A citation-based method for searching scientific literature

Herbert M Lachman, Erika Pedrosa, Oriana A Petruolo, Melissa Cockerham, Alexander Papolos, Tomas Novak, Demitri F Papolos, Pavla Stopkova. Am J Med Genet B Neuropsychiatr Genet 2007
Times Cited: 97







List of co-cited articles
1353 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
35

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Tom Walsh, Jon M McClellan, Shane E McCarthy, Anjené M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari,[...]. Science 2008
29

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
27

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
27


Large-scale copy number polymorphism in the human genome.
Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Pär Lundin, Susanne Månér, Hillary Massa, Megan Walker, Maoyen Chi,[...]. Science 2004
24

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
24

Whole-genome association study of bipolar disorder.
P Sklar, J W Smoller, J Fan, M A R Ferreira, R H Perlis, K Chambert, V L Nimgaonkar, M B McQueen, S V Faraone, A Kirby,[...]. Mol Psychiatry 2008
496
22


A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
A E Baum, N Akula, M Cabanero, I Cardona, W Corona, B Klemens, T G Schulze, S Cichon, M Rietschel, M M Nöthen,[...]. Mol Psychiatry 2008
482
21

DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.
Gary M Wilson, Stephane Flibotte, Vikramjit Chopra, Brianna L Melnyk, William G Honer, Robert A Holt. Hum Mol Genet 2006
132
19

Structural variation in the human genome.
Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
19

Relative impact of nucleotide and copy number variation on gene expression phenotypes.
Barbara E Stranger, Matthew S Forrest, Mark Dunning, Catherine E Ingle, Claude Beazley, Natalie Thorne, Richard Redon, Christine P Bird, Anna de Grassi, Charles Lee,[...]. Science 2007
18

Strong association of de novo copy number mutations with sporadic schizophrenia.
Bin Xu, J Louw Roos, Shawn Levy, E J van Rensburg, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2008
584
18

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility.
Enrique Gonzalez, Hemant Kulkarni, Hector Bolivar, Andrea Mangano, Racquel Sanchez, Gabriel Catano, Robert J Nibbs, Barry I Freedman, Marlon P Quinones, Michael J Bamshad,[...]. Science 2005
836
17

A molecular mechanism for the effect of lithium on development.
P S Klein, D A Melton. Proc Natl Acad Sci U S A 1996
17

Long-term response to lithium salts in bipolar illness is influenced by the glycogen synthase kinase 3-beta -50 T/C SNP.
Francesco Benedetti, Alessandro Serretti, Adriana Pontiggia, Alessandro Bernasconi, Cristina Lorenzi, Cristina Colombo, Enrico Smeraldi. Neurosci Lett 2005
134
17

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans.
Timothy J Aitman, Rong Dong, Timothy J Vyse, Penny J Norsworthy, Michelle D Johnson, Jennifer Smith, Jonathan Mangion, Cheri Roberton-Lowe, Amy J Marshall, Enrico Petretto,[...]. Nature 2006
518
16

Transgenic mice overexpressing glycogen synthase kinase 3beta: a putative model of hyperactivity and mania.
Jos Prickaerts, Dieder Moechars, Kim Cryns, Ilse Lenaerts, Hansfried van Craenendonck, Ilse Goris, Guy Daneels, J Adriaan Bouwknecht, Thomas Steckler. J Neurosci 2006
250
16

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans.
Yan Yang, Erwin K Chung, Yee Ling Wu, Stephanie L Savelli, Haikady N Nagaraja, Bi Zhou, Maddie Hebert, Karla N Jones, Yaoling Shu, Kathryn Kitzmiller,[...]. Am J Hum Genet 2007
321
15

A single nucleotide polymorphism in glycogen synthase kinase 3-beta promoter gene influences onset of illness in patients affected by bipolar disorder.
Francesco Benedetti, Alessandro Bernasconi, Cristina Lorenzi, Adriana Pontiggia, Alessandro Serretti, Cristina Colombo, Enrico Smeraldi. Neurosci Lett 2004
133
15

Singleton deletions throughout the genome increase risk of bipolar disorder.
D Zhang, L Cheng, Y Qian, N Alliey-Rodriguez, J R Kelsoe, T Greenwood, C Nievergelt, T B Barrett, R McKinney, N Schork,[...]. Mol Psychiatry 2009
104
15

A glycogen synthase kinase 3-beta promoter gene single nucleotide polymorphism is associated with age at onset and response to total sleep deprivation in bipolar depression.
Francesco Benedetti, Alessandro Serretti, Cristina Colombo, Cristina Lorenzi, Viviana Tubazio, Enrico Smeraldi. Neurosci Lett 2004
133
14

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
Manuel A R Ferreira, Michael C O'Donovan, Yan A Meng, Ian R Jones, Douglas M Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H Perlis, Elaine K Green,[...]. Nat Genet 2008
845
14

Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder.
Caroline M Nievergelt, Daniel F Kripke, Thomas B Barrett, Elyssa Burg, Ronald A Remick, A Dessa Sadovnick, Susan L McElroy, Paul E Keck, Nicholas J Schork, John R Kelsoe. Am J Med Genet B Neuropsychiatr Genet 2006
208
13

