A citation-based method for searching scientific literature

Loredana Poeta, Denise Drongitis, Lucia Verrillo, Maria Giuseppina Miano. Genes (Basel) 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


A reliable strategy for single-cell RNA sequencing analysis using cryoconserved primary cortical cells.
Lucia Verrillo, Eleonora Mangano, Denise Drongitis, Ivan Merelli, Francesca Pischedda, Giovanni Piccoli, Clarissa Consolandi, Roberta Bordoni, Maria Giuseppina Miano. J Neurosci Methods 2021
2
100

A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX.
Loredana Poeta, Francesca Fusco, Denise Drongitis, Cheryl Shoubridge, Genesia Manganelli, Stefania Filosa, Mariateresa Paciolla, Monica Courtney, Patrick Collombat, Maria Brigida Lioi,[...]. Am J Hum Genet 2013
28
50

ARX spectrum disorders: making inroads into the molecular pathology.
Cheryl Shoubridge, Tod Fullston, Jozef Gécz. Hum Mutat 2010
113
50

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.
Mitsuhiro Kato, Soma Das, Kristin Petras, Kunio Kitamura, Ken-Ichirou Morohashi, Diane N Abuelo, Mason Barr, Dominique Bonneau, Angela F Brady, Nancy J Carpenter,[...]. Hum Mutat 2004
213
50

Differential effects of a polyalanine tract expansion in Arx on neural development and gene expression.
MacLean Pancoast Nasrallah, Ginam Cho, Jacqueline C Simonet, Mary E Putt, Kunio Kitamura, Jeffrey A Golden. Hum Mol Genet 2012
35
50

Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders.
Loredana Poeta, Agnese Padula, Benedetta Attianese, Mariaelena Valentino, Lucia Verrillo, Stefania Filosa, Cheryl Shoubridge, Adriano Barra, Charles E Schwartz, Jesper Christensen,[...]. Hum Mol Genet 2019
10
50

Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in the ARX homeobox gene.
Tessa Mattiske, Kristie Lee, Jozef Gecz, Gaelle Friocourt, Cheryl Shoubridge. Hum Mol Genet 2016
9
50

MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions.
Carmela Laperuta, Letizia Spizzichino, Pio D'Adamo, Jlenia Monfregola, Antonio Maiorino, Angela D'Eustacchio, Valerio Ventruto, Giovanni Neri, Michele D'Urso, Pietro Chiurazzi,[...]. BMC Med Genet 2007
22
50

Integrative analysis of 111 reference human epigenomes.
Anshul Kundaje, Wouter Meuleman, Jason Ernst, Misha Bilenky, Angela Yen, Alireza Heravi-Moussavi, Pouya Kheradpour, Zhizhuo Zhang, Jianrong Wang, Michael J Ziller,[...]. Nature 2015
25

Organization and function of the 3D genome.
Boyan Bonev, Giacomo Cavalli. Nat Rev Genet 2016
426
25

Enhancer biology and enhanceropathies.
Edwin Smith, Ali Shilatifard. Nat Struct Mol Biol 2014
177
25

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
Amy B Wilfert, Arvis Sulovari, Tychele N Turner, Bradley P Coe, Evan E Eichler. Genome Med 2017
67
25

Regulation of chromatin by histone modifications.
Andrew J Bannister, Tony Kouzarides. Cell Res 2011
25

Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence.
Jacqueline K Rainger, Shipra Bhatia, Hemant Bengani, Philippe Gautier, Joe Rainger, Matt Pearson, Morad Ansari, Jayne Crow, Felicity Mehendale, Bozena Palinkasova,[...]. Hum Mol Genet 2014
44
25

Identification of long non-coding RNAs involved in neuronal development and intellectual disability.
Eva D'haene, Eva Z Jacobs, Pieter-Jan Volders, Tim De Meyer, Björn Menten, Sarah Vergult. Sci Rep 2016
38
25

Integration of genome-wide approaches identifies lncRNAs of adult neural stem cells and their progeny in vivo.
Alexander D Ramos, Aaron Diaz, Abhinav Nellore, Ryan N Delgado, Ki-Youb Park, Gabriel Gonzales-Roybal, Michael C Oldham, Jun S Song, Daniel A Lim. Cell Stem Cell 2013
178
25

Regulatory variants of FOXG1 in the context of its topological domain organisation.
Mana M Mehrjouy, Ana Carolina S Fonseca, Nadja Ehmke, Giorgio Paskulin, Antonio Novelli, Francesco Benedicenti, Maria Antonietta Mencarelli, Alessandra Renieri, Tiffany Busa, Chantal Missirian,[...]. Eur J Hum Genet 2018
10
25

