit, K A Leppig, J Rhim, K Jasnosz, D Albertson, D Pinkel. J Med Genet 2005
75
25


Hereditary multiple intestinal atresia.
L Dallaire, G Perreault. Birth Defects Orig Artic Ser 1974
18
25

Exclusion of a PAX6, FOXC1, PITX2, and MYCN mutation in another patient with apple peel intestinal atresia, ocular anomalies and microcephaly and review of the literature.
Yolande van Bever, Liselotte van Hest, Roger Wolfs, Dick Tibboel, Thelma L van den Hoonaard, Saskia J Gischler. Am J Med Genet A 2008
10
25


Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects.
R N Bamford, E Roessler, R D Burdine, U Saplakoğlu, J dela Cruz, M Splitt, J A Goodship, J Towbin, P Bowers, G B Ferrero,[...]. Nat Genet 2000
231
25

Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
S Brisset, G Joly, C Ozilou, J-M Lapierre, Ph Gosset, M LeLorc'h, O Raoul, C Turleau, M Vekemans, S P Romana. Am J Med Genet 2002
38
25


De novo trisomy 16p11.2-qter: report of an infant.
M Masuno, T Ishii, Y Tanaka, M Ohyama, M Kawataki, J Kimura, K Imaizumi, Y Kuroki. Am J Med Genet 2000
14
25


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.