A citation-based method for searching scientific literature

Andrey Shuvarikov, Ian M Campbell, Piotr Dittwald, Nicholas J Neill, Martin G Bialer, Christine Moore, Patricia G Wheeler, Stephanie E Wallace, Mark C Hannibal, Michael F Murray, Monica A Giovanni, Deborah Terespolsky, Sandi Sodhi, Matteo Cassina, David Viskochil, Billur Moghaddam, Kristin Herman, Chester W Brown, Christine R Beck, Anna Gambin, Sau Wai Cheung, Ankita Patel, Allen N Lamb, Lisa G Shaffer, Jay W Ellison, J Britt Ravnan, Paweł Stankiewicz, Jill A Rosenfeld. Hum Mutat 2013
Times Cited: 29







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



Times Cited
  Times     Co-cited
Similarity


A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features.
Anna-Maja Molin, J Andrieux, D A Koolen, V Malan, M Carella, L Colleaux, V Cormier-Daire, A David, N de Leeuw, B Delobel,[...]. J Med Genet 2012
41
31

Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination.
Ian M Campbell, Tomasz Gambin, Piotr Dittwald, Christine R Beck, Andrey Shuvarikov, Patricia Hixson, Ankita Patel, Anna Gambin, Chad A Shaw, Jill A Rosenfeld,[...]. BMC Biol 2014
41
24

Segmental duplications and copy-number variation in the human genome.
Andrew J Sharp, Devin P Locke, Sean D McGrath, Ze Cheng, Jeffrey A Bailey, Rhea U Vallente, Lisa M Pertz, Royden A Clark, Stuart Schwartz, Rick Segraves,[...]. Am J Hum Genet 2005
664
20

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
20


Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.
Barbara Wiśniowiecka-Kowalnik, Monika Kastory-Bronowska, Magdalena Bartnik, Katarzyna Derwińska, Wanda Dymczak-Domini, Dorota Szumbarska, Ewa Ziemka, Krzysztof Szczałuba, Maciej Sykulski, Tomasz Gambin,[...]. Eur J Hum Genet 2013
30
17

Zbtb20 is essential for the specification of CA1 field identity in the developing hippocampus.
Zhifang Xie, Xianhua Ma, Wenli Ji, Guangdi Zhou, Yinzhong Lu, Zhenghua Xiang, Yan X Wang, Lei Zhang, Yiping Hu, Yu-Qiang Ding,[...]. Proc Natl Acad Sci U S A 2010
62
17

A rare 3q13.31 microdeletion including GAP43 and LSAMP genes.
Stefania Gimelli, Massimiliano Leoni, Maja Di Rocco, Gianluca Caridi, Simona Porta, Cristina Cuoco, Giorgio Gimelli, Elisa Tassano. Mol Cytogenet 2013
7
71

Expanding the clinical phenotype at the 3q13.31 locus with a new case of microdeletion and first characterization of the reciprocal duplication.
Marie-Laure Vuillaume, Marie-Ange Delrue, Sophie Naudion, Jérôme Toutain, Patricia Fergelot, Benoit Arveiler, Didier Lacombe, Caroline Rooryck. Mol Genet Metab 2013
11
45

A recurrent translocation is mediated by homologous recombination between HERV-H elements.
Karen E Hermetz, Urvashi Surti, Jannine D Cody, M Katharine Rudd. Mol Cytogenet 2012
14
35

Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses.
C Sun, H Skaletsky, S Rozen, J Gromoll, E Nieschlag, R Oates, D C Page. Hum Mol Genet 2000
174
17

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Santhosh Girirajan, Megan Y Dennis, Carl Baker, Maika Malig, Bradley P Coe, Catarina D Campbell, Kenneth Mark, Tiffany H Vu, Can Alkan, Ze Cheng,[...]. Am J Hum Genet 2013
187
17


NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
Piotr Dittwald, Tomasz Gambin, Przemyslaw Szafranski, Jian Li, Stephen Amato, Michael Y Divon, Lisa Ximena Rodríguez Rojas, Lindsay E Elton, Daryl A Scott, Christian P Schaaf,[...]. Genome Res 2013
78
17

Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-over.
Pengfei Liu, Melanie Lacaria, Feng Zhang, Marjorie Withers, P J Hastings, James R Lupski. Am J Hum Genet 2011
74
17

Replicative mechanisms for CNV formation are error prone.
Claudia M B Carvalho, Davut Pehlivan, Melissa B Ramocki, Ping Fang, Benjamin Alleva, Luis M Franco, John W Belmont, P J Hastings, James R Lupski. Nat Genet 2013
90
17

The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.
Philip M Boone, Bo Yuan, Ian M Campbell, Jennifer C Scull, Marjorie A Withers, Brett C Baggett, Christine R Beck, Christine J Shaw, Pawel Stankiewicz, Paolo Moretti,[...]. Am J Hum Genet 2014
60
17

Zbtb20 defines a hippocampal neuronal identity through direct repression of genes that control projection neuron development in the isocortex.
Jakob V Nielsen, Mads Thomassen, Kjeld Møllgård, Jens Noraberg, Niels A Jensen. Cereb Cortex 2014
31
13

Zinc finger protein Zbtb20 is essential for postnatal survival and glucose homeostasis.
Andrew P R Sutherland, Hai Zhang, Ye Zhang, Monia Michaud, Zhifang Xie, Mary-Elizabeth Patti, Michael J Grusby, Weiping J Zhang. Mol Cell Biol 2009
55
13


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
820
13

Mechanisms for recurrent and complex human genomic rearrangements.
Pengfei Liu, Claudia M B Carvalho, P J Hastings, James R Lupski. Curr Opin Genet Dev 2012
216
13

Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
Lisenka E L M Vissers, Samarth S Bhatt, Irene M Janssen, Zhilian Xia, Seema R Lalani, Rolph Pfundt, Katarzyna Derwinska, Bert B A de Vries, Christian Gilissen, Alexander Hoischen,[...]. Hum Mol Genet 2009
121
13

Detection of clinically relevant exonic copy-number changes by array CGH.
Philip M Boone, Carlos A Bacino, Chad A Shaw, Patricia A Eng, Patricia M Hixson, Amber N Pursley, Sung-Hae L Kang, Yaping Yang, Joanna Wiszniewska, Beata A Nowakowska,[...]. Hum Mutat 2010
185
13

Recent segmental duplications in the human genome.
Jeffrey A Bailey, Zhiping Gu, Royden A Clark, Knut Reinert, Rhea V Samonte, Stuart Schwartz, Mark D Adams, Eugene W Myers, Peter W Li, Evan E Eichler. Science 2002
935
13

The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.
Feng Zhang, Mehrdad Khajavi, Anne M Connolly, Charles F Towne, Sat Dev Batish, James R Lupski. Nat Genet 2009
300
13

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.
Yue Luo, Karen E Hermetz, Jodi M Jackson, Jennifer G Mulle, Anne Dodd, Karen D Tsuchiya, Blake C Ballif, Lisa G Shaffer, Jannine D Cody, David H Ledbetter,[...]. Hum Mol Genet 2011
29
13

Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes.
Malene B Rasmussen, Jakob V Nielsen, Charles M Lourenço, Joana B Melo, Christina Halgren, Camila V L Geraldi, Wilson Marques, Guilherme R Rodrigues, Mads Thomassen, Mads Bak,[...]. J Med Genet 2014
22
18

A high-density SNP genome-wide linkage scan in a large autism extended pedigree.
K Allen-Brady, J Miller, N Matsunami, J Stevens, H Block, M Farley, L Krasny, C Pingree, J Lainhart, M Leppert,[...]. Mol Psychiatry 2009
58
10

Resistance to change and vulnerability to stress: autistic-like features of GAP43-deficient mice.
K J Zaccaria, D C Lagace, A J Eisch, J S McCasland. Genes Brain Behav 2010
32
10

Microduplication 3q13.2q13.31 identified in a male with dysmorphic features and multiple congenital anomalies.
Emmanouil Karavitakis, Sofia Kitsiou-Tzeli, Athena Xaidara, Konstantina Kosma, Periklis Makrythanasis, Eleni Apazidou, Emmanuel Kanavakis, Maria Tzetis. Am J Med Genet A 2014
4
75


Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Anath C Lionel, Jennifer Crosbie, Nicole Barbosa, Tara Goodale, Bhooma Thiruvahindrapuram, Jessica Rickaby, Matthew Gazzellone, Andrew R Carson, Jennifer L Howe, Zhuozhi Wang,[...]. Sci Transl Med 2011
225
10

Hippocampus-like corticoneurogenesis induced by two isoforms of the BTB-zinc finger gene Zbtb20 in mice.
Jakob V Nielsen, Flemming H Nielsen, Rola Ismail, Jens Noraberg, Niels A Jensen. Development 2007
49
10

Adult expression of a 3q13.31 microdeletion.
Chelsea Lowther, Gregory Costain, Rebecca Melvin, Dimitri J Stavropoulos, Anath C Lionel, Christian R Marshall, Stephen W Scherer, Anne S Bassett. Mol Cytogenet 2014
9
33


Patient with novel interstitial deletion of chromosome 3q13.1q13.3 and agenesis of the corpus callosum.
Amy Lawson-Yuen, Sue Ann Berend, Janet S Soul, Mira Irons. Clin Dysmorphol 2006
17
17


HERVd: the Human Endogenous RetroViruses Database: update.
Jan Paces, Adam Pavlícek, Radek Zika, Vladimir V Kapitonov, Jerzy Jurka, Václav Paces. Nucleic Acids Res 2004
40
10

Genome architecture, rearrangements and genomic disorders.
Paweł Stankiewicz, James R Lupski. Trends Genet 2002
627
10

Alu repeats and human genomic diversity.
Mark A Batzer, Prescott L Deininger. Nat Rev Genet 2002
927
10

Clinical significance of de novo and inherited copy-number variation.
Anneke T Vulto-van Silfhout, Jayne Y Hehir-Kwa, Bregje W M van Bon, Janneke H M Schuurs-Hoeijmakers, Stephen Meader, Claudia J M Hellebrekers, Ilse J M Thoonen, Arjan P M de Brouwer, Han G Brunner, Caleb Webber,[...]. Hum Mutat 2013
79
10

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
290
10

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
Angela L Duker, Blake C Ballif, Erawati V Bawle, Richard E Person, Sangeetha Mahadevan, Sarah Alliman, Regina Thompson, Ryan Traylor, Bassem A Bejjani, Lisa G Shaffer,[...]. Eur J Hum Genet 2010
216
10

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.
Jayne Y Hehir-Kwa, Benjamín Rodríguez-Santiago, Lisenka E Vissers, Nicole de Leeuw, Rolph Pfundt, Jan K Buitelaar, Luis A Pérez-Jurado, Joris A Veltman. J Med Genet 2011
75
10

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
385
10


Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients.
L T Reiter, P J Hastings, E Nelis, P De Jonghe, C Van Broeckhoven, J R Lupski. Am J Hum Genet 1998
128
10

A common sequence motif associated with recombination hot spots and genome instability in humans.
Simon Myers, Colin Freeman, Adam Auton, Peter Donnelly, Gil McVean. Nat Genet 2008
309
10

Structural variation in the human genome and its role in disease.
Paweł Stankiewicz, James R Lupski. Annu Rev Med 2010
676
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.