A citation-based method for searching scientific literature

C J Epstein. Am J Hum Genet 1992
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


American Board of Medical Genetics restructuring: make an informed decision.
A Heimler, J Benkendorf, E Gettig, E Reich, S Schmerler, H Travers. Am J Hum Genet 1992
3
100


Genetic counseling.
. Am J Hum Genet 1975
110
25

Who should do genetic counseling, and under what circumstances?
C J Epstein. Birth Defects Orig Artic Ser 1973
8
25


Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency.
B Z Yang, J H Ding, T Dewese, D Roe, G He, J Wilkinson, D W Day, F Demaugre, D Rabier, M Brivet,[...]. Mol Genet Metab 1998
24
12


Forearm semi-ischemic exercise test in pediatric patients.
C Bruno, M Bado, C Minetti, G Cordone. J Child Neurol 1998
9
12


Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations.
E Verderio, P Cavadini, L Montermini, H Wang, E Lamantea, G Finocchiaro, S DiDonato, C Gellera, F Taroni. Hum Mol Genet 1995
73
12

Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis.
I Tein, J Christodoulou, E Donner, R R McInnes. J Pediatr 1994
17
12

Novel mutations associated with carnitine palmitoyltransferase II deficiency.
R T Taggart, D Smail, C Apolito, G D Vladutiu. Hum Mutat 1999
69
12

cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase.
G Finocchiaro, F Taroni, M Rocchi, A L Martin, I Colombo, G T Tarelli, S DiDonato. Proc Natl Acad Sci U S A 1991
122
12

Myoglobinuria associated with influenza A infection.
R A Minow, S Gorbach, B L Johnson, L Dornfeld. Ann Intern Med 1974
75
12


Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32.
C Gellera, E Verderio, G Floridia, G Finocchiaro, L Montermini, P Cavadini, O Zuffardi, F Taroni. Genomics 1994
46
12



Fatal carnitine palmitoyltransferase II deficiency in a newborn: new phenotypic features.
M R Pierce, G Pridjian, S Morrison, A S Pickoff. Clin Pediatr (Phila) 1999
19
12

Infantile form of carnitine palmitoyltransferase II deficiency in a girl with rapid fatal onset.
C Vianey-Saban, N Stremler, O Paut, T Buttin, P Divry, M T Zabot, J Camboulives, M Mathieu, B Mousson. J Inherit Metab Dis 1995
9
12


Carnitine palmitoyltransferase II deficiency: diagnosis by molecular analysis of blood.
P Kaufmann, M el-Schahawi, S DiMauro. Mol Cell Biochem 1997
27
12


Metabolic causes of myoglobinuria.
P Tonin, P Lewis, S Servidei, S DiMauro. Ann Neurol 1990
134
12

Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expression.
J P Bonnefont, F Taroni, P Cavadini, C Cepanec, M Brivet, J M Saudubray, J P Leroux, F Demaugre. Am J Hum Genet 1996
74
12


A novel mutation identified in carnitine palmitoyltransferase II deficiency.
B Z Yang, J H Ding, D Roe, T Dewese, D W Day, C R Roe. Mol Genet Metab 1998
26
12


Molecular characterization of inherited carnitine palmitoyltransferase II deficiency.
F Taroni, E Verderio, S Fiorucci, P Cavadini, G Finocchiaro, G Uziel, E Lamantea, C Gellera, S DiDonato. Proc Natl Acad Sci U S A 1992
124
12

Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneys.
K N North, C L Hoppel, U De Girolami, H P Kozakewich, M S Korson. J Pediatr 1995
63
12




[Study of somatic chromosomes from 9 mongoloid children].
J LEJEUNE, M GAUTIER, R TURPIN. C R Hebd Seances Acad Sci 1959
799
12

Hereditary dysplasia of bone with kyphoscoliosis, contractures, and abnormally shaped ears.
C J Epstein, C B Graham, W E Hodgkin, F Hecht, A G Motulsky. J Pediatr 1968
33
12

The center-satellite system for the wide-scale distribution of genetic counseling services.
C J Epstein, R P Erickson, B D Hall, M S Golbus. Am J Hum Genet 1975
18
12


Seven momentous years.
C J Epstein. Am J Hum Genet 1993
15
12

2010 Victor A. McKusick Leadership Award introduction and address.
Arno Motulsky, Charles J Epstein. Am J Hum Genet 2011
2
50




Performance indicators for assessing competencies of preventive medicine residents.
D S Lane, V Ross, M D Parkinson, D W Chen. Am J Prev Med 1995
18
12


The critical incident technique.
J C FLANAGAN. Psychol Bull 1954
12


Report of the 1989 Asilomar meeting on education in genetic counseling.
A P Walker, J A Scott, B B Biesecker, B Conover, W Blake, L Djurdjinovic. Am J Hum Genet 1990
36
12


An explication of the National Society of Genetic Counselors (NSGC) code of ethics.
Judith L Benkendorf, Nancy P Callanan, Rose Grobstein, Susan Schmerler, Kevin T FitzGerald. J Genet Couns 1992
26
12

The genetic associate: a career option in genetic counseling.
T R Mertens, J R Hendrix, K M Kenkel. J Hered 1986
5
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.