A citation-based method for searching scientific literature

A Cooke, J Tolmie, W Darlington, E Boyd, R Thomson, M A Ferguson-Smith. J Med Genet 1987
Times Cited: 34







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



Times Cited
  Times     Co-cited
Similarity


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
61

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
80

16q21 is critical for 16q deletion syndrome.
K Naritomi, N Shiroma, Y Izumikawa, K Sameshima, S Ohdo, K Hirayama. Clin Genet 1988
26
73

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
61

Interstitial 16q deletion with typical dysmorphic syndrome.
J P Fryns, W Proesmans, G Van Hoey, H Van den Berghe. Ann Genet 1981
30
63


Interstitial deletion and ring chromosome derived from 16q.
C M Krauss, D Caldwell, L Atkins. J Med Genet 1987
32
56

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
65

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
60



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
53

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
44

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
65



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
32

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
32

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







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
27

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994
27
33


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
26

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
26

Townes-Brocks syndrome in two mentally retarded youngsters.
T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991
31
29


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
26

STAT6: its role in interleukin 4-mediated biological functions.
K Takeda, T Kishimoto, S Akira. J Mol Med (Berl) 1997
96
26


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
170
26


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
26

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
322
26

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
45

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
26

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
26

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
26

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
26

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
26


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
26

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
36

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
37

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
26


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.