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
13

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
13

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
13

Mania-like behavior induced by disruption of CLOCK.
Kole Roybal, David Theobold, Ami Graham, Jennifer A DiNieri, Scott J Russo, Vaishnav Krishnan, Sumana Chakravarty, Joseph Peevey, Nathan Oehrlein, Shari Birnbaum,[...]. Proc Natl Acad Sci U S A 2007
520
12

Association analysis of the GSK-3beta T-50C gene polymorphism with schizophrenia and bipolar disorder.
Aleksandra Szczepankiewicz, Maria Skibinska, Joanna Hauser, Agnieszka Slopien, Anna Leszczynska-Rodziewicz, Paweł Kapelski, Monika Dmitrzak-Weglarz, Piotr M Czerski, Janusz K Rybakowski. Neuropsychobiology 2006
57
21

Copy-number variation and association studies of human disease.
Steven A McCarroll, David M Altshuler. Nat Genet 2007
405
12

Common deletion polymorphisms in the human genome.
Steven A McCarroll, Tracy N Hadnott, George H Perry, Pardis C Sabeti, Michael C Zody, Jeffrey C Barrett, Stephanie Dallaire, Stacey B Gabriel, Charles Lee, Mark J Daly,[...]. Nat Genet 2006
525
11

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
11

A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon.
Klaus Fellermann, Daniel E Stange, Elke Schaeffeler, Hartmut Schmalzl, Jan Wehkamp, Charles L Bevins, Walter Reinisch, Alexander Teml, Matthias Schwab, Peter Lichter,[...]. Am J Hum Genet 2006
384
11

Copy number variation: new insights in genome diversity.
Jennifer L Freeman, George H Perry, Lars Feuk, Richard Redon, Steven A McCarroll, David M Altshuler, Hiroyuki Aburatani, Keith W Jones, Chris Tyler-Smith, Matthew E Hurles,[...]. Genome Res 2006
488
11

Association study of the glycogen synthase kinase-3beta gene polymorphism with prophylactic lithium response in bipolar patients.
Aleksandra Szczepankiewicz, Janusz K Rybakowski, Aleksandra Suwalska, Maria Skibinska, Anna Leszczynska-Rodziewicz, Monika Dmitrzak-Weglarz, Piotr M Czerski, Joanna Hauser. World J Biol Psychiatry 2006
49
22

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
948
10

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.
Anne Rovelet-Lecrux, Didier Hannequin, Gregory Raux, Nathalie Le Meur, Annie Laquerrière, Anne Vital, Cécile Dumanchin, Sébastien Feuillette, Alexis Brice, Martine Vercelletto,[...]. Nat Genet 2006
810
10

Fine-scale structural variation of the human genome.
Eray Tuzun, Andrew J Sharp, Jeffrey A Bailey, Rajinder Kaul, V Anne Morrison, Lisa M Pertz, Eric Haugen, Hillary Hayden, Donna Albertson, Daniel Pinkel,[...]. Nat Genet 2005
713
10

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
10

Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia.
H A Mansour, J Wood, T Logue, K V Chowdari, M Dayal, D J Kupfer, T H Monk, B Devlin, V L Nimgaonkar. Genes Brain Behav 2006
184
10

No association of two common SNPs at position -1727 A/T, -50 C/T of GSK-3 beta polymorphisms with schizophrenia and bipolar disorder of Korean population.
Kyu Young Lee, Yong Min Ahn, Eun-Jeong Joo, Seong-Hoon Jeong, Jae Seung Chang, Seong-Chan Kim, Yong Sik Kim. Neurosci Lett 2006
48
20

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
George Kirov, Dilihan Gumus, Wei Chen, Nadine Norton, Lyudmila Georgieva, Murat Sari, Michael C O'Donovan, Fikret Erdogan, Michael J Owen, Hans-Hilger Ropers,[...]. Hum Mol Genet 2008
288
10



Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm.
Jiajun Shi, Jacqueline K Wittke-Thompson, Judith A Badner, Eiji Hattori, James B Potash, Virginia L Willour, Francis J McMahon, Elliot S Gershon, Chunyu Liu. Am J Med Genet B Neuropsychiatr Genet 2008
145
10

Convergent functional genomics of genome-wide association data for bipolar disorder: comprehensive identification of candidate genes, pathways and mechanisms.
H Le-Niculescu, S D Patel, M Bhat, R Kuczenski, S V Faraone, M T Tsuang, F J McMahon, N J Schork, J I Nurnberger, A B Niculescu. Am J Med Genet B Neuropsychiatr Genet 2009
146
10

Genome-wide association study of bipolar disorder in European American and African American individuals.
E N Smith, C S Bloss, J A Badner, T Barrett, P L Belmonte, W Berrettini, W Byerley, W Coryell, D Craig, H J Edenberg,[...]. Mol Psychiatry 2009
258
10

Evidence for genetic association of RORB with bipolar disorder.
Casey L McGrath, Stephen J Glatt, Pamela Sklar, Helen Le-Niculescu, Ronald Kuczenski, Alysa E Doyle, Joseph Biederman, Eric Mick, Stephen V Faraone, Alexander B Niculescu,[...]. BMC Psychiatry 2009
73
13

Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling.
Yingwei Mao, Xuecai Ge, Christopher L Frank, Jon M Madison, Angela N Koehler, Mary Kathryn Doud, Carlos Tassa, Erin M Berry, Takahiro Soda, Karun K Singh,[...]. Cell 2009
573
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.