A citation-based method for searching scientific literature

I Quintela, F Barros-Angueira, L Perez-Gay, D Dacruz, M Castro-Gago, A Carracedo, J Eiris-Punal. Rev Neurol 2015
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
87

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
87

Cerebral palsy, epilepsy, and severe intellectual disability in a patient with 3q29 microduplication syndrome.
Alberto Fernández-Jaén, María del Carmen Castellanos, Ana Laura Fernández-Perrone, Daniel Martín Fernández-Mayoralas, Alberto González de la Vega, Beatriz Calleja-Pérez, Ester Corbacho Fernández, Jacobo Albert, María Carmen Sánchez Hombre. Am J Med Genet A 2014
14
75

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
75

[3q29 microduplication syndrome].
F Aleixandre Blanquer, I Manchón Trives, M J Forniés Arnau, L A Alcaraz Mas, N Picó Alfonso, F Galán Sánchez. An Pediatr (Barc) 2011
7
71

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
62

3q29 microduplication syndrome: Description of two new cases and delineation of the minimal critical region.
Elisa Tassano, Sara Uccella, Thea Giacomini, Mariasavina Severino, Laura Siri, Marcella Gherzi, Maria Elena Celle, Simona Porta, Giorgio Gimelli, Patrizia Ronchetto. Eur J Med Genet 2018
6
66

A de novo proximal 3q29 chromosome microduplication in a patient with oculo auriculo vertebral spectrum.
Valentina Guida, Lorenzo Sinibaldi, Mario Pagnoni, Laura Bernardini, Sara Loddo, Katia Margiotti, Maria Cristina Digilio, Maria Teresa Fadda, Bruno Dallapiccola, Giorgio Iannetti,[...]. Am J Med Genet A 2015
16
37

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
37

Whole-genome copy number variation analysis in anophthalmia and microphthalmia.
K F Schilter, L M Reis, A Schneider, T M Bardakjian, O Abdul-Rahman, B A Kozel, H H Zimmerman, U Broeckel, E V Semina. Clin Genet 2013
27
25

Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28.
A J van Essen, K Kok, A van den Berg, B de Jong, F Stellink, A F Bos, H Scheffer, C H Buys. Hum Genet 1991
34
25

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
638
25

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
25

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
25

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
333
25

Single-nucleotide polymorphisms are associated with cognitive decline at Alzheimer's disease conversion within mild cognitive impairment patients.
Eunjee Lee, Kelly S Giovanello, Andrew J Saykin, Fengchang Xie, Dehan Kong, Yue Wang, Liuqing Yang, Joseph G Ibrahim, P Murali Doraiswamy, Hongtu Zhu. Alzheimers Dement (Amst) 2017
16
25

Microarray analysis of the developing cortex.
Mawahib O Semeralul, Paul C Boutros, Olga Likhodi, Allan B Okey, Hubert H M Van Tol, Albert H C Wong. J Neurobiol 2006
36
25

Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome.
Melissa M Murphy, T Lindsey Burrell, Joseph F Cubells, Roberto Antonio España, Michael J Gambello, Katrina C B Goines, Cheryl Klaiman, Longchuan Li, Derek M Novacek, Ava Papetti,[...]. BMC Psychiatry 2018
10
25

3q29 microduplication in a small family with complex metabolic phenotype from Southern Italy.
Andrea Vitale, Giuseppe Labruna, Annamaria Mancini, Andreina Alfieri, Laura Iaffaldano, Carmela Nardelli, Fabrizio Pasanisi, Lucio Pastore, Pasqualina Buono, Barbara Lombardo. Clin Chem Lab Med 2018
2
100

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation.
Patrick Tarpey, Josep Parnau, Matthew Blow, Hayley Woffendin, Graham Bignell, Charles Cox, James Cox, Helen Davies, Sarah Edkins, Simon Holden,[...]. Am J Hum Genet 2004
123
25

The dup(3q) syndrome: report of eight cases and review of the literature.
P Steinbach, W N Adkins, H Caspar, K W Dumars, J Gebauer, E F Gilbert, T Grimm, M Habedank, I Hansmann, J Herrmann,[...]. Am J Med Genet 1981
83
12

Triad of anorectal, sacral, and presacral anomalies.
G Currarino, D Coln, T Votteler. AJR Am J Roentgenol 1981
315
12

Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.
Moritz Meins, Javad Karimzad Hagh, Fritz Gerresheim, Elisabeth Einhoff, Heidi Olschewski, Henning Strehl, Jörg T Epplen. Am J Med Genet A 2005
17
12

Presenilin-1 uses phospholipase D1 as a negative regulator of beta-amyloid formation.
Dongming Cai, William J Netzer, Minghao Zhong, Yixin Lin, Guangwei Du, Michael Frohman, David A Foster, Sangram S Sisodia, Huaxi Xu, Fred S Gorelick,[...]. Proc Natl Acad Sci U S A 2006
84
12

Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.
M Ireland, C English, I Cross, S Lindsay, T Strachan. J Med Genet 1995
44
12

Duplication 3q syndrome: molecular delineation of the critical region.
M S Aqua, P Rizzu, E A Lindsay, L G Shaffer, E H Zackai, J Overhauser, A Baldini. Am J Med Genet 1995
64
12

Ephrin-B3 is a myelin-based inhibitor of neurite outgrowth.
M Douglas Benson, Mario I Romero, Mark E Lush, Q Richard Lu, Mark Henkemeyer, Luis F Parada. Proc Natl Acad Sci U S A 2005
212
12

