A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.
Laurie J Ozelius, Geetha Senthil, Rachel Saunders-Pullman, Erin Ohmann, Amanda Deligtisch, Michele Tagliati, Ann L Hunt, Christine Klein, Brian Henick, Susan M Hailpern,[...]. N Engl J Med 2006
484
38

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
M H Polymeropoulos, C Lavedan, E Leroy, S E Ide, A Dehejia, A Dutra, B Pike, H Root, J Rubenstein, R Boyer,[...]. Science 1997
27

Association between early-onset Parkinson's disease and mutations in the parkin gene.
C B Lücking, A Dürr, V Bonifati, J Vaughan, G De Michele, T Gasser, B S Harhangi, G Meco, P Denèfle, N W Wood,[...]. N Engl J Med 2000
27

EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias.
H F Harbo, J Finsterer, J Baets, C Van Broeckhoven, S Di Donato, B Fontaine, P De Jonghe, A Lossos, T Lynch, C Mariotti,[...]. Eur J Neurol 2009
40
27

Comparing knowledge and attitudes towards genetic testing in Parkinson's disease in an American and Asian population.
Eng-King Tan, Jennie Lee, Christine Hunter, Lina Shinawi, S Fook-Chong, Joseph Jankovic. J Neurol Sci 2007
32
27

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.
R Krüger, W Kuhn, T Müller, D Woitalla, M Graeber, S Kösel, H Przuntek, J T Epplen, L Schöls, O Riess. Nat Genet 1998
22


Attitudes toward presymptomatic testing in Huntington disease.
C Mastromauro, R H Myers, B Berkman. Am J Med Genet 1987
127
22

alpha-Synuclein locus triplication causes Parkinson's disease.
A B Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, M Hulihan, T Peuralinna, A Dutra, R Nussbaum,[...]. Science 2003
22

PINK1 mutations are associated with sporadic early-onset parkinsonism.
Enza Maria Valente, Sergio Salvi, Tamara Ialongo, Roberta Marongiu, Antonio Emanuele Elia, Viviana Caputo, Luigi Romito, Alberto Albanese, Bruno Dallapiccola, Anna Rita Bentivoglio. Ann Neurol 2004
340
22

Genetic testing in Parkinson's disease.
Aideen McInerney-Leo, Donald W Hadley, Katrina Gwinn-Hardy, John Hardy. Mov Disord 2005
33
22

The genetics of Parkinson disease: Implications for neurological care.
Christine Klein, Michael G Schlossmacher. Nat Clin Pract Neurol 2006
123
22

Genetic testing and Parkinson disease: assessment of patient knowledge, attitudes, and interest.
Dana Clay Falcone, Elisabeth McCarty Wood, Sharon X Xie, Andrew Siderowf, Vivianna M Van Deerlin. J Genet Couns 2011
31
22

Attitudes, knowledge, and risk perceptions of women with breast and/or ovarian cancer considering testing for BRCA1 and BRCA2.
L G Bluman, B K Rimer, D A Berry, N Borstelmann, J D Iglehart, K Regan, J Schildkraut, E P Winer. J Clin Oncol 1999
105
16

The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.
Juan J Zarranz, Javier Alegre, Juan C Gómez-Esteban, Elena Lezcano, Raquel Ros, Israel Ampuero, Lídice Vidal, Janet Hoenicka, Olga Rodriguez, Begoña Atarés,[...]. Ann Neurol 2004
16

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease.
Ekaterina Rogaeva, Janel Johnson, Anthony E Lang, Cindy Gulick, Katrina Gwinn-Hardy, Toshitaka Kawarai, Christine Sato, Angharad Morgan, John Werner, Robert Nussbaum,[...]. Arch Neurol 2004
136
16

Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.
Matt Farrer, Jennifer Kachergus, Lysia Forno, Sarah Lincoln, Deng-Shun Wang, Mary Hulihan, Demetrius Maraganore, Katrina Gwinn-Hardy, Zbigniew Wszolek, Dennis Dickson,[...]. Ann Neurol 2004
502
16

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.
Vincenzo Bonifati, Patrizia Rizzu, Marijke J van Baren, Onno Schaap, Guido J Breedveld, Elmar Krieger, Marieke C J Dekker, Ferdinando Squitieri, Pablo Ibanez, Marijke Joosse,[...]. Science 2003
16

Attitudes of persons at risk for Huntington disease toward predictive testing.
S Kessler, T Field, L Worth, H Mosbarger. Am J Med Genet 1987
158
16


Hereditary early-onset Parkinson's disease caused by mutations in PINK1.
Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, Miratul M K Muqit, Kirsten Harvey, Suzana Gispert, Zeeshan Ali, Domenico Del Turco, Anna Rita Bentivoglio, Daniel G Healy,[...]. Science 2004
16

Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study.
Naheed L Khan, Enza Maria Valente, Anna Rita Bentivoglio, Nicholas W Wood, Alberto Albanese, David J Brooks, Paola Piccini. Ann Neurol 2002
159
16

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23.
M H Polymeropoulos, J J Higgins, L I Golbe, W G Johnson, S E Ide, G Di Iorio, G Sanges, E S Stenroos, L T Pho, A A Schaffer,[...]. Science 1996
515
16



LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs.
Suzanne Lesage, Alexandra Dürr, Meriem Tazir, Ebba Lohmann, Anne-Louise Leutenegger, Sabine Janin, Pierre Pollak, Alexis Brice. N Engl J Med 2006
392
16

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism.
Y Li, H Tomiyama, K Sato, Y Hatano, H Yoshino, M Atsumi, M Kitaguchi, S Sasaki, S Kawaguchi, H Miyajima,[...]. Neurology 2005
107
16

