A citation-based method for searching scientific literature

Jannine D Cody, Courtney Sebold, Amtul Malik, Patricia Heard, Erika Carter, Analisa Crandall, Bridgette Soileau, Margaret Semrud-Clikeman, Catherine M Cody, L Jean Hardies, Jinqi Li, Jack Lancaster, Peter T Fox, Robert F Stratton, Brian Perry, Daniel E Hale. Am J Med Genet A 2007
Times Cited: 26







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



Times Cited
  Times     Co-cited
Similarity


Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.
Ilse Feenstra, Lisenka E L M Vissers, Mirjam Orsel, Ad Geurts van Kessel, Han G Brunner, Joris A Veltman, Conny M A van Ravenswaaij-Arts. Am J Med Genet A 2007
91
57

Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome.
Karen Buysse, Björn Menten, Ann Oostra, Sylvie Tavernier, Geert R Mortier, Frank Speleman. Am J Med Genet A 2008
25
52

Long-term survival in a patient with del(18)(q12.2q21.1).
Brad T Tinkle, Carol A Christianson, Elizabeth K Schorry, Thomas Webb, Robert J Hopkin. Am J Med Genet A 2003
20
40

Del(18)(q12.2q21.1) caused by a paternal sister chromatid rearrangement in a developmentally delayed girl.
Dieter Kotzot, Edda Haberlandt, Christine Fauth, Sara Baumgartner, Sabine Scholl-Bürgi, Gerd Utermann. Am J Med Genet A 2005
11
63

Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype.
A Schinzel, F Binkert, D M Lillington, M Sands, R J Stocks, R H Lindenbaum, H Matthews, H Sheridan. J Med Genet 1991
32
26

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome.
Alexander Hoischen, Bregje W M van Bon, Christian Gilissen, Peer Arts, Bart van Lier, Marloes Steehouwer, Petra de Vries, Rick de Reuver, Nienke Wieskamp, Geert Mortier,[...]. Nat Genet 2010
320
26

A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay.
Sonia Bouquillon, Joris Andrieux, Emilie Landais, Bénédicte Duban-Bedu, Françoise Boidein, Bruno Lenne, Louis Vallée, Teresinha Leal, Martine Doco-Fenzy, Bruno Delobel. Eur J Med Genet 2011
17
41

Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q.
J D Cody, P D Ghidoni, B R DuPont, D E Hale, S G Hilsenbeck, R F Stratton, D S Hoffman, S Muller, R L Schaub, R J Leach,[...]. Am J Med Genet 1999
93
23

Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome.
Isabel Filges, Keiko Shimojima, Nobuhiko Okamoto, Benno Röthlisberger, Peter Weber, Andreas R Huber, Tsutomu Nishizawa, Alexandre N Datta, Peter Miny, Toshiyuki Yamamoto. J Med Genet 2011
46
23

Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.
M Poissonnier, C Turleau, M Olivier-Martin, M J Milleret-Proyart, M Prieur, M Dubos, M O Cabanis, F Mugneret, P Blanc, L Noel. Ann Genet 1992
18
27

High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH).
Patricia L Heard, Erika M Carter, Analisa C Crandall, Courtney Sebold, Daniel E Hale, Jannine D Cody. Am J Med Genet A 2009
38
19

Familial mental retardation in a family with an inherited chromosome rearrangement.
A E Chudley, F Bauder, M Ray, P J McAlpine, S D Pena, J L Hamerton. J Med Genet 1974
72
15

Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.
J J Engelen, W J Loots, J C Albrechts, A S Plomp, S B van der Meer, J S Vles, G J Hamers, J P Geraedts. Am J Med Genet 1998
12
33


Molecular characterisation of a proximal chromosome 18q deletion.
M McEntagart, A Carey, C Breen, S McQuaid, R L Stallings, A J Green, M D King. J Med Genet 2001
12
33

Narrowing critical regions and determining penetrance for selected 18q- phenotypes.
Jannine D Cody, Patricia L Heard, Analisa C Crandall, Erika M Carter, John Li, L Jean Hardies, Jack Lancaster, Brian Perry, Robert F Stratton, Courtney Sebold,[...]. Am J Med Genet A 2009
35
15

372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.
Giuseppina Marseglia, Maria Rosaria Scordo, Chiara Pescucci, Genni Nannetti, Elisabetta Biagini, Valeria Scandurra, Francesca Gerundino, Alberto Magi, Matteo Benelli, Francesca Torricelli. Eur J Med Genet 2012
32
15

