A citation-based method for searching scientific literature

B Röthlisberger, T Zerova, D Kotzot, T I Buzhievskaya, D Balmer, A Schinzel. J Med Genet 2001
Times Cited: 26







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



Times Cited
  Times     Co-cited
Similarity



Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy.
B M Anderlid, S Sahlén, J Schoumans, E Holmberg, I Ahsgren, G Mortier, F Speleman, E Blennow. Am J Med Genet 2001
62
38




Prenatal identification of de novo marker chromosomes using micro-FISH approach.
J Xu, C T Fong, E Cedrone, J Sullivan, N Wang. Clin Genet 1998
16
43

Origins of accessory small ring marker chromosomes derived from chromosome 1.
D F Callen, H Eyre, Y Y Fang, X Y Guan, A Veleba, N J Martin, J McGill, E A Haan. J Med Genet 1999
30
26

FISH characterization of a supernumerary r(1)(::cen-->q22::q22-->sq21::) chromosome associated with multiple anomalies and bilateral cataracts.
P Finelli, P Cavalli, D Giardino, G Gottardi, F Natacci, S Savasta, L Larizza. Am J Med Genet 2001
13
53

A search for uniparental disomy in carriers of supernumerary marker chromosomes.
R S James, I K Temple, N R Dennis, J A Crolla. Eur J Hum Genet 1995
62
23


FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes.
D Giardino, D Bettio, G Gottardi, N Rizzi, M Pierluigi, C Perfumo, A Calì, F Dagna Bricarelli, L Larizza. Am J Med Genet 1999
15
40

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
H Chen, C M Tuck-Muller, D A Batista, W Wertelecki. Am J Med Genet 1995
21
28

Mosaic trisomy of a small r(1) with an abnormal phenotype.
A J Dawson, D Konkin, D Riordan, A E Chudley. Am J Med Genet 2001
9
66

Maternal uniparental disomy of chromosome 1 with no apparent phenotypic effects.
L L Field, R Tobias, W P Robinson, R Paisey, S Bain. Am J Hum Genet 1998
45
23

Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1.
R Dufourcq-Lagelouse, N Lambert, M Duval, G Viot, E Vilmer, A Fischer, M Prieur, G de Saint Basile. Eur J Hum Genet 1999
49
23

Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis.
B D Gelb, J P Willner, T M Dunn, N B Kardon, A Verloes, J Poncin, R J Desnick. Am J Hum Genet 1998
57
23

Small supernumerary marker chromosomes (sSMC) in humans.
T Liehr, U Claussen, H Starke. Cytogenet Genome Res 2004
207
23

Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotype.
F Von Eggeling, C Hoppe, U Bartz, H Starke, G Houge, U Claussen, G Ernst, D Kotzot, T Liehr. J Med Genet 2002
14
35

Maternal UPD 20 in a hyperactive child with severe growth retardation.
I Chudoba, Y Franke, G Senger, G Sauerbrei, S Demuth, V Beensen, A Neumann, I Hansmann, U Claussen. Eur J Hum Genet 1999
63
19


Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
W P Robinson, J Wagstaff, F Bernasconi, C Baccichetti, L Artifoni, E Franzoni, L Suslak, L Y Shih, H Aviv, A A Schinzel. J Med Genet 1993
109
19

Forty four probands with an additional "marker" chromosome.
K E Buckton, G Spowart, M S Newton, H J Evans. Hum Genet 1985
219
19

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization.
R Plattner, N A Heerema, P N Howard-Peebles, J H Miles, S Soukup, C G Palmer. Hum Genet 1993
77
19

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.
D F Callen, H J Eyre, M L Ringenbergs, C J Freemantle, P Woodroffe, E A Haan. Am J Hum Genet 1991
141
19

Supernumerary chromosome marker (1) in a developmentally delayed child.
N Lanphear, A Lamb, S Oppenheimer, S Soukup. Am J Med Genet 1995
16
31

Characterization of a supernumerary ring chromosome 1 mosaicism in two cell systems by molecular cytogenetic techniques and review of the literature.
Holger Tönnies, Luitgard M Neumann, Berthild Grüneberg, Heidemarie Neitzel. Am J Med Genet A 2003
10
50

Simultaneous occurrence of two supernumerary autosomal ring chromosomes r(1) and r(16) in twins.
A L Shanske, P Dowling, R Schmidt, B J White, B Russell, A Bogdanow, R W Marion. J Med Genet 1999
14
35

Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis.
M M Li, P N Howard-Peebles, L D Killos, L Fallon, E Listgarten, W S Stanley. Prenat Diagn 2000
26
19




Uniparental isodisomy resulting from 46,XX,i(1p),i(1q) in a woman with short stature, ptosis, micro/retrognathia, myopathy, deafness, and sterility.
H Chen, R Young, X Mu, K Nandi, S Miao, L Prouty, S Ursin, J Gonzalez, K Yanamandra. Am J Med Genet 1999
16
31

Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively.
Debra A Thompson, Christina L McHenry, Yun Li, Julia E Richards, Mohammad I Othman, Eberhard Schwinger, Douglas Vollrath, Samuel G Jacobson, Andreas Gal. Am J Hum Genet 2002
94
19

Rare etiology of autosomal recessive disease in a child with noncarrier parents.
R V Lebo, L R Shapiro, E Y Fenerci, J M Hoover, J L Chuang, D T Chuang, D F Kronn. Am J Hum Genet 2000
21
23

Mutation report: complete paternal uniparental isodisomy of chromosome 1: a novel mechanism for Herlitz junctional epidermolysis bullosa.
Y Takizawa, L Pulkkinen, S C Chao, H Nakajima, Y Nakano, H Shimizu, J Uitto. J Invest Dermatol 2000
35
19

Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa.
H Fassihi, V Wessagowit, G H S Ashton, C Moss, R Ward, J Denyer, J E Mellerio, J A McGrath. Clin Exp Dermatol 2005
20
25



Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
B Huang, J A Crolla, S L Christian, M E Wolf-Ledbetter, M E Macha, P N Papenhausen, D H Ledbetter. Hum Genet 1997
93
15


Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.
D F Callen, M L Ringenbergs, J C Fowler, C J Freemantle, E A Haan. J Med Genet 1990
75
15

Clinical applications of comparative genomic hybridization.
B Levy, T M Dunn, S Kaffe, N Kardon, K Hirschhorn. Genet Med 1998
52
15



A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).
A Nietzel, M Rocchi, H Starke, A Heller, W Fiedler, I Wlodarska, I F Loncarevic, V Beensen, U Claussen, T Liehr. Hum Genet 2001
115
15

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Heike Starke, Angela Nietzel, Anja Weise, Anita Heller, Kristin Mrasek, Britta Belitz, Christine Kelbova, Marianne Volleth, Beate Albrecht, Beate Mitulla,[...]. Hum Genet 2003
133
15

Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1.
O Miyoshi, R Yabe, K Wakui, Y Fukushima, S Koizumi, M Uchikawa, T Kajii, C Numakura, S Takahashi, K Hayasaka,[...]. Am J Med Genet 2001
8
50


Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism.
C Jones, C Booth, D Rita, L Jazmines, R Spiro, B McCulloch, C McCaskill, L G Shaffer. Prenat Diagn 1995
25
12

Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effect.
C Mignon, P Malzac, A Moncla, D Depetris, N Roeckel, M F Croquette, M G Mattei. Eur J Hum Genet 1996
61
11


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.