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.
Coro Paisán-Ruíz, Shushant Jain, E Whitney Evans, William P Gilks, Javier Simón, Marcel van der Brug, Adolfo López de Munain, Silvia Aparicio, Angel Martínez Gil, Naheed Khan,[...]. Neuron 2004
16

Genetic testing in Parkinson disease: promises and pitfalls.
Eng-King Tan, Joseph Jankovic. Arch Neurol 2006
46
16

Impact of recent genetic findings in Parkinson's disease.
Christine Klein, Katja Lohmann-Hedrich. Curr Opin Neurol 2007
69
16

A map of human genome variation from population-scale sequencing.
Gonçalo R Abecasis, David Altshuler, Adam Auton, Lisa D Brooks, Richard M Durbin, Richard A Gibbs, Matt E Hurles, Gil A McVean. Nature 2010
16

Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies.
Joseph R Mazzulli, You-Hai Xu, Ying Sun, Adam L Knight, Pamela J McLean, Guy A Caldwell, Ellen Sidransky, Gregory A Grabowski, Dimitri Krainc. Cell 2011
799
16

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
Alfredo Ramirez, André Heimbach, Jan Gründemann, Barbara Stiller, Dan Hampshire, L Pablo Cid, Ingrid Goebel, Ammar F Mubaidin, Abdul-Latif Wriekat, Jochen Roeper,[...]. Nat Genet 2006
772
16

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
E Sidransky, M A Nalls, J O Aasly, J Aharon-Peretz, G Annesi, E R Barbosa, A Bar-Shira, D Berg, J Bras, A Brice,[...]. N Engl J Med 2009
16

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.
R Hilker, C Klein, M Ghaemi, B Kis, T Strotmann, L J Ozelius, O Lenz, P Vieregge, K Herholz, W D Heiss,[...]. Ann Neurol 2001
187
11

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
T Kitada, S Asakawa, N Hattori, H Matsumine, Y Yamamura, S Minoshima, M Yokochi, Y Mizuno, N Shimizu. Nature 1998
11

Alpha-synuclein in Lewy bodies.
M G Spillantini, M L Schmidt, V M Lee, J Q Trojanowski, R Jakes, M Goedert. Nature 1997
11

How much phenotypic variation can be attributed to parkin genotype?
Ebba Lohmann, Magali Periquet, Vincenzo Bonifati, Nick W Wood, Giuseppe De Michele, Anne-Marie Bonnet, Valérie Fraix, Emmanuel Broussolle, Martin W I M Horstink, Marie Vidailhet,[...]. Ann Neurol 2003
219
11

Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors.
W C McKinnon, B J Baty, R L Bennett, M Magee, W A Neufeld-Kaiser, K F Peters, J C Sawyer, K A Schneider. JAMA 1997
77
11

Uptake of presymptomatic predictive testing for Huntington's disease.
D Craufurd, A Dodge, L Kerzin-Storrar, R Harris. Lancet 1989
180
11

PINK1 (PARK6) associated Parkinson disease in Ireland.
D G Healy, P M Abou-Sleiman, J M Gibson, O A Ross, S Jain, S Gandhi, D Gosal, M M K Muqit, N W Wood, T Lynch. Neurology 2004
76
11

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.
Karsten M Strauss, L Miguel Martins, Helene Plun-Favreau, Frank P Marx, Sabine Kautzmann, Daniela Berg, Thomas Gasser, Zbginiew Wszolek, Thomas Müller, Antje Bornemann,[...]. Hum Mol Genet 2005
387
11

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century.
Suzanne Lesage, Anne-Louise Leutenegger, Pablo Ibanez, Sabine Janin, Ebba Lohmann, Alexandra Dürr, Alexis Brice. Am J Hum Genet 2005
102
11

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew Farrer, Sarah Lincoln, Jennifer Kachergus, Mary Hulihan, Ryan J Uitti, Donald B Calne,[...]. Neuron 2004
11

Attitudes about genetics in underserved, culturally diverse populations.
Diana S Catz, Nancy S Green, Jonathan N Tobin, Michele A Lloyd-Puryear, Penny Kyler, Ann Umemoto, Jennifer Cernoch, Roxane Brown, Fredericka Wolman. Community Genet 2005
109
11

Attitudes, knowledge, risk perceptions and decision-making among women with breast and/or ovarian cancer considering testing for BRCA1 and BRCA2 and their spouses.
Leslie G Bluman, Barbara K Rimer, Katherine Regan Sterba, Julia Lancaster, Shelly Clark, Nancy Borstelmann, J Dirk Iglehart, Eric P Winer. Psychooncology 2003
20
11

alpha-Synuclein gene duplication is present in sporadic Parkinson disease.
T-B Ahn, S Y Kim, J Y Kim, S-S Park, D S Lee, H J Min, Y K Kim, S E Kim, J-M Kim, H-J Kim,[...]. Neurology 2008
162
11

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation.
N L Khan, C Scherfler, E Graham, K P Bhatia, N Quinn, A J Lees, D J Brooks, N W Wood, P Piccini. Neurology 2005
103
11

Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease.
S Goldwurm, M Zini, L Mariani, S Tesei, R Miceli, F Sironi, M Clementi, V Bonifati, G Pezzoli. Neurology 2007
94
11

Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.
Jung Mi Choi, Myoung Soo Woo, Hyeo-Il Ma, Suk Yun Kang, Young-Hee Sung, Seok Woo Yong, Sun Ju Chung, Joong-Seok Kim, Hae-won Shin, Chul Hyoung Lyoo,[...]. Neurogenetics 2008
71
11


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.