A citation-based method for searching scientific literature

L L Estabrooks, K W Rao, R P Donahue, A S Aylsworth. Am J Med Genet 1990
Times Cited: 41







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



Times Cited
  Times     Co-cited
Similarity


A male infant with holoprosencephaly, associated with ring chromosome 21.
D C Aronson, M C Jansweijer, J M Hoovers, P G Barth. Clin Genet 1987
24
58

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.
M J McGinniss, H H Kazazian, G Stetten, M B Petersen, H Boman, E Engel, F Greenberg, J M Hertz, A Johnson, Z Laca. Am J Hum Genet 1992
86
29


Physical findings in 21q22 deletion suggest critical region for 21q- phenotype in q22.
D S Theodoropoulos, J M Cowan, E R Elias, C Cole. Am J Med Genet 1995
31
32

Continuum of overlapping clones spanning the entire human chromosome 21q.
I Chumakov, P Rigault, S Guillou, P Ougen, A Billaut, G Guasconi, P Gervy, I LeGall, P Soularue, L Grinas. Nature 1992
464
21

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.
Z Rahmani, J L Blouin, N Creau-Goldberg, P C Watkins, J F Mattei, M Poissonnier, M Prieur, Z Chettouh, A Nicole, A Aurias. Proc Natl Acad Sci U S A 1989
232
21

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.
Z Chettouh, M F Croquette, B Delobel, S Gilgenkrants, C Leonard, C Maunoury, M Prieur, M O Rethoré, P M Sinet, M Chery. Am J Hum Genet 1995
68
19

A case of 21q--syndrome with normal SOD-1 activity.
Y Yamamoto, N Ogasawara, A Gotoh, H Komiya, H Nakai, Y Kuroki. Hum Genet 1979
45
19

Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion.
J R Korenberg, D K Kalousek, G Anneren, S M Pulst, J G Hall, C J Epstein, D R Cox. Hum Genet 1991
45
19

A NotI restriction map of the entire long arm of human chromosome 21.
H Ichikawa, F Hosoda, Y Arai, K Shimizu, M Ohira, M Ohki. Nat Genet 1993
105
17

Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.
J R Korenberg, H Kawashima, S M Pulst, T Ikeuchi, N Ogasawara, K Yamamoto, S A Schonberg, R West, L Allen, E Magenis. Am J Hum Genet 1990
188
17

Physical mapping of the holoprosencephaly critical region in 18p11.3.
J Overhauser, H F Mitchell, E H Zackai, D B Tick, K Rojas, M Muenke. Am J Hum Genet 1995
93
17

Holoprosencephaly associated with ring chromosome 21.
J M Hoovers, M C Jansweijer. Clin Genet 1987
10
70

Monosomy 21q: two cases of del(21q) and review of the literature.
J L Huret, C Léonard, M Chery, C Philippe, E Schafei-Benaissa, G Lefaure, B Labrune, S Gilgenkrantz. Clin Genet 1995
42
17

Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.
A E Lehesjoki, M Koskiniemi, P Sistonen, J Miao, J Hästbacka, R Norio, A de la Chapelle. Proc Natl Acad Sci U S A 1991
170
17


Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.
J R Korenberg, C Bradley, C M Disteche. Am J Hum Genet 1992
130
14

Down syndrome phenotypes: the consequences of chromosomal imbalance.
J R Korenberg, X N Chen, R Schipper, Z Sun, R Gonsky, S Gerwehr, N Carpenter, C Daumer, P Dignan, C Disteche. Proc Natl Acad Sci U S A 1994
518
14

Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.
M K McCormick, A Schinzel, M B Petersen, G Stetten, D J Driscoll, E S Cantu, L Tranebjaerg, M Mikkelsen, P C Watkins, S E Antonarakis. Genomics 1989
179
14

Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions.
K Gardiner, M Horisberger, J Kraus, U Tantravahi, J Korenberg, V Rao, S Reddy, D Patterson. EMBO J 1990
226
14

