A citation-based method for searching scientific literature

Christian Wentzel, Maria Fernström, Ylva Ohrner, Göran Annerén, Ann-Charlotte Thuresson. Eur J Med Genet 2008
Times Cited: 109







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



Times Cited
  Times     Co-cited
Similarity


Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
Regina E Ensenauer, Adewale Adeyinka, Heather C Flynn, Virginia V Michels, Noralane M Lindor, D Brian Dawson, Erik C Thorland, Cindy Pham Lorentz, Jennifer L Goldstein, Marie T McDonald,[...]. Am J Hum Genet 2003
253
43

Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
Zhishuo Ou, Jonathan S Berg, Hagith Yonath, Victoria B Enciso, David T Miller, Jonathan Picker, Tiffanee Lenzi, Catherine E Keegan, Vernon R Sutton, John Belmont,[...]. Genet Med 2008
134
40

Microduplication 22q11.2: a new chromosomal syndrome.
Marie-France Portnoï. Eur J Med Genet 2009
145
39

Microduplication and triplication of 22q11.2: a highly variable syndrome.
Twila M Yobb, Martin J Somerville, Lionel Willatt, Helen V Firth, Karen Harrison, Jennifer MacKenzie, Natasha Gallo, Bernice E Morrow, Lisa G Shaffer, Melanie Babcock,[...]. Am J Hum Genet 2005
172
33

A common molecular basis for rearrangement disorders on chromosome 22q11.
L Edelmann, R K Pandita, E Spiteri, B Funke, R Goldberg, N Palanisamy, R S Chaganti, E Magenis, R J Shprintzen, B E Morrow. Hum Mol Genet 1999
336
24

Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
Justine Coppinger, Donna McDonald-McGinn, Elaine Zackai, Kate Shane, Joan F Atkin, Alexander Asamoah, Robert Leland, David D Weaver, Susan Lansky-Shafer, Karen Schmidt,[...]. Hum Mol Genet 2009
55
34


22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.
Marie-France Portnoï, Fanny Lebas, Nicolas Gruchy, Azarnouche Ardalan, Valérie Biran-Mucignat, Valérie Malan, Lina Finkel, Gilles Roger, Sarah Ducrocq, Francis Gold,[...]. Am J Med Genet A 2005
78
23

The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies.
Céline de La Rochebrochard, Géraldine Joly-Hélas, Alice Goldenberg, Isabelle Durand, Annie Laquerrière, Valentine Ickowicz, Pascale Saugier-Veber, Danièle Eurin, Hélène Moirot, Alain Diguet,[...]. Am J Med Genet A 2006
55
29

Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication.
S Yu, K Cox, K Friend, S Smith, R Buchheim, S Bain, J Liebelt, E Thompson, D Bratkovic. Clin Genet 2008
34
47

1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.
A Alberti, C Romano, M Falco, F Calì, P Schinocca, O Galesi, A Spalletta, D Di Benedetto, M Fichera. Clin Genet 2007
44
34

A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome.
S J Hassed, D Hopcus-Niccum, L Zhang, S Li, J J Mulvihill. Clin Genet 2004
68
22

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf,[...]. Hum Mol Genet 2000
376
15

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
14

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening.
Tara L Wenger, Judith S Miller, Lauren M DePolo, Ashley B de Marchena, Caitlin C Clements, Beverly S Emanuel, Elaine H Zackai, Donna M McDonald-McGinn, Robert T Schultz. Mol Autism 2016
40
35

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
408
13

Distal 22q11.2 microduplication encompassing the BCR gene.
Maria Descartes, Judy Franklin, Teresita Diaz de Ståhl, Arkadiusz Piotrowski, Carl E G Bruder, Jan P Dumanski, Andrew J Carroll, Fady M Mikhail. Am J Med Genet A 2008
29
44


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
11

A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review.
Luis Fernández, Julián Nevado, Fernando Santos, Damià Heine-Suñer, Victor Martinez-Glez, Sixto García-Miñaur, Rebeca Palomo, Alicia Delicado, Isidora López Pajares, María Palomares,[...]. BMC Med Genet 2009
46
23

