A citation-based method for searching scientific literature

Roberta Milone, Angelo Valetto, Roberta Battini, Veronica Bertini, Giulia Valvo, Giovanni Cioni, Federico Sicca. Eur J Med Genet 2016
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
62

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
50

DUF1220-domain copy number implicated in human brain-size pathology and evolution.
Laura J Dumas, Majesta S O'Bleness, Jonathan M Davis, C Michael Dickens, Nathan Anderson, J G Keeney, Jay Jackson, Megan Sikela, Armin Raznahan, Jay Giedd,[...]. Am J Hum Genet 2012
67
50

Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis.
M Cristina Digilio, Laura Bernardini, Federica Consoli, Francesca R Lepri, M Grazia Giuffrida, Anwar Baban, Cecilia Surace, Rosangela Ferese, Adriano Angioni, Antonio Novelli,[...]. Eur J Med Genet 2013
24
25

Understanding the impact of 1q21.1 copy number variant.
Chansonette Harvard, Emma Strong, Eloi Mercier, Rita Colnaghi, Diana Alcantara, Eva Chow, Sally Martell, Christine Tyson, Monica Hrynchak, Barbara McGillivray,[...]. Orphanet J Rare Dis 2011
39
25


Genetic architecture of reciprocal CNVs.
Christelle Golzio, Nicholas Katsanis. Curr Opin Genet Dev 2013
32
25

Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy.
Jae Seok Lim, Woo-il Kim, Hoon-Chul Kang, Se Hoon Kim, Ah Hyung Park, Eun Kyung Park, Young-Wook Cho, Sangwoo Kim, Ho Min Kim, Jeong A Kim,[...]. Nat Med 2015
239
25

Analysis of TSC cortical tubers by deep sequencing of TSC1, TSC2 and KRAS demonstrates that small second-hit mutations in these genes are rare events.
Wei Qin, Jennifer A Chan, Harry V Vinters, Gary W Mathern, David N Franz, Bruce E Taillon, Pascal Bouffard, David J Kwiatkowski. Brain Pathol 2010
75
25

Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.
Alissa M D'Gama, Ying Geng, Javier A Couto, Beth Martin, Evan A Boyle, Christopher M LaCoursiere, Amer Hossain, Nicole E Hatem, Brenda J Barry, David J Kwiatkowski,[...]. Ann Neurol 2015
145
25

Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5.
Thomas Scerri, Jessica R Riseley, Greta Gillies, Kate Pope, Rosemary Burgess, Simone A Mandelstam, Leanne Dibbens, Chung W Chow, Wirginia Maixner, Anthony Simon Harvey,[...]. Ann Clin Transl Neurol 2015
57
25

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.
Jae Seok Lim, Ramu Gopalappa, Se Hoon Kim, Suresh Ramakrishna, Minji Lee, Woo-Il Kim, Junho Kim, Sang Min Park, Junehawk Lee, Jung-Hwa Oh,[...]. Am J Hum Genet 2017
79
25

The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission.
Ingmar Blümcke, Maria Thom, Eleonora Aronica, Dawna D Armstrong, Harry V Vinters, Andre Palmini, Thomas S Jacques, Giuliano Avanzini, A James Barkovich, Giorgio Battaglia,[...]. Epilepsia 2011
963
25

Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3.
Joe C Sim, Thomas Scerri, Miriam Fanjul-Fernández, Jessica R Riseley, Greta Gillies, Kate Pope, Hanna van Roozendaal, Julian I Heng, Simone A Mandelstam, George McGillivray,[...]. Ann Neurol 2016
70
25

Focal dysplasia of the cerebral cortex in epilepsy.
D C Taylor, M A Falconer, C J Bruton, J A Corsellis. J Neurol Neurosurg Psychiatry 1971
786
25

Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3 gene.
V Conti, M Pantaleo, C Barba, G Baroni, D Mei, A M Buccoliero, S Giglio, F Giordano, S T Baek, J G Gleeson,[...]. Clin Genet 2015
32
25

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
25

Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Raphael Bernier, Kyle J Steinman, Beau Reilly, Arianne Stevens Wallace, Elliott H Sherr, Nicholas Pojman, Heather C Mefford, Jennifer Gerdts, Rachel Earl, Ellen Hanson,[...]. Genet Med 2016
73
25

Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.
Martina Busè, Helenia C Cuttaia, Daniela Palazzo, Marcella V Mazara, Salvatrice A Lauricella, Michela Malacarne, Mauro Pierluigi, Simona Cavani, Maria Piccione. Ital J Pediatr 2017
15
25

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Cornelis A Albers, Dirk S Paul, Harald Schulze, Kathleen Freson, Jonathan C Stephens, Peter A Smethurst, Jennifer D Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone,[...]. Nat Genet 2012
251
25

The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder.
Sanem Yilmaz, Sarenur Gokben, Gul Serdaroglu, Cenk Eraslan, Grazia M S Mancini, Hande Tekin, Hasan Tekgul. Brain Dev 2016
11
12

Zika Virus Infection during Pregnancy in Mice Causes Placental Damage and Fetal Demise.
Jonathan J Miner, Bin Cao, Jennifer Govero, Amber M Smith, Estefania Fernandez, Omar H Cabrera, Charise Garber, Michelle Noll, Robyn S Klein, Kevin K Noguchi,[...]. Cell 2016
518
12


ALDH18A1-related cutis laxa syndrome with cyclic vomiting.
Fumihito Nozaki, Takashi Kusunoki, Nobuhiko Okamoto, Yuto Yamamoto, Fuyuki Miya, Tatsuhiko Tsunoda, Kenjiro Kosaki, Tomohiro Kumada, Minoru Shibata, Tatsuya Fujii. Brain Dev 2016
11
12


Novel RAB3GAP1 compound heterozygous mutations in Japanese siblings with Warburg Micro syndrome.
Miki Asahina, Yusaku Endoh, Tomoko Matsubayashi, Tokiko Fukuda, Tsutomu Ogata. Brain Dev 2016
10
12

Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure.
Xuyu Qian, Ha Nam Nguyen, Mingxi M Song, Christopher Hadiono, Sarah C Ogden, Christy Hammack, Bing Yao, Gregory R Hamersky, Fadi Jacob, Chun Zhong,[...]. Cell 2016
878
12

Zika virus impairs growth in human neurospheres and brain organoids.
Patricia P Garcez, Erick Correia Loiola, Rodrigo Madeiro da Costa, Luiza M Higa, Pablo Trindade, Rodrigo Delvecchio, Juliana Minardi Nascimento, Rodrigo Brindeiro, Amilcar Tanuri, Stevens K Rehen. Science 2016
647
12

Detection and sequencing of Zika virus from amniotic fluid of fetuses with microcephaly in Brazil: a case study.
Guilherme Calvet, Renato S Aguiar, Adriana S O Melo, Simone A Sampaio, Ivano de Filippis, Allison Fabri, Eliane S M Araujo, Patricia C de Sequeira, Marcos C L de Mendonça, Louisi de Oliveira,[...]. Lancet Infect Dis 2016
654
12

The Zika outbreak of the 21st century.
Christopher Chang, Kristina Ortiz, Aftab Ansari, M Eric Gershwin. J Autoimmun 2016
109
12

The Brazilian Zika virus strain causes birth defects in experimental models.
Fernanda R Cugola, Isabella R Fernandes, Fabiele B Russo, Beatriz C Freitas, João L M Dias, Katia P Guimarães, Cecília Benazzato, Nathalia Almeida, Graciela C Pignatari, Sarah Romero,[...]. Nature 2016
738
12

7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly.
Keiko Shimojima, Satoshi Narai, Masami Togawa, Tomotsune Doumoto, Noriko Sangu, Olivier M Vanakker, Anne de Paepe, Matthew Edwards, John Whitehall, Sally Brescianini,[...]. Eur J Med Genet 2016
7
14

Zika virus in the Americas: Early epidemiological and genetic findings.
Nuno Rodrigues Faria, Raimunda do Socorro da Silva Azevedo, Moritz U G Kraemer, Renato Souza, Mariana Sequetin Cunha, Sarah C Hill, Julien Thézé, Michael B Bonsall, Thomas A Bowden, Ilona Rissanen,[...]. Science 2016
621
12

Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation.
Anna Maria Pinto, Laura Bianciardi, Maria Antonietta Mencarelli, Valentina Imperatore, Chiara Di Marco, Simone Furini, Agnese Suppiej, Leonardo Salviati, Romano Tenconi, Francesca Ariani,[...]. Brain Dev 2016
7
14

A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features.
Piero Pavone, Andrea Domenico Praticò, Giulia Gentile, Raffaele Falsaperla, Rosario Iemmolo, Maria Guarnaccia, Sebastiano Cavallaro, Martino Ruggieri. Eur J Med Genet 2016
5
20

A Susceptible Mouse Model for Zika Virus Infection.
Stuart D Dowall, Victoria A Graham, Emma Rayner, Barry Atkinson, Graham Hall, Robert J Watson, Andrew Bosworth, Laura C Bonney, Samantha Kitchen, Roger Hewson. PLoS Negl Trop Dis 2016
211
12

Structure of the thermally stable Zika virus.
Victor A Kostyuchenko, Elisa X Y Lim, Shuijun Zhang, Guntur Fibriansah, Thiam-Seng Ng, Justin S G Ooi, Jian Shi, Shee-Mei Lok. Nature 2016
305
12

Zika Virus Associated with Microcephaly.
Jernej Mlakar, Misa Korva, Nataša Tul, Mara Popović, Mateja Poljšak-Prijatelj, Jerica Mraz, Marko Kolenc, Katarina Resman Rus, Tina Vesnaver Vipotnik, Vesna Fabjan Vodušek,[...]. N Engl J Med 2016
12

Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease.
Jesse Christiansen, John D Dyck, Basil G Elyas, Margaret Lilley, J Stephen Bamforth, Mark Hicks, Kathleen A Sprysak, Robert Tomaszewski, Shelagh M Haase, Leanne M Vicen-Wyhony,[...]. Circ Res 2004
104
12

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.
J M Friedman, Agnes Baross, Allen D Delaney, Adrian Ally, Laura Arbour, Linlea Armstrong, Jennifer Asano, Dione K Bailey, Sarah Barber, Patricia Birch,[...]. Am J Hum Genet 2006
213
12

Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.
P T Goodbourn, J M Bosten, G Bargary, R E Hogg, A J Lawrance-Owen, J D Mollon. Genes Brain Behav 2014
26
12

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
12

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Jillian P Casey, Tiago Magalhaes, Judith M Conroy, Regina Regan, Naisha Shah, Richard Anney, Denis C Shields, Brett S Abrahams, Joana Almeida, Elena Bacchelli,[...]. Hum Genet 2012
122
12

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.
David A Koolen, Rolph Pfundt, Nicole de Leeuw, Jayne Y Hehir-Kwa, Willy M Nillesen, Ineke Neefs, Ine Scheltinga, Erik Sistermans, Dominique Smeets, Han G Brunner,[...]. Hum Mutat 2009
112
12

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
Ramachandran Ramya Devi, Perumalsamy Vijayalakshmi. Mol Vis 2006
64
12

Poly(ADP-ribose)-dependent regulation of DNA repair by the chromatin remodeling enzyme ALC1.
Dragana Ahel, Zuzana Horejsí, Nicola Wiechens, Sophie E Polo, Elisa Garcia-Wilson, Ivan Ahel, Helen Flynn, Mark Skehel, Stephen C West, Stephen P Jackson,[...]. Science 2009
380
12

BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1.
Anna Brunet, Lluís Armengol, Damià Heine, Jordi Rosell, Manel García-Aragonés, Elisabeth Gabau, Xavier Estivill, Miriam Guitart. BMC Med Genet 2009
27
12

A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts.
A Arora, P J Minogue, X Liu, P K Addison, I Russel-Eggitt, A R Webster, D M Hunt, L Ebihara, E C Beyer, V M Berthoud,[...]. J Med Genet 2008
55
12


Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome.
Gemma E Rooney, Alice F Goodwin, Philippe Depeille, Amnon Sharir, Claude M Schofield, Erika Yeh, Jeroen P Roose, Ophir D Klein, Katherine A Rauen, Lauren A Weiss,[...]. J Neurosci 2016
20
12


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.