A citation-based method for searching scientific literature

Majed J Dasouki, Gerald H Lushington, Karine Hovanes, James Casey, Mereceds Gorre. Am J Med Genet A 2011
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.
Lionel Willatt, James Cox, John Barber, Elisabet Dachs Cabanas, Amanda Collins, Dian Donnai, David R FitzPatrick, Eddy Maher, Howard Martin, Josep Parnau,[...]. Am J Hum Genet 2005
159
69

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review.
Fabiola Quintero-Rivera, Pantea Sharifi-Hannauer, Julian A Martinez-Agosto. Am J Med Genet A 2010
63
69

1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.
William Cobb, Arne Anderson, Clesson Turner, Ruth D Hoffman, Steven Schonberg, Sondra W Levin. Eur J Med Genet 2010
17
61

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich,[...]. Mol Cytogenet 2008
162
61

3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.
Feng Li, Emily C Lisi, Elizabeth S Wohler, Ada Hamosh, Denise A S Batista. Eur J Med Genet 2009
24
61

3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs.
Maria Cristina Digilio, Laura Bernardini, Rita Mingarelli, Rossella Capolino, Anna Capalbo, Maria Grazia Giuffrida, Paolo Versacci, Antonio Novelli, Bruno Dallapiccola. Am J Med Genet A 2009
28
61

Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.
Jill Clayton-Smith, Carol Giblin, Rupert A Smith, Carolyn Dunn, Lionel Willatt. Clin Dysmorphol 2010
28
53

Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.
Angela Sagar, Jeffrey R Bishop, D Clare Tessman, Steve Guter, Christa L Martin, Edwin H Cook. Am J Med Genet A 2013
31
53

Microdeletions of 3q29 confer high risk for schizophrenia.
Jennifer Gladys Mulle, Anne F Dodd, John A McGrath, Paula S Wolyniec, Adele A Mitchell, Amol C Shetty, Nara L Sobreira, David Valle, M Katharine Rudd, Glen Satten,[...]. Am J Hum Genet 2010
159
46

Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations.
E Rossi, F Piccini, M Zollino, G Neri, D Caselli, R Tenconi, C Castellan, R Carrozzo, C Danesino, O Zuffardi,[...]. J Med Genet 2001
106
46

Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
Megan R Glassford, Jill A Rosenfeld, Alexa A Freedman, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2016
39
46


Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
Douglas F Levinson, Jubao Duan, Sang Oh, Kai Wang, Alan R Sanders, Jianxin Shi, Nancy Zhang, Bryan J Mowry, Ann Olincy, Farooq Amin,[...]. Am J Psychiatry 2011
316
30

A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications.
Aline L Petrin, Sandra Daack-Hirsch, Jamie L'Heureux, Jeffrey C Murray. Cleft Palate Craniofac J 2011
7
57

1.6Mb deletion in chromosome band 3q29 associated with eye abnormalities.
Nataliya Tyshchenko, Karl Hackmann, Eva-Maria Gerlach, Teresa Neuhann, Evelin Schrock, Sigrid Tinschert. Eur J Med Genet 2009
17
30

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.
A C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, M R Passos-Bueno, J Knijnenburg, K Szuhai, W Sloos, J F Mazzeu, F Kok, C Cheroki,[...]. Cytogenet Genome Res 2006
86
30

3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.
Santina Città, Serafino Buono, Donatella Greco, Concetta Barone, Enrico Alfei, Sara Bulgheroni, Arianna Usilla, Chiara Pantaleoni, Corrado Romano. Am J Med Genet A 2013
12
33


Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia.
L S Carroll, H J Williams, J Walters, G Kirov, M C O'Donovan, M J Owen. Am J Med Genet B Neuropsychiatr Genet 2011
20
23

3q29 interstitial microduplication: a new syndrome in a three-generation family.
Emily C Lisi, Ada Hamosh, Kimberly F Doheny, Elizabeth Squibb, Barbara Jackson, Rebecca Galczynski, George H Thomas, Denise A S Batista. Am J Med Genet A 2008
54
23

Copy number variation in schizophrenia in Sweden.
J P Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, J L Moran, B M Neale, M Fromer, D Ruderfer, S Akterin, S E Bergen,[...]. Mol Psychiatry 2014
161
23

Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genes.
S Monfort, M Roselló, C Orellana, S Oltra, D Blesa, K Kok, I Ferrer, J C Cigudosa, F Martínez. J Med Genet 2008
41
23

