A citation-based method for searching scientific literature

S Edelhoff, B Maier, U Trautmann, R A Pfeiffer. Ann Genet 1991
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


16q21 is critical for 16q deletion syndrome.
K Naritomi, N Shiroma, Y Izumikawa, K Sameshima, S Ohdo, K Hirayama. Clin Genet 1988
26
84

Deletion of 16q with prolonged survival and unusual radiographic manifestations.
A C Casamassima, R M Klein, P L Wilmot, P Brenholz, L R Shapiro. Am J Med Genet 1990
26
84


Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis.
A Cooke, J Tolmie, W Darlington, E Boyd, R Thomson, M A Ferguson-Smith. J Med Genet 1987
34
84

Interstitial deletion of chromosome 16q: 16q22 is critical for 16q- syndrome.
M Fujiwara, T Yoshimoto, Y Morita, M Kamada. Am J Med Genet 1992
28
84


Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters.
J J Hoo, R B Lowry, C C Lin, R H Haslam. Clin Genet 1985
31
78

Interstitial deletion for a region in the long arm of chromosome 16.
C C Lin, R B Lowry, F F Snyder. Hum Genet 1983
34
78

Interstitial deletion and ring chromosome derived from 16q.
C M Krauss, D Caldwell, L Atkins. J Med Genet 1987
32
73

Interstitial 16q deletion with typical dysmorphic syndrome.
J P Fryns, W Proesmans, G Van Hoey, H Van den Berghe. Ann Genet 1981
30
73

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
D F Callen, H Eyre, S Lane, Y Shen, I Hansmann, N Spinner, E Zackai, D McDonald-McGinn, S Schuffenhauer, J Wauters. J Med Genet 1993
42
68

Monosomy 16q: a distinct syndrome. Apropos of a de novo del(16) (q2100q2300).
H Rivera, E Vargas-Moyeda, M Möller, A Torres-Lamas, J M Cantú. Clin Genet 1985
25
68

De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boy.
S Schuffenhauer, D F Callen, H Seidel, Y Shen, G Lederer, J Murken. Clin Genet 1992
20
68

Partial monosomy of the long arm of chromosome 16: a distinct clinical entity?
J P Fryns, J Bande-Knops, H Van Den Berghe. Hum Genet 1979
28
57

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.
N P Carter, M A Ferguson-Smith, M T Perryman, H Telenius, A H Pelmear, M A Leversha, M T Glancy, S L Wood, K Cook, H M Dyson. J Med Genet 1992
173
57

Multiple critical smallest region of overlap in monosomy 16Q syndrome?
M Doco-Fenzy, J F Elchardus, G Brami, B Digeon, N Gruson, J J Adnet. Genet Couns 1994
13
84



A comprehensive genetic map of the human genome based on 5,264 microsatellites.
C Dib, S Fauré, C Fizames, D Samson, N Drouot, A Vignal, P Millasseau, S Marc, J Hazan, E Seboun,[...]. Nature 1996
52





Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population.
E Trabetti, V Cusin, G Malerba, L C Martinati, A Casartelli, A L Boner, P F Pignatti. J Med Genet 1998
33
47

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994
27
47



Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene.
B Burwinkel, L Amat, R G Gray, N Matsuo, K Muroya, K Narisawa, R J Sokol, M A Vilaseca, M W Kilimann. Hum Genet 1998
46
47

Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
M H Little, K A Williamson, M Mannens, A Kelsey, C Gosden, N D Hastie, V van Heyningen. Hum Mol Genet 1993
127
47

Townes-Brocks syndrome in two mentally retarded youngsters.
T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991
31
47


p53 abnormalities in B-cell prolymphocytic leukemia.
D Lens, P J De Schouwer, R A Hamoudi, M Abdul-Rauf, N Farahat, E Matutes, T Crook, M J Dyer, D Catovsky. Blood 1997
77
47

STAT6: its role in interleukin 4-mediated biological functions.
K Takeda, T Kishimoto, S Akira. J Mol Med (Berl) 1997
96
47


Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters.
U Suter, G J Snipes, R Schoener-Scott, A A Welcher, S Pareek, J R Lupski, R A Murphy, E M Shooter, P I Patel. J Biol Chem 1994
171
47


Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.
B B Roa, C A Garcia, U Suter, D A Kulpa, C A Wise, J Mueller, A A Welcher, G J Snipes, E M Shooter, P I Patel,[...]. N Engl J Med 1993
327
47

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism.
E M Rinchik, S J Bultman, B Horsthemke, S T Lee, K M Strunk, R A Spritz, K M Avidano, M T Jong, R D Nicholls. Nature 1993
323
47

Phosphorylase b kinase deficiency glycogenosis with cirrhosis of the liver.
A F Kagalwalla, Y A Kagalwalla, S al Ajaji, W Gorka, M A Ali. J Pediatr 1995
20
47

Control of inflammation, cytokine expression, and germinal center formation by BCL-6.
A L Dent, A L Shaffer, X Yu, D Allman, L M Staudt. Science 1997
738
47

Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.
A K Ryan, K Bartlett, P Clayton, S Eaton, L Mills, D Donnai, R M Winter, J Burn. J Med Genet 1998
173
47

Essential role of Stat6 in IL-4 signalling.
K Takeda, T Tanaka, W Shi, M Matsumoto, M Minami, S Kashiwamura, K Nakanishi, N Yoshida, T Kishimoto, S Akira. Nature 1996
47

Molecular and clinical study of 61 Angelman syndrome patients.
S Saitoh, N Harada, Y Jinno, K Hashimoto, K Imaizumi, Y Kuroki, Y Fukushima, T Sugimoto, M Renedo, J Wagstaff. Am J Med Genet 1994
72
47

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR.
A Martínez-Mir, E Paloma, R Allikmets, C Ayuso, T del Rio, M Dean, L Vilageliu, R Gonzàlez-Duarte, S Balcells. Nat Genet 1998
328
47


DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
J R Lupski, R M de Oca-Luna, S Slaugenhaupt, L Pentao, V Guzzetta, B J Trask, O Saucedo-Cardenas, D F Barker, J M Killian, C A Garcia,[...]. Cell 1991
47

Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
U Finckh, S Xu, G Kumaramanickavel, M Schürmann, J K Mukkadan, S T Fernandez, S John, J L Weber, M J Denton, A Gal. Genomics 1998
25
47

Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB).
I E van den Berg, E A van Beurden, J B de Klerk, O P van Diggelen, H E Malingré, M M Boer, R Berger. Am J Hum Genet 1997
24
47

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.
J Kohlhase, A Wischermann, H Reichenbach, U Froster, W Engel. Nat Genet 1998
330
47

A genome-wide search for linkage to asthma. German Asthma Genetics Group.
M Wjst, G Fischer, T Immervoll, M Jung, K Saar, F Rueschendorf, A Reis, M Ulbrecht, M Gomolka, E H Weiss,[...]. Genomics 1999
289
47


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.