A citation-based method for searching scientific literature

Aline L Petrin, Sandra Daack-Hirsch, Jamie L'Heureux, Jeffrey C Murray. Cleft Palate Craniofac J 2011
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
23
71

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
71

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
71

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
57

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
161
57

The 3q29 microdeletion syndrome: report of three new unrelated patients and in silico "RNA binding" analysis of the 3q29 region.
Majed J Dasouki, Gerald H Lushington, Karine Hovanes, James Casey, Mereceds Gorre. Am J Med Genet A 2011
12
57

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
64
57

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
42

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
42

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
42

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
161
42

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
28

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
158
28

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
28


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
28

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
89
28

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
28

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
28



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
28

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
28

Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb.
Adewale Adeyinka, Kimberly J Stockero, Heather C Flynn, Cindy P Lorentz, Rhett P Ketterling, Syed M Jalal. Genet Med 2004
19
14


Familial deletion of chromosome 18 (p11.2).
G V Velagaleti, S Harris, N J Carpenter, J Coldwell, B Say. Ann Genet 1996
23
14

Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome.
Douglas R Stewart, Alina Huang, Francesca Faravelli, Britt-Marie Anderlid, Livija Medne, Karen Ciprero, Maninder Kaur, Elena Rossi, Romano Tenconi, Magnus Nordenskjöld,[...]. Am J Med Genet A 2004
45
14


Deletion of 22q11 in two brothers with different phenotype.
L Kasprzak, V M Der Kaloustian, A M Elliott, M Shevell, C Lejtenyi, P Eydoux. Am J Med Genet 1998
23
14

A family with a grand-maternally derived interstitial duplication of proximal 15q.
F Z Boyar, M M Whitney, A C Lossie, B A Gray, K L Keller, H J Stalker, R T Zori, G Geffken, J Mutch, P J Edge,[...]. Clin Genet 2001
40
14

Genome architecture catalyzes nonrecurrent chromosomal rearrangements.
Paweł Stankiewicz, Christine J Shaw, Jason D Dapper, Keiko Wakui, Lisa G Shaffer, Marjorie Withers, Leah Elizondo, Sung-Sup Park, James R Lupski. Am J Hum Genet 2003
145
14

Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination.
Katharina Steinmann, David N Cooper, Lan Kluwe, Nadia A Chuzhanova, Cornelia Senger, Eduard Serra, Conxi Lazaro, Montserrat Gilaberte, Katharina Wimmer, Viktor-Felix Mautner,[...]. Am J Hum Genet 2007
46
14

Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion.
J-S Fang, K-F Lee, C-T Huang, C-L Syu, K-J Yang, L-H Wang, D-L Liao, C-H Chen. Clin Genet 2008
10
14

Recurrent DNA inversion rearrangements in the human genome.
Margarita Flores, Lucía Morales, Claudia Gonzaga-Jauregui, Rocío Domínguez-Vidaña, Cinthya Zepeda, Omar Yañez, María Gutiérrez, Tzitziki Lemus, David Valle, Ma Carmen Avila,[...]. Proc Natl Acad Sci U S A 2007
63
14

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.
Blake C Ballif, Emily A Rorem, Kyle Sundin, Matt Lincicum, Shannon Gaskin, Justine Coppinger, Catherine D Kashork, Lisa G Shaffer, Bassem A Bejjani. Am J Med Genet A 2006
208
14

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
471
14


Clinical and molecular characterization of a patient with Langer-Giedion syndrome and mosaic del(8)(q22.3q24.13).
Alan L Shanske, Ankita Patel, Sou Saukam, Brynn Levy, Hermann-Josef Lüdecke. Am J Med Genet A 2008
13
14

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion.
R T Zori, J R Lupski, Z Heju, F Greenberg, J M Killian, B A Gray, D J Driscoll, P I Patel, J L Zackowski. Am J Med Genet 1993
67
14

Familial 5p- syndrome.
T Kushnick, K W Rao, A N Lamb. Clin Genet 1984
20
14

Familial interstitial deletion of chromosome 4 (p15.2p16.1).
Vijay S Tonk, Syed M Jalal, Jose Gonzalez, Amantia Kennedy, Gopalrao V N Velagaleti. Ann Genet 2003
12
14

Interstitial 2.2 Mb deletion at 9q34 in a patient with mental retardation but without classical features of the 9q subtelomeric deletion syndrome.
Tjitske Kleefstra, David A Koolen, Willy M Nillesen, Nicole de Leeuw, Ben C J Hamel, Joris A Veltman, Erik A Sistermans, Hans van Bokhoven, Conny van Ravenswaay, Bert B A de Vries. Am J Med Genet A 2006
19
14

Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.
T Kleefstra, M Smidt, M J G Banning, A R Oudakker, H Van Esch, A P M de Brouwer, W Nillesen, E A Sistermans, B C J Hamel, D de Bruijn,[...]. J Med Genet 2005
121
14

The chromosome 9q subtelomere deletion syndrome.
Douglas R Stewart, Tjitske Kleefstra. Am J Med Genet C Semin Med Genet 2007
69
14

Direct transmission of the 18q- syndrome from mother to daughter.
C P Chen, S P Lin, S R Chern, C C Lee, J K Huang, W Wang. Genet Couns 2006
8
14

Somatic mosaicism for copy number variation in differentiated human tissues.
Arkadiusz Piotrowski, Carl E G Bruder, Robin Andersson, Teresita Diaz de Ståhl, Uwe Menzel, Johanna Sandgren, Andrzej Poplawski, Desiree von Tell, Chiquito Crasto, Adam Bogdan,[...]. Hum Mutat 2008
152
14

Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome.
Tjitske Kleefstra, Han G Brunner, Jeanne Amiel, Astrid R Oudakker, Willy M Nillesen, Alex Magee, David Geneviève, Valérie Cormier-Daire, Hilde van Esch, Jean-Pierre Fryns,[...]. Am J Hum Genet 2006
242
14

Behavioral phenotype in the 9q subtelomeric deletion syndrome: a report about two adult patients.
Willem M A Verhoeven, Tjitske Kleefstra, Jos I M Egger. Am J Med Genet B Neuropsychiatr Genet 2010
19
14

Familial deletion 18p syndrome: case report.
Bruno Maranda, Nicole Lemieux, Emmanuelle Lemyre. BMC Med Genet 2006
29
14

Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
T Kleefstra, W A van Zelst-Stams, W M Nillesen, V Cormier-Daire, G Houge, N Foulds, M van Dooren, M H Willemsen, R Pfundt, A Turner,[...]. J Med Genet 2009
126
14


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.