A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty.
D J Tomkins, A F Roux, J Waye, V C Freeman, D W Cox, D T Whelan. Eur J Hum Genet 1996
52
40

Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.
L M Brzustowicz, B A Allitto, D Matseoane, R Theve, L Michaud, S Chatkupt, E Sugarman, G K Penchaszadeh, L Suslak, M R Koenigsberger. Am J Hum Genet 1994
42
40

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
62
40


Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.
S E Antonarakis, J L Blouin, J Maher, D Avramopoulos, G Thomas, C C Talbot. Am J Hum Genet 1993
93
40

Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.
Dieter Kotzot, Gerd Utermann. Am J Med Genet A 2005
116
40

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination.
W P Robinson, B D Kuchinka, F Bernasconi, M B Petersen, A Schulze, K Brondum-Nielsen, S L Christian, D H Ledbetter, A A Schinzel, B Horsthemke,[...]. Hum Mol Genet 1998
89
20

The origin of numerical chromosome abnormalities.
P A Jacobs, T J Hassold. Adv Genet 1995
70
20

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.
I Henry, C Bonaiti-Pellié, V Chehensse, C Beldjord, C Schwartz, G Utermann, C Junien. Nature 1991
372
20

Uniparental maternal disomy 6 in a renal transplant patient.
E M van den Berg-Loonen, P Savelkoul, H van Hooff, P van Eede, A Riesewijk, J Geraedts. Hum Immunol 1996
32
20

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
20

A GNAS1 imprinting defect in pseudohypoparathyroidism type IB.
J Liu, D Litman, M J Rosenberg, S Yu, L G Biesecker, L S Weinstein. J Clin Invest 2000
192
20

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
20

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.
S L Sherman, M B Petersen, S B Freeman, J Hersey, D Pettay, L Taft, M Frantzen, M Mikkelsen, T J Hassold. Hum Mol Genet 1994
121
20



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
20


Maternal uniparental disomy of chromosome 13 in a phenotypically normal child.
H Slater, J H Shaw, G Dawson, A Bankier, S M Forrest. J Med Genet 1994
36
20

Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene.
Silvia Spena, Stefano Duga, Rosanna Asselta, Flora Peyvandi, Chularatana Mahasandana, Massimo Malcovati, Maria Luisa Tenchini. Eur J Hum Genet 2004
30
20

Segmental maternal heterodisomy of the proximal part of chromosome 15 in an infant with Prader-Willi syndrome.
Sergey Nazarenko, Elena Sazhenova, Alessandra Baumer, Albert Schinzel. Eur J Hum Genet 2004
10
20

Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.
A U López-Gutiérrez, L Riba, M L Ordoñez-Sánchez, S Ramírez-Jiménez, M Cerrillo-Hinojosa, M T Tusié-Luna. J Med Genet 1998
38
20

Maternal uniparental disomy for chromosome 14.
I K Temple, A Cockwell, T Hassold, D Pettay, P Jacobs. J Med Genet 1991
143
20

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.
D Kotzot, S Schmitt, F Bernasconi, W P Robinson, I W Lurie, H Ilyina, K Méhes, B C Hamel, B J Otten, M Hergersberg. Hum Mol Genet 1995
249
20

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
20

The neuronatin gene resides in a "micro-imprinted" domain on human chromosome 20q11.2.
H K Evans, A A Wylie, S K Murphy, R L Jirtle. Genomics 2001
71
20

Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.
François M Petit, Vincent Gajdos, Frédéric Parisot, Liliane Capel, Azzedine Aboura, Alain Lachaux, Gérard Tachdjian, Christian Poüs, Philippe Labrune. Eur J Hum Genet 2005
20
20

Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child.
B Röthlisberger, T Zerova, D Kotzot, T I Buzhievskaya, D Balmer, A Schinzel. J Med Genet 2001
26
20

Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients.
T Eggermann, S Mergenthaler, K Eggermann, A Albers, K Linnemann, C Fusch, M B Ranke, H A Wollmann. J Med Genet 2001
63
20

Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasia.
R P Spiro, S L Christian, D H Ledbetter, M I New, R C Wilson, N Roizen, R L Rosenfield. Pediatr Res 1999
28
20

First confirmed case with paternal uniparental disomy of chromosome 16.
J Kohlhase, B Janssen, K Weidenauer, K Harms, I Bartels. Am J Med Genet 2000
23
20

Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.
T R Welch, L S Beischel, E Choi, K Balakrishnan, N A Bishof. J Clin Invest 1990
64
20


Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia.
R Mant, J Williams, P Asherson, E Parfitt, P McGuffin, M J Owen. Am J Med Genet 1994
127
20

Uniparental paternal disomy in Angelman's syndrome.
S Malcolm, J Clayton-Smith, M Nichols, S Robb, T Webb, J A Armour, A J Jeffreys, M E Pembrey. Lancet 1991
262
20



Silver-Russell syndrome and cystic fibrosis associated with maternal uniparental disomy 7.
U Hehr, S Dörr, M Hagemann, I Hansmann, U Preiss, S Brömme. Am J Med Genet 2000
24
20

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Maria Eriksson, W Ted Brown, Leslie B Gordon, Michael W Glynn, Joel Singer, Laura Scott, Michael R Erdos, Christiane M Robbins, Tracy Y Moses, Peter Berglund,[...]. Nature 2003
20

Uniparental disomy of chromosome 2 resulting in lethal trifunctional protein deficiency due to homozygous alpha-subunit mutations.
Ute Spiekerkoetter, Angela Eeds, Zou Yue, Jonathan Haines, Arnold W Strauss, Marshall Summar. Hum Mutat 2002
28
20


Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
R D Nicholls, J H Knoll, M G Butler, S Karam, M Lalande. Nature 1989
660
20

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
20

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
56
20

Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
M Genuardi, C Tozzi, M G Pomponi, M L Stagni, M Della Monica, G Scarano, F Calvieri, L Torrisi, G Neri. Eur J Hum Genet 1999
23
20

Uniparental disomy in steroid 5alpha-reductase 2 deficiency.
B Chávez, E Valdez, F Vilchis. J Clin Endocrinol Metab 2000
37
20

Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities.
S Das, C M Lese, M Song, J L Jensen, L A Wells, B L Barnoski, J A Roseberry, J M Camacho, D H Ledbetter, R E Schnur. Am J Hum Genet 2000
27
20

Maternal uniparental disomy 22 has no impact on the phenotype.
A A Schinzel, S Basaran, F Bernasconi, B Karaman, M Yüksel-Apak, W P Robinson. Am J Hum Genet 1994
62
20

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.
N E Lamb, S B Freeman, A Savage-Austin, D Pettay, L Taft, J Hersey, Y Gu, J Shen, D Saker, K M May,[...]. Nat Genet 1996
281
20

Bloom syndrome and maternal uniparental disomy for chromosome 15.
T Woodage, M Prasad, J W Dixon, R E Selby, D R Romain, L M Columbano-Green, D Graham, P K Rogan, J R Seip, A Smith. Am J Hum Genet 1994
47
20


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.