A citation-based method for searching scientific literature

R van Zalen-Sprock, J M van Vugt, H J van der Harten, A W Nieuwint, H P van Geijn. J Ultrasound Med 1995
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


First-trimester ultrasound diagnosis of holoprosencephaly: three case reports.
H S Wong, Y H Lam, M H Tang, L W Cheung, L K Ng, K W Yan. Ultrasound Obstet Gynecol 1999
22
56

Early diagnosis of holoprosencephaly.
L H Nelson, M King. J Ultrasound Med 1992
24
50

Prenatal diagnosis of alobar holoprosencephaly at 10 weeks of gestation.
C D Turner, S Silva, P Jeanty. Ultrasound Obstet Gynecol 1999
18
50

First trimester diagnosis of holoprosencephaly with a Dandy-Walker malformation by transvaginal ultrasonography.
U Gembruch, A A Baschat, E Reusche, S J Wallner, M Greiwe. J Ultrasound Med 1995
11
63


Alobar holoprosencephaly at 9 weeks gestational age visualized by two- and three-dimensional ultrasound.
H G Blaas, S H Eik-Nes, T Vainio, C V Isaksen. Ultrasound Obstet Gynecol 2000
45
37

First trimester sonographic diagnosis of holoprosencephaly.
T Tongsong, C Wanapirak, P Chanprapaph, S Siriangkul. Int J Gynaecol Obstet 1999
12
50

First-trimester sonographic diagnosis of holoprosencephaly: value of the "butterfly" sign.
Waldo Sepulveda, Victor Dezerega, Cecilia Be. J Ultrasound Med 2004
45
37

Holoprosencephaly.
D M Peebles. Prenat Diagn 1998
36
31


Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases.
H G K Blaas, A G Eriksson, K A Salvesen, C V Isaksen, B Christensen, G Møllerløkken, S H Eik-Nes. Ultrasound Obstet Gynecol 2002
64
31

Diagnosis and management of fetal holoprosencephaly.
F A Chervenak, G Isaacson, J C Hobbins, U Chitkara, M Tortora, R L Berkowitz. Obstet Gynecol 1985
52
25

Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
40
25

[Prenatal diagnosis of holoprosencephaly. A series of twelve cases].
O Parant, M F Sarramon, M B Delisle, A Fournié. J Gynecol Obstet Biol Reprod (Paris) 1997
9
44

Alobar holoprosencephalic embryo detected via transvaginal sonography.
F González-Gómez, A Salamanca, M C Padilla, M Camara, R M Sabatel. Eur J Obstet Gynecol Reprod Biol 1992
9
44

Holoprosencephaly: prenatal sonographic diagnosis.
D A Nyberg, L A Mack, A Bronstein, J Hirsch, R A Pagon. AJR Am J Roentgenol 1987
48
25


Fetal holoprosencephaly: associated malformations and chromosomal defects.
S M Berry, C Gosden, R J Snijders, K H Nicolaides. Fetal Diagn Ther 1990
32
25

Three-dimensional sonographic evaluations of embryonic brain development.
Mi Suk Kim, Philippe Jeanty, Cheryl Turner, Bernard Benoit. J Ultrasound Med 2008
31
25


De novo 7q36 deletion: breakpoint analysis and types of holoprosencephaly.
S G Frints, E F Schoenmakers, E Smeets, P Petit, J P Fryns. Am J Med Genet 1998
24
18

Duplication 3p21----3pter and cyclopia.
D N Kurtzman, D L Van Dyke, C A Rich, L Weiss. Am J Med Genet 1987
25
18

Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly.
E Roessler, D E Ward, K Gaudenz, E Belloni, S W Scherer, D Donnai, J Siegel-Bartelt, L C Tsui, M Muenke. Hum Genet 1997
89
18

Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.
G H Vance, C Nickerson, L Sarnat, A Zhang, O Henegariu, N Morichon-Delvallez, M G Butler, C G Palmer. Am J Med Genet 1998
10
30

Pallister-Hall syndrome associated with an unbalanced chromosome translocation.
J A Kuller, V A Cox, S A Schonberg, M Golabi. Am J Med Genet 1992
31
18


Case of cyclopia with an unbalanced karyotype attributable to a balanced 3/7 translocation.
K F Bürrig, J Gebauer, R Terinde, P Pfitzer. Clin Genet 1989
16
18


Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
67
18

Early prenatal diagnosis of cyclopia associated with holoprosencephaly.
Z Tóth, K Csécsei, G Szeifert, O Török, Z Papp. J Clin Ultrasound 1986
11
27

Early development of the forebrain and midbrain: a longitudinal ultrasound study from 7 to 12 weeks of gestation.
H G Blaas, S H Eik-Nes, T Kiserud, L R Hellevik. Ultrasound Obstet Gynecol 1994
36
18

Intraventricular fused fornices: a specific sign of fetal lobar holoprosencephaly.
G Pilu, P Ambrosetto, F Sandri, G Tani, A Perolo, G Grisolia, G Ancora. Ultrasound Obstet Gynecol 1994
10
30

Diagnosis of fetal abnormalities at the 10-14-week scan.
A P Souka, K H Nicolaides. Ultrasound Obstet Gynecol 1997
64
18


Screening for fetal anomalies by ultrasound at 14 and 21 weeks.
G D'Ottavio, Y J Meir, M A Rustico, V Pecile, L Fischer-Tamaro, G Conoscenti, R Natale, G P Mandruzzato. Ultrasound Obstet Gynecol 1997
27
18

Detection of fetal structural abnormalities at the 11-14 week ultrasound scan.
M H B Carvalho, M L Brizot, L M Lopes, C H Chiba, S Miyadahira, M Zugaib. Prenat Diagn 2002
93
18

Fetal omphalocele detected early in pregnancy: associated anomalies and outcomes.
Shraga Blazer, Etan Z Zimmer, Ayala Gover, Moshe Bronshtein. Radiology 2004
45
18

Ultrasonographically detectable markers of fetal chromosomal abnormalities.
K H Nicolaides, R J Snijders, C M Gosden, C Berry, S Campbell. Lancet 1992
212
12

Reliable criteria for the prenatal sonographic diagnosis of alobar holoprosencephaly.
M F Greene, B R Benacerraf, F D Frigoletto. Am J Obstet Gynecol 1987
30
12

What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
12


Partial trisomy 3p in two siblings: clinical and pathological findings.
N Van Regemorter, E Vamos, Y Gillerot, V Viteux, F Hayez, A Pardou, J Flament-Durand. Eur J Pediatr 1983
21
12


Prenatal diagnosis of a dup(3p) with holoprosencephaly.
Y Gillerot, J Hustin, L Koulischer, V Viteux. Am J Med Genet 1987
21
12

[Familial occurrence of cyclops over several generations].
P Pfitzer, M Splitt, H Müntefering, J E Friesenecker. Verh Dtsch Ges Pathol 1982
6
33

Dup(3)(p2----pter) in two families, including one infant with cyclopia.
G Gimelli, C Cuoco, M Lituania, M Cordone, M Aricò, E Bianchi, P Maraschio, O Zuffardi. Am J Med Genet 1985
24
12

Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1.
N C Schanen, S W Scherer, L C Tsui, U Francke. Cytogenet Cell Genet 1996
12
16

Familial chromosome translocation t(3;18)(p21;p11).
G Buchinger, A Wettstein, H Metze. J Med Genet 1981
11
18

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
856
12

Criteria for the prenatal diagnosis of holoprosencephaly.
G Pilu, R Romero, N Rizzo, P Jeanty, L Bovicelli, J C Hobbins. Am J Perinatol 1987
23
12


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.