A citation-based method for searching scientific literature

T H Wassink, J Piven, S R Patil. Psychiatr Genet 2001
Times Cited: 98







List of co-cited articles
1042 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Autism as a strongly genetic disorder: evidence from a British twin study.
A Bailey, A Le Couteur, I Gottesman, P Bolton, E Simonoff, E Yuzda, M Rutter. Psychol Med 1995
27

A genomic screen of autism: evidence for a multilocus etiology.
N Risch, D Spiker, L Lotspeich, N Nouri, D Hinds, J Hallmayer, L Kalaydjieva, P McCague, S Dimiceli, T Pitts,[...]. Am J Hum Genet 1999
507
25



A genomewide screen for autism susceptibility loci.
J Liu, D R Nyholt, P Magnussen, E Parano, P Pavone, D Geschwind, C Lord, P Iversen, J Hoh, J Ott,[...]. Am J Hum Genet 2001
239
21

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.
A Philippe, M Martinez, M Guilloud-Bataille, C Gillberg, M Råstam, E Sponheim, M Coleman, M Zappella, H Aschauer, L Van Maldergem,[...]. Hum Mol Genet 1999
379
21

Chromosomal disorders and autism.
C Gillberg. J Autism Dev Disord 1998
147
21

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.
J D Buxbaum, J M Silverman, C J Smith, M Kilifarski, J Reichert, E Hollander, B A Lawlor, M Fitzgerald, D A Greenberg, K L Davis. Am J Hum Genet 2001
252
20



The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.
C Lord, S Risi, L Lambrecht, E H Cook, B L Leventhal, P C DiLavore, A Pickles, M Rutter. J Autism Dev Disord 2000
18

An autosomal genomic screen for autism. Collaborative linkage study of autism.
S Barrett, J C Beck, R Bernier, E Bisson, T A Braun, T L Casavant, D Childress, S E Folstein, M Garcia, M B Gardiner,[...]. Am J Med Genet 1999
279
17

Genetics of autism: complex aetiology for a heterogeneous disorder.
S E Folstein, B Rosen-Sheidley. Nat Rev Genet 2001
507
17

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
17


Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.
E H Cook, V Lindgren, B L Leventhal, R Courchesne, A Lincoln, C Shulman, C Lord, E Courchesne. Am J Hum Genet 1997
474
16


A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden.
S Steffenburg, C Gillberg, L Hellgren, L Andersson, I C Gillberg, G Jakobsson, M Bohman. J Child Psychol Psychiatry 1989
543
14

Autism and maternally derived aberrations of chromosome 15q.
R J Schroer, M C Phelan, R C Michaelis, E C Crawford, S A Skinner, M Cuccaro, R J Simensen, J Bishop, C Skinner, D Fender,[...]. Am J Med Genet 1998
277
14

Genomic screen and follow-up analysis for autistic disorder.
Yujun Shao, Chantelle M Wolpert, Kimberly L Raiford, Marisa M Menold, Shannon L Donnelly, Sarah A Ravan, Meredyth P Bass, Cate McClain, Lennart von Wendt, Jeffery M Vance,[...]. Am J Med Genet 2002
180
14

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.
E H Cook, R Y Courchesne, N J Cox, C Lord, D Gonen, S J Guter, A Lincoln, K Nix, R Haas, B L Leventhal,[...]. Am J Hum Genet 1998
267
14

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.
Mari Auranen, Raija Vanhala, Teppo Varilo, Kristin Ayers, Elli Kempas, Tero Ylisaukko-Oja, Janet S Sinsheimer, Leena Peltonen, Irma Järvelä. Am J Hum Genet 2002
162
14

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.
Walter E Kaufmann, Ranon Cortell, Alice S M Kau, Irena Bukelis, Elaine Tierney, Robert M Gray, Christiane Cox, George T Capone, Pia Stanard. Am J Med Genet A 2004
284
14

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
14

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
14

Chromosomal abnormalities in a series of children with autistic disorder.
M M Konstantareas, S Homatidis. J Autism Dev Disord 1999
67
19