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
736
10

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
514
10

Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.
Tamim H Shaikh, Ronald J O'Connor, Mary Ella Pierpont, James McGrath, April M Hacker, Manjunath Nimmakayalu, Elizabeth Geiger, Beverly S Emanuel, Sulagna C Saitta. Genome Res 2007
90
11

Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.
S Van Campenhout, K Devriendt, J Breckpot, J-P Frijns, H Peeters, G Van Buggenhout, H Van Esch, B Maes, A Swillen. Genet Couns 2012
26
38

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
819
9

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
389
9

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
523
9

Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions.
Christiane Zweier, Heinrich Sticht, Inci Aydin-Yaylagül, Christine E Campbell, Anita Rauch. Am J Hum Genet 2007
141
9

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice.
Go Suzuki, Kathryn M Harper, Takeshi Hiramoto, Birgit Funke, MoonSook Lee, Gina Kang, Mahalah Buell, Mark A Geyer, Raju Kucherlapati, Bernice Morrow,[...]. Hum Mol Genet 2009
35
25

Genomic disorders on 22q11.
Heather E McDermid, Bernice E Morrow. Am J Hum Genet 2002
172
9

Evidence that duplications of 22q11.2 protect against schizophrenia.
E Rees, G Kirov, A Sanders, J T R Walters, K D Chambert, J Shi, J Szatkiewicz, C O'Dushlaine, A L Richards, E K Green,[...]. Mol Psychiatry 2014
82
10

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
199
8

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage.
Jun Liao, Lazaros Kochilas, Sonja Nowotschin, Jelena S Arnold, Vimla S Aggarwal, Jonathan A Epstein, M Christian Brown, Joe Adams, Bernice E Morrow. Hum Mol Genet 2004
164
8

Autistic disorder and 22q11.2 duplication.
Nahit Motavalli Mukaddes, Sabri Herguner. World J Biol Psychiatry 2007
47
17


An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairment.
Céline Pebrel-Richard, Stéphan Kemeny, Laetitia Gouas, Eléonore Eymard-Pierre, Nathalie Blanc, Christine Francannet, Andreï Tchirkov, Carole Goumy, Philippe Vago. Eur J Med Genet 2012
14
57

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.
J Wincent, D L Bruno, B W M van Bon, A Bremer, H Stewart, E M H F Bongers, C W Ockeloen, M H Willemsen, D D A Keays, G Baird,[...]. Mol Syndromol 2010
19
42

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
8

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
270
7

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
D M McDonald-McGinn, R Kirschner, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, C Solot, P Wang, I Jacobs,[...]. Genet Couns 1999
311
7

Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2.
A Rauch, S Zink, C Zweier, C T Thiel, A Koch, R Rauch, J Lascorz, U Hüffmeier, M Weyand, H Singer,[...]. J Med Genet 2005
107
7

Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
Anna Brunet, Elisabeth Gabau, Rosa Maria Perich, Laura Valdesoiro, Carme Brun, Maria Rosa Caballín, Miriam Guitart. Am J Med Genet A 2006
31
22

Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.
Gian Paolo Ramelli, Charlotte Silacci, Alessandra Ferrarini, Claudio Cattaneo, Paola Visconti, Graziano Pescia. Dev Med Child Neurol 2008
23
30

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
7

22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
Shay Ben-Shachar, Zhishuo Ou, Chad A Shaw, John W Belmont, Millan S Patel, Marybeth Hummel, Stephen Amato, Nicole Tartaglia, Jonathan Berg, V Reid Sutton,[...]. Am J Hum Genet 2008
134
7


Phenotypic variability of distal 22q11.2 copy number abnormalities.
Tiong Yang Tan, Amanda Collins, Paul A James, George McGillivray, Zornitza Stark, Christopher T Gordon, Richard J Leventer, Kate Pope, Robin Forbes, John A Crolla,[...]. Am J Med Genet A 2011
43
16

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
7

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
7

Ocular manifestations of 22q11.2 microduplication.
Jose A Cordovez, Jenina Capasso, Michelle D Lingao, Karthikeyan A Sadagopan, George L Spaeth, Barry N Wasserman, Alex V Levin. Ophthalmology 2014
12
58


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.