A citation-based method for searching scientific literature

M Ehrlich, F Tsien, D Herrera, V Blackman, J Roggenbuck, C M Tuck-Muller. J Med Genet 2001
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


DNA demethylation and pericentromeric rearrangements of chromosome 1.
W Ji, R Hernandez, X Y Zhang, G Z Qu, A Frady, M Varela, M Ehrlich. Mutat Res 1997
136
57

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes.
M Ehrlich, K L Buchanan, F Tsien, G Jiang, B Sun, W Uicker, C M Weemaes, D Smeets, K Sperling, B H Belohradsky,[...]. Hum Mol Genet 2001
91
57

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene.
G L Xu, T H Bestor, D Bourc'his, C L Hsieh, N Tommerup, M Bugge, M Hulten, X Qu, J J Russo, E Viegas-Péquignot. Nature 1999
824
57

Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9, and 16.
N J Carpenter, A Filipovich, R M Blaese, T L Carey, A I Berkel. J Pediatr 1988
38
42

Genetic variation in ICF syndrome: evidence for genetic heterogeneity.
C Wijmenga, R S Hansen, G Gimelli, E J Björck, E G Davies, D Valentine, B H Belohradsky, J J van Dongen, D F Smeets, L P van den Heuvel,[...]. Hum Mutat 2000
71
42

Amount and distribution of 5-methylcytosine in human DNA from different types of tissues of cells.
M Ehrlich, M A Gama-Sosa, L H Huang, R M Midgett, K C Kuo, R A McCune, C Gehrke. Nucleic Acids Res 1982
645
42


Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency.
L Tiepolo, P Maraschio, G Gimelli, C Cuoco, G F Gargani, C Romano. Hum Genet 1979
89
42


An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
M Jeanpierre, C Turleau, A Aurias, M Prieur, F Ledeist, A Fischer, E Viegas-Pequignot. Hum Mol Genet 1993
215
42

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
C M Tuck-Muller, A Narayan, F Tsien, D F Smeets, J Sawyer, E S Fiala, O S Sohn, M Ehrlich. Cytogenet Cell Genet 2000
171
42

Hypomethylation of pericentromeric DNA in breast adenocarcinomas.
A Narayan, W Ji, X Y Zhang, A Marrogi, J R Graff, S B Baylin, M Ehrlich. Int J Cancer 1998
182
42

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome.
R S Hansen, C Wijmenga, P Luo, A M Stanek, T K Canfield, C M Weemaes, S M Gartler. Proc Natl Acad Sci U S A 1999
519
42




Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.
T Kondo, M P Bobek, R Kuick, B Lamb, X Zhu, A Narayan, D Bourc'his, E Viegas-Péquignot, M Ehrlich, S M Hanash. Hum Mol Genet 2000
130
42

ICF syndrome: a new case and review of the literature.
D F Smeets, U Moog, C M Weemaes, G Vaes-Peeters, G F Merkx, J P Niehof, G Hamers. Hum Genet 1994
88
28

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
C Turleau, M O Cabanis, D Girault, F Ledeist, R Mettey, H Puissant, M Prieur, J de Grouchy. Am J Med Genet 1989
46
28

Spontaneous chromosome fragility in chorionic villus cells.
L Míguez, C Fuster, M M Pérez, R Miró, J Egozcue. Early Hum Dev 1991
21
28

The ICF syndrome: new case and update.
T J De Ravel, E Deckers, P L Alliet, P Petit, J P Fryns. Genet Couns 2001
11
28

DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor.
S Schuffenhauer, O Bartsch, M Stumm, T Buchholz, T Petropoulou, S Kraft, B Belohradsky, G K Hinkel, T Meitinger, R D Wegner. Hum Genet 1995
49
28

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
P Miniou, M Jeanpierre, V Blanquet, V Sibella, D Bonneau, C Herbelin, A Fischer, A Niveleau, E Viegas-Péquignot. Hum Mol Genet 1994
112
28



Human satellites 2 and 3.
M Jeanpierre. Ann Genet 1994
38
28

Frequent hypomethylation in Wilms tumors of pericentromeric DNA in chromosomes 1 and 16.
G Z Qu, P E Grundy, A Narayan, M Ehrlich. Cancer Genet Cytogenet 1999
109
28


Epigenetic reprogramming in mouse primordial germ cells.
Petra Hajkova, Sylvia Erhardt, Natasha Lane, Thomas Haaf, Osman El-Maarri, Wolf Reik, Jörn Walter, M Azim Surani. Mech Dev 2002
795
28

The 5-methylcytosine content of DNA from human tumors.
M A Gama-Sosa, V A Slagel, R W Trewyn, R Oxenhandler, K C Kuo, C W Gehrke, M Ehrlich. Nucleic Acids Res 1983
625
28


Role for DNA methylation in genomic imprinting.
E Li, C Beard, R Jaenisch. Nature 1993
28


Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation.
L Jackson-Grusby, C Beard, R Possemato, M Tudor, D Fambrough, G Csankovszki, J Dausman, P Lee, C Wilson, E Lander,[...]. Nat Genet 2001
508
28


Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability.
A H Peters, D O'Carroll, H Scherthan, K Mechtler, S Sauer, C Schöfer, K Weipoltshammer, M Pagani, M Lachner, A Kohlmaier,[...]. Cell 2001
28

Sp1 elements protect a CpG island from de novo methylation.
M Brandeis, D Frank, I Keshet, Z Siegfried, M Mendelsohn, A Nemes, V Temper, A Razin, H Cedar. Nature 1994
613
28


The fundamental role of epigenetic events in cancer.
Peter A Jones, Stephen B Baylin. Nat Rev Genet 2002
28

Hypomethylation and hypermethylation of DNA in Wilms tumors.
Melanie Ehrlich, Guanchao Jiang, Emerich Fiala, Jeffrey S Dome, Mimi C Yu, Tiffany I Long, Byungwoo Youn, Ock-Soon Sohn, Martin Widschwendter, Gail E Tomlinson,[...]. Oncogene 2002
138
28

Overexpression of a splice variant of DNA methyltransferase 3b, DNMT3b4, associated with DNA hypomethylation on pericentromeric satellite regions during human hepatocarcinogenesis.
Yoshimasa Saito, Yae Kanai, Michiie Sakamoto, Hidetsugu Saito, Hiromasa Ishii, Setsuo Hirohashi. Proc Natl Acad Sci U S A 2002
161
28


Hypomethylation of ras oncogenes in primary human cancers.
A P Feinberg, B Vogelstein. Biochem Biophys Res Commun 1983
406
28


DNA hypomethylation and ovarian cancer biology.
Martin Widschwendter, Guanchao Jiang, Christian Woods, Hannes M Müller, Heidi Fiegl, Georg Goebel, Christian Marth, Elisabeth Müller-Holzner, Alain G Zeimet, Peter W Laird,[...]. Cancer Res 2004
165
28

Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
F Tsien, B Sun, N E Hopkins, V Vedanarayanan, D Figlewicz, S Winokur, M Ehrlich. Mol Genet Metab 2001
28
28

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.
Y L Jiang, M Rigolet, D Bourc'his, F Nigon, I Bokesoy, J P Fryns, M Hultén, P Jonveaux, P Maraschio, A Mégarbané,[...]. Hum Mutat 2005
74
28





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.