Value of a clinical morphology examination in autism.
J H Miles, R E Hillman. Am J Med Genet 2000
127
12

Infantile autism: a genetic study of 21 twin pairs.
S Folstein, M Rutter. J Child Psychol Psychiatry 1977
778
12

A case-control family history study of autism.
P Bolton, H Macdonald, A Pickles, P Rios, S Goode, M Crowson, A Bailey, M Rutter. J Child Psychol Psychiatry 1994
666
12


Molecular and cytogenetic analyses of autism in Taiwan.
S Y Li, Y C Chen, T J Lai, C Y Hsu, Y C Wang. Hum Genet 1993
32
34

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.
Frédéric Laumonnier, Frédérique Bonnet-Brilhault, Marie Gomot, Romuald Blanc, Albert David, Marie-Pierre Moizard, Martine Raynaud, Nathalie Ronce, Eric Lemonnier, Patrick Calvas,[...]. Am J Hum Genet 2004
526
11

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.
M-L Jacquemont, D Sanlaville, R Redon, O Raoul, V Cormier-Daire, S Lyonnet, J Amiel, M Le Merrer, D Heron, M-C de Blois,[...]. J Med Genet 2006
208
11

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Peter Szatmari, Andrew D Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiao-Qing Liu, John B Vincent, Jennifer L Skaug, Ann P Thompson, Lili Senman,[...]. Nat Genet 2007
969
11

Associated medical disorders and disabilities in children with autistic disorder: a population-based study.
Marko Kielinen, Heikki Rantala, Eija Timonen, Sirkka-Liisa Linna, Irma Moilanen. Autism 2004
115
11


Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
Maricela Alarcón, Rita M Cantor, Jianjun Liu, T Conrad Gilliam, Daniel H Geschwind. Am J Hum Genet 2002
203
10

A genomewide screen of 345 families for autism-susceptibility loci.
Amanda L Yonan, Maricela Alarcón, Rong Cheng, Patrik K E Magnusson, Sarah J Spence, Abraham A Palmer, Adina Grunn, Suh-Hang Hank Juo, Joseph D Terwilliger, Jianjun Liu,[...]. Am J Hum Genet 2003
207
10

Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders.
MarcosRobertoHigino Estécio, Agnes Cristina Fett-Conte, Marileila Varella-Garcia, Cíntia Fridman, Ana Elizabete Silva. J Autism Dev Disord 2002
22
45

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.
J A S Vorstman, W G Staal, E van Daalen, H van Engeland, P F R Hochstenbach, L Franke. Mol Psychiatry 2006
204
10

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
10


The epidemiology of autism: a review.
E Fombonne. Psychol Med 1999
500
9

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
E L Nurmi, Y Bradford, Y Chen, J Hall, B Arnone, M B Gardiner, H B Hutcheson, J R Gilbert, M A Pericak-Vance, S A Copeland-Yates,[...]. Genomics 2001
110
9

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions.
D H Geschwind, J Sowinski, C Lord, P Iversen, J Shestack, P Jones, L Ducat, S J Spence. Am J Hum Genet 2001
233
9

Prevalence of the fragile X anomaly amongst autistic twins and singletons.
A Bailey, P Bolton, L Butler, A Le Couteur, M Murphy, S Scott, T Webb, M Rutter. J Child Psychol Psychiatry 1993
80
11

Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletion.
Daynna J Wolff, Kimberly Clifton, Cynthia Karr, Jane Charles. Genet Med 2002
38
23

Identification of MeCP2 mutations in a series of females with autistic disorder.
Regina M Carney, Chantelle M Wolpert, Sarah A Ravan, Mona Shahbazian, Allison Ashley-Koch, Michael L Cuccaro, Jeffery M Vance, Margaret A Pericak-Vance. Pediatr Neurol 2003
157
9

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
Yujun Shao, M L Cuccaro, E R Hauser, K L Raiford, M M Menold, C M Wolpert, S A Ravan, L Elston, K Decena, S L Donnelly,[...]. Am J Hum Genet 2003
248
9


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.