18q deletions: clinical, molecular, and brain MRI findings of 14 individuals.
Tarja Linnankivi, Pentti Tienari, Mirja Somer, Marketta Kähkönen, Tuula Lönnqvist, Leena Valanne, Helena Pihko. Am J Med Genet A 2006
48
11

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
11

Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET.
M Minakuchi, N Kakazu, M J Gorrin-Rivas, T Abe, T D Copeland, K Ueda, Y Adachi. Eur J Biochem 2001
58
11

Strong synaptic transmission impact by copy number variations in schizophrenia.
Joseph T Glessner, Muredach P Reilly, Cecilia E Kim, Nagahide Takahashi, Anthony Albano, Cuiping Hou, Jonathan P Bradfield, Haitao Zhang, Patrick M A Sleiman, James H Flory,[...]. Proc Natl Acad Sci U S A 2010
142
11

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
S M Gribble, E Prigmore, D C Burford, K M Porter, Bee Ling Ng, E J Douglas, H Fiegler, P Carr, D Kalaitzopoulos, S Clegg,[...]. J Med Genet 2005
161
11


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

SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome.
K Suphapeetiporn, C Srichomthong, V Shotelersuk. Clin Genet 2011
20
15


Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.
Lisenka E L M Vissers, Bert B A de Vries, Kazutoyo Osoegawa, Irene M Janssen, Ton Feuth, Chik On Choy, Huub Straatman, Walter van der Vliet, Erik H L P G Huys, Anke van Rijk,[...]. Am J Hum Genet 2003
342
7

Small GTPase proteins Rin and Rit Bind to PAR6 GTP-dependently and regulate cell transformation.
Mitsunobu Hoshino, Tamotsu Yoshimori, Shun Nakamura. J Biol Chem 2005
22
9


Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].
L C Surh, D H Ledbetter, F Greenberg. Am J Med Genet 1991
14
14


Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
J Schoumans, C Ruivenkamp, E Holmberg, M Kyllerman, B-M Anderlid, M Nordenskjöld. J Med Genet 2005
144
7

Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
M G Wilson, J W Towner, I Forsman, E Siris. Am J Med Genet 1979
98
7


The spectrum of growth abnormalities in children with 18q deletions.
D E Hale, J D Cody, J Baillargeon, R Schaub, M M Danney, R J Leach. J Clin Endocrinol Metab 2000
36
7

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
7

Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation.
Ulrika Wester, Marie-Louise Bondeson, Christina Edeby, Göran Annerén. Am J Med Genet A 2006
61
7

Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
461
7

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
7

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
7

Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning.
David Ng, Graham M Pitcher, Rachel K Szilard, Andréa Sertié, Marijana Kanisek, Steven J Clapcote, Tatiana Lipina, Lorraine V Kalia, Daisy Joo, Colin McKerlie,[...]. PLoS Biol 2009
123
7

Mapping and sequencing of structural variation from eight human genomes.
Jeffrey M Kidd, Gregory M Cooper, William F Donahue, Hillary S Hayden, Nick Sampas, Tina Graves, Nancy Hansen, Brian Teague, Can Alkan, Francesca Antonacci,[...]. Nature 2008
765
7

Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).
Ioannis Panagopoulos, Gitte Kerndrup, Niels Carlsen, Bodil Strömbeck, Margareth Isaksson, Bertil Johansson. Br J Haematol 2007
34
7

Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays.
Damien L Bruno, Zornitza Stark, David J Amor, Trent Burgess, Kathy Butler, Sylvea Corrie, David Francis, Devika Ganesamoorthy, Louise Hills, Paul A James,[...]. Hum Mutat 2011
34
7

Accurate distinction of pathogenic from benign CNVs in mental retardation.
Jayne Y Hehir-Kwa, Nienke Wieskamp, Caleb Webber, Rolph Pfundt, Han G Brunner, Christian Gilissen, Bert B A de Vries, Chris P Ponting, Joris A Veltman. PLoS Comput Biol 2010
42
7


Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity.
Christina Halgren, Iben Bache, Mads Bak, Mikkel Wanting Myatt, Claire Marie Anderson, Karen Brøndum-Nielsen, Niels Tommerup. Eur J Hum Genet 2012
19
10

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
7

The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions.
Minire Hasi, Bridgette Soileau, Courtney Sebold, Annice Hill, Daniel E Hale, Louise O'Donnell, Jannine D Cody. Hum Genet 2011
27
7

Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humans.
Ilse Feenstra, Lisenka E L M Vissers, Ronald J E Pennings, Willy Nillessen, Rolph Pfundt, Henricus P Kunst, Ronald J Admiraal, Joris A Veltman, Conny M A van Ravenswaaij-Arts, Han G Brunner,[...]. Am J Hum Genet 2011
26
7


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.