A citation-based method for searching scientific literature

M I Van Allen, S Ritchie, A Toi, K Fong, E Winsor. Am J Med Genet 1993
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Pre- and postnatal diagnosis of trisomy 4 mosaicism.
J P Marion, P M Fernhoff, J Korotkin, J H Priest. Am J Med Genet 1990
23
58

Prenatal diagnosis of trisomy 4 mosaicism.
A L Zaslav, D Blumenthal, J P Willner, G Pierno, J Jacob, J E Fox. Am J Med Genet 2000
11
45

Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy.
B D Kuchinka, I J Barrett, G Moya, J M Sánchez, S Langlois, S L Yong, D K Kalousek, W P Robinson. Prenat Diagn 2001
24
41

Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
Dagmar Wieczorek, Eva C Prott, Wendy P Robinson, Eberhard Passarge, Gabriele Gillessen-Kaesbach. Prenat Diagn 2003
12
41

Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.
L Y Hsu, M T Yu, R L Neu, D L Van Dyke, P A Benn, C L Bradshaw, L G Shaffer, R R Higgins, G S Khodr, C C Morton,[...]. Prenat Diagn 1997
135
33

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.
W P Robinson, I J Barrett, L Bernard, A Telenius, F Bernasconi, R D Wilson, R G Best, P N Howard-Peebles, S Langlois, D K Kalousek. Am J Hum Genet 1997
161
25

Cytogenetic results from the U.S. Collaborative Study on CVS.
D H Ledbetter, J M Zachary, J L Simpson, M S Golbus, E Pergament, L Jackson, M J Mahoney, R J Desnick, J Schulman, K L Copeland. Prenat Diagn 1992
273
25

Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Tung-Yao Chang, Wayseen Wang, Chin-Yuan Tzen. Prenat Diagn 2004
8
37

Mosaic trisomy 4: Long-term outcome on the first reported liveborn.
April N Brady, Kristin M May, Paul M Fernhoff. Am J Med Genet A 2005
9
33


Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment.
W P Robinson, F Bernasconi, A Lau, D E McFadden. Am J Med Genet 1999
31
16


Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.
W P Robinson, F Binkert, F Bernasconi, I Lorda-Sanchez, E A Werder, A A Schinzel. Am J Hum Genet 1995
107
16


Human aneuploidy: incidence, origin, and etiology.
T Hassold, M Abruzzo, K Adkins, D Griffin, M Merrill, E Millie, D Saker, J Shen, M Zaragoza. Environ Mol Mutagen 1996
298
16

Case of atypical cyclopia.
J Zheng, S Zhang. Oral Surg Oral Med Oral Pathol 1991
4
50

Cyclopia and congenital cytomegalovirus infection.
P J Byrne, M M Silver, J M Gilbert, W Cadera, A K Tanswell. Am J Med Genet 1987
41
16

Inherited pericentric inversion of chromosome no. 4.
M G Wilson, J W Towner, G S Coffin, I Forsman. Am J Hum Genet 1970
48
16

Clinical manifestations of trisomy 4p syndrome.
S V Patel, H Dagnew, A J Parekh, E Koenig, R A Conte, M J Macera, R S Verma. Eur J Pediatr 1995
45
16


The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32.
S Brown, J Russo, D Chitayat, D Warburton. Am J Hum Genet 1995
146
16

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
843
16


Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization.
Mattia Gentile, Paolo Volpe, Filomena Cariola, Antonio Di Carlo, Vincenzo Marotta, Antonia Lucia Buonadonna, Filippo Maria Boscia. Am J Med Genet A 2005
7
28

Confined placental mosaicism.
G Simoni, S M Sirchia. Prenat Diagn 1994
35
16

Does confined placental mosaicism affect the fetus?
G Simoni, M Fraccaro. Hum Reprod 1992
14
16

Trophoblastic oxidative stress and the release of cell-free feto-placental DNA.
May Lee Tjoa, Tereza Cindrova-Davies, Olivera Spasic-Boskovic, Diana W Bianchi, Graham J Burton. Am J Pathol 2006
146
16

Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results.
Francesca R Grati, Francesca Malvestiti, Jose C P B Ferreira, Komal Bajaj, Elisa Gaetani, Cristina Agrati, Beatrice Grimi, Francesca Dulcetti, Anna M Ruggeri, Simona De Toffol,[...]. Genet Med 2014
118
16


Application of a new molecular technique for the genetic evaluation of products of conception.
Francesca R Grati, Denise Molina Gomes, Devika Ganesamoorthy, Livia Marcato, Simona De Toffol, Eleonore Blondeel, Francesca Malvestiti, Laurence Loeuillet, Anna Maria Ruggeri, Robert Wainer,[...]. Prenat Diagn 2013
13
16





Distribution of mosaicism in human placentae.
K G Henderson, T E Shaw, I J Barrett, A H Telenius, R D Wilson, D K Kalousek. Hum Genet 1996
53
8

A homozygote for pericentric inversion of chromosome 4.
N J Carpenter, B Say, N D Barber. J Med Genet 1982
24
8

Cytogenetic analysis of 2928 CVS samples and 1075 amniocenteses from randomized studies.
S Smidt-Jensen, A M Lind, M Permin, J M Zachary, C Lundsteen, J Philip. Prenat Diagn 1993
32
8

The utilization of interphase cytogenetic analysis for the detection of mosaicism.
B L Lomax, D K Kalousek, B D Kuchinka, I J Barrett, K J Harrison, H Safavi. Hum Genet 1994
41
8


Trisomy 4: an entity within acute nonlymphocytic leukemia.
A A Sandberg, R Morgan, S N Sait, R Berger, G Flandrin, S Schrier, F Hecht. Cancer Genet Cytogenet 1987
57
8

Patient with trisomy 6 mosaicism.
K R Miller, K Mühlhaus, R A Herbst, B Bohnhorst, S Böhmer, M Arslan-Kirchner. Am J Med Genet 2001
13
8


Linear nevus sebaceus with convulsions and mental retardation.
R C FEUERSTEIN, L C MIMS. Am J Dis Child 1962
198
8

Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage.
B Eiben, I Bartels, S Bähr-Porsch, S Borgmann, G Gatz, G Gellert, R Goebel, W Hammans, M Hentemann, R Osmers. Am J Hum Genet 1990
199
8

Holoprosencephaly: the Maastricht experience.
U Moog, C E De Die-Smulders, C T Schrander-Stumpel, J J Engelen, A J Hamers, S Frints, J P Fryns. Genet Couns 2001
22
8

Trisomy D and the cyclops malformation.
K Taysi, K Tinaztepe. Am J Dis Child 1972
24
8


Molecular genetics of holoprosencephaly.
L Nanni, R L Schelper, M T Muenke. Front Biosci 2000
24
8

Trisomy-D in a cyclops with cardiovascular defects.
O E Jaschevatzky, B Goldman, P Georghiou, S Grünstein, S Pevzner. Acta Obstet Gynecol Scand 1976
3
33

Cyclopia and other anomalies following maternal ingestion of salicylates.
R Benawra, H H Mangurten, D R Duffell. J Pediatr 1980
47
8


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.