Fbxo45, a novel ubiquitin ligase, regulates synaptic activity.
Hirobumi Tada, Hirotaka James Okano, Hiroshi Takagi, Shinsuke Shibata, Ikuko Yao, Masaki Matsumoto, Toru Saiga, Keiichi I Nakayama, Haruo Kashima, Takuya Takahashi,[...]. J Biol Chem 2010
57
15


An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
287
15

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
Daniel Moreno-De-Luca, Jennifer G Mulle, Erin B Kaminsky, Stephan J Sanders, Scott M Myers, Margaret P Adam, Amy T Pakula, Nancy J Eisenhauer, Kim Uhas, LuAnn Weik,[...]. Am J Hum Genet 2010
198
15

Fbxo45 forms a novel ubiquitin ligase complex and is required for neuronal development.
Toru Saiga, Takaichi Fukuda, Masaki Matsumoto, Hirobumi Tada, Hirotaka James Okano, Hideyuki Okano, Keiichi I Nakayama. Mol Cell Biol 2009
78
15



16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders.
Arivudainambi Ramalingam, Xin-Gang Zhou, Stephanie D Fiedler, Sarah J Brawner, Julie M Joyce, Hong-Yu Liu, Shihui Yu. J Hum Genet 2011
71
15

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
15

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
15

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
518
15

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.
Detelina Grozeva, Donald F Conrad, Chris P Barnes, Matthew Hurles, Michael J Owen, Michael C O'Donovan, Nick Craddock, George Kirov. Schizophr Res 2012
61
15

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.
Larissa R Stewart, April L Hall, Sung-Hae L Kang, Chad A Shaw, Arthur L Beaudet. BMC Med Genet 2011
48
15


Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.
S Goobie, J Knijnenburg, D Fitzpatrick, F H Sharkey, A C Lionel, C R Marshall, T Azam, M Shago, K Chong, R Mendoza-Londono,[...]. Cytogenet Genome Res 2008
28
15


Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
Lina Shao, Chad A Shaw, Xin-Yan Lu, Trilochan Sahoo, Carlos A Bacino, Seema R Lalani, Pawel Stankiewicz, Svetlana A Yatsenko, Yinfeng Li, Sarah Neill,[...]. Am J Med Genet A 2008
88
15

Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
D A Koolen, W M Nillesen, M H A Versteeg, G F M Merkx, N V A M Knoers, M Kets, S Vermeer, C M A van Ravenswaaij, C G de Kovel, H G Brunner,[...]. J Med Genet 2004
119
15

The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage.
Grant S Stewart, Stephanie Panier, Kelly Townsend, Abdallah K Al-Hakim, Nadine K Kolas, Edward S Miller, Shinichiro Nakada, Jarkko Ylanko, Signe Olivarius, Megan Mendez,[...]. Cell 2009
530
15

Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.
Chenyao Wang, Takayoshi Koide, Hiroki Kimura, Shohko Kunimoto, Akira Yoshimi, Yukako Nakamura, Itaru Kushima, Masahiro Banno, Naoko Kawano, Yuto Takasaki,[...]. Schizophr Res 2014
10
20

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders.
Daniel J Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P Carter, Martyn L Blayney, Stephan Beck, Matthew E Hurles. Nat Genet 2008
214
15

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
614
15

Copy number variation in bipolar disorder.
E K Green, E Rees, J T R Walters, K-G Smith, L Forty, D Grozeva, J L Moran, P Sklar, S Ripke, K D Chambert,[...]. Mol Psychiatry 2016
92
15


Genome destabilization by homologous recombination in the germ line.
Mariko Sasaki, Julian Lange, Scott Keeney. Nat Rev Mol Cell Biol 2010
140
15

In vivo engineering of oncogenic chromosomal rearrangements with the CRISPR/Cas9 system.
Danilo Maddalo, Eusebio Manchado, Carla P Concepcion, Ciro Bonetti, Joana A Vidigal, Yoon-Chi Han, Paul Ogrodowski, Alessandra Crippa, Natasha Rekhtman, Elisa de Stanchina,[...]. Nature 2014
339
15

Population analysis of large copy number variants and hotspots of human genetic disease.
Andy Itsara, Gregory M Cooper, Carl Baker, Santhosh Girirajan, Jun Li, Devin Absher, Ronald M Krauss, Richard M Myers, Paul M Ridker, Daniel I Chasman,[...]. Am J Hum Genet 2009
419
15

Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.
Derek J C Tai, Ashok Ragavendran, Poornima Manavalan, Alexei Stortchevoi, Catarina M Seabra, Serkan Erdin, Ryan L Collins, Ian Blumenthal, Xiaoli Chen, Yiping Shen,[...]. Nat Neurosci 2016
30
15


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.