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies.
Daniela Ehling, Ingo Kennerknecht, Annelore Junge, Bettina Prager, Rita Exeler, Beate Behre, Juergen Horst, Thomas Schmitt-John, Oliver Bartsch, Jutta Wirth. Am J Med Genet A 2004
26
23

No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.
C Pangalos, D Théophile, P M Sinet, A Marks, D Stamboulieh-Abazis, Z Chettouh, M Prieur, C Verellen, M O Rethoré, J Lejeune. Am J Hum Genet 1992
40
12

Full monosomy 21: a clinically recognizable syndrome?
J P Fryns, F D'Hondt, P Goddeeris, H van den Berghe. Hum Genet 1977
48
12



Molecular mapping of twenty-four features of Down syndrome on chromosome 21.
J M Delabar, D Theophile, Z Rahmani, Z Chettouh, J L Blouin, M Prieur, B Noel, P M Sinet. Eur J Hum Genet 1993
299
9

Physical mapping of the holoprosencephaly critical region on chromosome 7q36.
F Gurrieri, B J Trask, G van den Engh, C M Krauss, A Schinzel, M J Pettenati, D Schindler, J Dietz-Band, G Vergnaud, S W Scherer. Nat Genet 1993
83
9

Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
199
9




Holoprosencephaly in infants of diabetic mothers.
M Barr, J W Hanson, K Currey, S Sharp, H Toriello, R D Schmickel, G N Wilson. J Pediatr 1983
159
9

Fetal t(5p;21q) misdiagnosed as monosomy 21: a plea for in situ hybridization studies.
P Gill, S Uhrich, C Disteche, E Cheng. Am J Med Genet 1994
18
22


Monosomy 21: a new case confirmed by in situ hybridization.
M C Pellissier, N Philip, M A Voelckel-Baeteman, M G Mattei, J F Mattei. Hum Genet 1987
34
11

Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies.
W Courtens, M B Petersen, J C Noël, J Flament-Durand, N Van Regemorter, D Delneste, P Cochaux, M R Verschraegen-Spae, N Van Roy, F Speleman. Am J Med Genet 1994
19
21

A familial interstitial deletion of the long arm of chromosome 21.
B Roland, D M Cox, D I Hoar, S B Fowlow, A S Robertson. Clin Genet 1990
26
15



Exon amplification: a strategy to isolate mammalian genes based on RNA splicing.
A J Buckler, D D Chang, S L Graw, J D Brook, D A Haber, P A Sharp, D E Housman. Proc Natl Acad Sci U S A 1991
466
9


What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
8

An integrated YAC-overlap and 'cosmid-pocket' map of the human chromosome 21.
D Nizetić, L Gellen, R M Hamvas, R Mott, A Grigoriev, R Vatcheva, G Zehetner, M L Yaspo, A Dutriaux, C Lopes. Hum Mol Genet 1994
89
7

A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.
R E Straub, T Lehner, Y Luo, J E Loth, W Shao, L Sharpe, J R Alexander, K Das, R Simon, R R Fieve. Nat Genet 1994
256
7

Cloning of a human homolog of the Drosophila minibrain/rat Dyrk gene from "the Down syndrome critical region" of chromosome 21.
N Shindoh, J Kudoh, H Maeda, A Yamaki, S Minoshima, Y Shimizu, N Shimizu. Biochem Biophys Res Commun 1996
97
7

The DNA sequence of human chromosome 21.
M Hattori, A Fujiyama, T D Taylor, H Watanabe, T Yada, H S Park, A Toyoda, K Ishii, Y Totoki, D K Choi,[...]. Nature 2000
765
7

Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
137
7


Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations.
E Rossi, F Piccini, M Zollino, G Neri, D Caselli, R Tenconi, C Castellan, R Carrozzo, C Danesino, O Zuffardi,[...]. J Med Genet 2001
106
7

Fetal holoprosencephaly: associated malformations and chromosomal defects.
S M Berry, C Gosden, R J Snijders, K H Nicolaides. Fetal Diagn Ther 1990
32
9


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.