A citation-based method for searching scientific literature

P S Harper. J Med Genet 1993
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


A polymorphic DNA marker genetically linked to Huntington's disease.
J F Gusella, N S Wexler, P M Conneally, S L Naylor, M A Anderson, R E Tanzi, P C Watkins, K Ottina, M R Wallace, A Y Sakaguchi. Nature 1983
30

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease.
S E Andrew, Y P Goldberg, B Kremer, H Telenius, J Theilmann, S Adam, E Starr, F Squitieri, B Lin, M A Kalchman. Nat Genet 1993
785
30


Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuria.
V Romano, I Dianzani, A Ponzone, E Zammarchi, R Eisensmith, N Ceratto, P Bosco, A Indelicato. Prenat Diagn 1994
8
12







Non-invasive first trimester antenatal diagnosis.
N Morris, R Williamson. Br J Obstet Gynaecol 1992
23
10


Alternative splicing of the FMR1 gene in human fetal brain neurons.
T Huang, L Y Li, Y Shen, X B Qin, Z L Pang, G Y Wu. Am J Med Genet 1996
10
10

Detection of fetal cells in maternal blood.
S C Yeoh, I L Sargent, C W Redman, B P Wordsworth, S L Thein. Prenat Diagn 1991
50
10


Fetal nucleated cells in maternal peripheral blood: frequency and relationship to gestational age.
H Hamada, T Arinami, T Kubo, H Hamaguchi, H Iwasaki. Hum Genet 1993
188
10

Prediction of psychological functioning one year after the predictive test for Huntington's disease and impact of the test result on reproductive decision making.
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, J J Cassiman, T Cloostermans, K Demyttenaere, R Dom, J P Fryns, H Van den Berghe. J Med Genet 1996
103
10

The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.
R R Brinkman, M M Mezei, J Theilmann, E Almqvist, M R Hayden. Am J Hum Genet 1997
254
10

Dilemmas of anonymous predictive testing for Huntington disease: privacy vs. optimal care.
M M Burgess, S Adam, M Bloch, M R Hayden. Am J Med Genet 1997
16
10

Prenatal diagnosis for Huntington's disease: a molecular and psychological study.
A Spurdle, J Kromberg, J Rosendorff, T Jenkins. Prenat Diagn 1991
4
25

Huntington's disease confirmed by genetic testing in five African families.
E Silber, J Kromberg, J A Temlett, A Krause, D Saffer. Mov Disord 1998
15
10


A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.
B Kremer, P Goldberg, S E Andrew, J Theilmann, H Telenius, J Zeisler, F Squitieri, B Lin, A Bassett, E Almqvist. N Engl J Med 1994
416
10



Reduced penetrance of the Huntington's disease mutation.
S M McNeil, A Novelletto, J Srinidhi, G Barnes, I Kornbluth, M R Altherr, J J Wasmuth, J F Gusella, M E MacDonald, R H Myers. Hum Mol Genet 1997
86
10


Mutation size and age at onset in Huntington's disease.
D Craufurd, A Dodge. J Med Genet 1993
36
10


Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.
D C Rubinsztein, J Leggo, R Coles, E Almqvist, V Biancalana, J J Cassiman, K Chotai, M Connarty, D Crauford, A Curtis,[...]. Am J Hum Genet 1996
339
10

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.
B Kremer, E Almqvist, J Theilmann, N Spence, H Telenius, Y P Goldberg, M R Hayden. Am J Hum Genet 1995
110
10


Huntington disease: genetics and epidemiology.
P M Conneally. Am J Hum Genet 1984
170
10

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.
I M van der Steenstraten, A Tibben, R A Roos, J J van de Kamp, M F Niermeijer. Am J Hum Genet 1994
103
10

The effects of MAOA genotype, childhood trauma, and sex on trait and state-dependent aggression.
Floor E A Verhoeven, Linda Booij, Anne-Wil Kruijt, Hilâl Cerit, Niki Antypa, Willem Does. Brain Behav 2012
44
10

Serotonin transporter genetic variation and the response of the human amygdala.
Ahmad R Hariri, Venkata S Mattay, Alessandro Tessitore, Bhaskar Kolachana, Francesco Fera, David Goldman, Michael F Egan, Daniel R Weinberger. Science 2002
10

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.
M G Spillantini, J R Murrell, M Goedert, M R Farlow, A Klug, B Ghetti. Proc Natl Acad Sci U S A 1998
10

Interaction between MAO-A genotype and maltreatment in the risk for conduct disorder: failure to confirm in adolescent patients.
Susan E Young, Andrew Smolen, John K Hewitt, Brett C Haberstick, Michael C Stallings, Robin P Corley, Thomas J Crowley. Am J Psychiatry 2006
87
10

Childhood maltreatment, subsequent antisocial behavior, and the role of monoamine oxidase A genotype.
David Huizinga, Brett C Haberstick, Andrew Smolen, Scott Menard, Susan E Young, Robin P Corley, Michael C Stallings, Jennifer Grotpeter, John K Hewitt. Biol Psychiatry 2006
101
10

Full-length cDNA cloning and distribution of human dopamine D4 receptor.
M Matsumoto, K Hidaka, S Tada, Y Tasaki, T Yamaguchi. Brain Res Mol Brain Res 1995
133
10

Meta-analysis of genetic association studies on bipolar disorder.
Fayaz Seifuddin, Pamela Belmonte Mahon, Jennifer Judy, Mehdi Pirooznia, Dubravka Jancic, Jacob Taylor, Fernando S Goes, James B Potash, Peter P Zandi. Am J Med Genet B Neuropsychiatr Genet 2012
46
10


Allelic variation of human serotonin transporter gene expression.
A Heils, A Teufel, S Petri, G Stöber, P Riederer, D Bengel, K P Lesch. J Neurochem 1996
10

Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder.
J Deckert, M Catalano, Y V Syagailo, M Bosi, O Okladnova, D Di Bella, M M Nöthen, P Maffei, P Franke, J Fritze,[...]. Hum Mol Genet 1999
453
10

COMT158 polymorphism and hostility.
Jan Volavka, James L Kennedy, Xingqun Ni, Pal Czobor, Karen Nolan, Brian Sheitman, Jean-Pierre Lindenmayer, Leslie Citrome, Joseph McEvoy, Jeffrey A Lieberman. Am J Med Genet B Neuropsychiatr Genet 2004
25
10

Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
J C Janssen, J A Beck, T A Campbell, A Dickinson, N C Fox, R J Harvey, H Houlden, M N Rossor, J Collinge. Neurology 2003
203
10

New functional single nucleotide polymorphism (Ala72Ser) in the COMT gene is associated with aggressive behavior in male schizophrenia.
Jin Pyo Hong, Joongsun S Lee, Seockhoon Chung, Jaeyeul Jung, Hanik K Yoo, Sung Man Chang, Chang Yoon Kim. Am J Med Genet B Neuropsychiatr Genet 2008
23
10

"We are also normal humans, you know?" Views and attitudes of juvenile delinquents on antisocial behavior, neurobiology and prevention.
Dorothee Horstkötter, Ron Berghmans, Corine de Ruiter, Anja Krumeich, Guido de Wert. Int J Law Psychiatry 2012
5
20


5-HTTLPR genotype and anxiety-related personality traits: a meta-analysis and new data.
Marcus R Munafò, Nelson B Freimer, Whitney Ng, Roel Ophoff, Juha Veijola, Jouko Miettunen, Marjo-Riitta Järvelin, Anja Taanila, Jonathan Flint. Am J Med Genet B Neuropsychiatr Genet 2009
167
10


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.