EphB receptors coordinate migration and proliferation in the intestinal stem cell niche.
Johan Holmberg, Maria Genander, Michael M Halford, Cecilia Annerén, Mariann Sondell, Michael J Chumley, Robert E Silvany, Mark Henkemeyer, Jonas Frisén. Cell 2006
216
12


The guanine nucleotide exchange factor (GEF) Ect2 is an oncogene in human cancer.
Alan P Fields, Verline Justilien. Adv Enzyme Regul 2010
77
12

A case of pure partial duplication 3q in a fetus due to a maternally inherited der(5)ins(5;3)(q33.1;q26.2q27) delineated by FISH.
A S T Lim, T H Lim, P Chia, S Raman, D L Pickering, D H Zaleski, W G Sanger, S L Tien. Prenat Diagn 2004
7
14

Bidirectional signaling mediated by ephrin-B2 and EphB2 controls urorectal development.
Christopher Dravis, Nobuhiko Yokoyama, Michael J Chumley, Chad A Cowan, Robert E Silvany, Jennifer Shay, Linda A Baker, Mark Henkemeyer. Dev Biol 2004
182
12

The synaptic proteins neurexins and neuroligins are widely expressed in the vascular system and contribute to its functions.
Alessia Bottos, Erika Destro, Alberto Rissone, Stefania Graziano, Gabriele Cordara, Barbara Assenzio, Maria Rosaria Cera, Luciana Mascia, Federico Bussolino, Marco Arese. Proc Natl Acad Sci U S A 2009
37
12

Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype.
E Lopez-Rangel, F J Dill, M A Hrynchak, M I Van Allen. Am J Med Genet 1993
19
12

Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3q.
W Rosenfeld, R S Verma, R C Jhaveri, R Estrada, H Evans, H Dosik. Am J Med Genet 1981
24
12

Phenotype analysis impacts testing strategy in patients with Currarino syndrome.
G Cuturilo, J C Hodge, C K Runke, E C Thorland, M A Al-Owain, J W Ellison, D Babovic-Vuksanovic. Clin Genet 2016
8
12

Cornelia de Lange syndrome.
M I Boyle, C Jespersgaard, K Brøndum-Nielsen, A-M Bisgaard, Z Tümer. Clin Genet 2015
80
12

A screen for downstream effectors of Neurogenin2 in the embryonic neocortex.
Pierre Mattar, Olivier Britz, Christine Johannes, Marta Nieto, Lin Ma, Angela Rebeyka, Natalia Klenin, Franck Polleux, François Guillemot, Carol Schuurmans. Dev Biol 2004
80
12

p21-Activated Kinase 2 Regulates Endothelial Development and Function through the Bmk1/Erk5 Pathway.
Maria Radu, Karen Lyle, Klaus P Hoeflich, Olga Villamar-Cruz, Hartmut Koeppen, Jonathan Chernoff. Mol Cell Biol 2015
35
12

A boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies.
Haiyan Zhu, Yali Hu, Ruifang Zhu, Ying Yang, Xiangyu Zhu, Wanjun Wang. Am J Med Genet A 2013
8
12

Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome.
E J Breslau, C Disteche, J G Hall, H Thuline, P Cooper. Am J Med Genet 1981
23
12

New chromosomal dysmorphic syndromes. 3. Partial trisomy 3q.
S Stengel-Rutkowski, J D Murken, V Pilar, B Dutrillaux, A Rodewald, R Goebel, R Bassermann. Eur J Pediatr 1979
31
12

Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature.
Jacques Pantel, Marie Legendre, Sylvie Cabrol, Latifa Hilal, Yassir Hajaji, Séverine Morisset, Sylvie Nivot, Marie-Pierre Vie-Luton, Dominique Grouselle, Marc de Kerdanet,[...]. J Clin Invest 2006
243
12


Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents.
C Rosenberg, J Knijnenburg, E Bakker, A M Vianna-Morgante, W Sloos, P A Otto, M Kriek, K Hansson, A C V Krepischi-Santos, H Fiegler,[...]. J Med Genet 2006
165
12

Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2011
11
12

Duplication 3q(q21----qter) without limb anomalies.
S R Ismail, B G Kousseff, S M Kotb, S F Kholeif. Am J Med Genet 1991
8
12

Pierpont syndrome: a collaborative study.
Emma M M Burkitt Wright, Mohnish Suri, Susan M White, Nicole de Leeuw, Anneke T Vulto-van Silfhout, Fiona Stewart, Shane McKee, Sahar Mansour, Fiona C Connell, Maya Chopra,[...]. Am J Med Genet A 2011
11
12

Murine dishevelled 3 functions in redundant pathways with dishevelled 1 and 2 in normal cardiac outflow tract, cochlea, and neural tube development.
S Leah Etheridge, Saugata Ray, Shuangding Li, Natasha S Hamblet, Nardos Lijam, Michael Tsang, Joy Greer, Natalie Kardos, Jianbo Wang, Daniel J Sussman,[...]. PLoS Genet 2008
227
12

A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.
Laura Rodríguez, Samarth S Bhatt, Mónica García-Castro, Ana Plasencia, Joaquín Fernández-Toral, Elena Abarca, Marcelo de Bello Cioffi, Thomas Liehr. Gene 2014
7
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.