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.
Masayo Kagami, Yoichi Sekita, Gen Nishimura, Masahito Irie, Fumiko Kato, Michiyo Okada, Shunji Yamamori, Hiroshi Kishimoto, Masahiro Nakayama, Yukichi Tanaka,[...]. Nat Genet 2008
217
25

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.
P Devanna, X S Chen, J Ho, D Gajewski, S D Smith, A Gialluisi, C Francks, S E Fisher, D F Newbury, S C Vernes. Mol Psychiatry 2018
32
25

Phenotypic subregions within the split-hand/foot malformation 1 locus.
Malene B Rasmussen, Sven Kreiborg, Per Jensen, Mads Bak, Yuan Mang, Marianne Lodahl, Esben Budtz-Jørgensen, Niels Tommerup, Lisbeth Tranebjærg, Nanna D Rendtorff. Hum Genet 2016
11
25

Aberrant expression of long noncoding RNAs in autistic brain.
Mark N Ziats, Owen M Rennert. J Mol Neurosci 2013
141
25

The impact of structural variation on human gene expression.
Colby Chiang, Alexandra J Scott, Joe R Davis, Emily K Tsang, Xin Li, Yungil Kim, Tarik Hadzic, Farhan N Damani, Liron Ganel, Stephen B Montgomery,[...]. Nat Genet 2017
152
25

Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN.
Rochelle L Coulson, Weston T Powell, Dag H Yasui, Gayathri Dileep, James Resnick, Janine M LaSalle. Hum Mol Genet 2018
14
25

A structural variation reference for medical and population genetics.
Ryan L Collins, Harrison Brand, Konrad J Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C Francioli, Amit V Khera, Chelsea Lowther, Laura D Gauthier, Harold Wang,[...]. Nature 2020
210
25

A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.
Linna Zhang, Yue Qin, Xiaohong Gong, Rui Peng, Chunquan Cai, Yufang Zheng, Yasong Du, Hongyan Wang. Transl Psychiatry 2019
5
25

Hi-C Identifies Complex Genomic Rearrangements and TAD-Shuffling in Developmental Diseases.
Uirá Souto Melo, Robert Schöpflin, Rocio Acuna-Hidalgo, Martin Atta Mensah, Björn Fischer-Zirnsak, Manuel Holtgrewe, Marius-Konstantin Klever, Seval Türkmen, Verena Heinrich, Ilina Datkhaeva Pluym,[...]. Am J Hum Genet 2020
36
25

Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-AS.
P Joel Ross, Wen-Bo Zhang, Rebecca S F Mok, Kirill Zaslavsky, Eric Deneault, Lia D'Abate, Deivid C Rodrigues, Ryan K C Yuen, Muhammad Faheem, Marat Mufteev,[...]. Biol Psychiatry 2020
29
25

VISTA Enhancer Browser--a database of tissue-specific human enhancers.
Axel Visel, Simon Minovitsky, Inna Dubchak, Len A Pennacchio. Nucleic Acids Res 2007
647
25


A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens.
Molly Gasperini, Andrew J Hill, José L McFaline-Figueroa, Beth Martin, Seungsoo Kim, Melissa D Zhang, Dana Jackson, Anh Leith, Jacob Schreiber, William S Noble,[...]. Cell 2019
165
25

Chromatin architecture reorganization during stem cell differentiation.
Jesse R Dixon, Inkyung Jung, Siddarth Selvaraj, Yin Shen, Jessica E Antosiewicz-Bourget, Ah Young Lee, Zhen Ye, Audrey Kim, Nisha Rajagopal, Wei Xie,[...]. Nature 2015
849
25

Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development.
Elena Perenthaler, Soheil Yousefi, Eva Niggl, Tahsin Stefan Barakat. Front Cell Neurosci 2019
27
25

Neurobiological functions of transcriptional enhancers.
Alex S Nord, Anne E West. Nat Neurosci 2020
27
25

High-resolution genome-wide functional dissection of transcriptional regulatory regions and nucleotides in human.
Xinchen Wang, Liang He, Sarah M Goggin, Alham Saadat, Li Wang, Nasa Sinnott-Armstrong, Melina Claussnitzer, Manolis Kellis. Nat Commun 2018
45
25

Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma.
Meredith E Protas, Eric Weh, Tim Footz, Jay Kasberger, Scott C Baraban, Alex V Levin, L Jay Katz, Robert Ritch, Michael A Walter, Elena V Semina,[...]. Hum Mol Genet 2017
17
25

Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions.
Darío G Lupiáñez, Katerina Kraft, Verena Heinrich, Peter Krawitz, Francesco Brancati, Eva Klopocki, Denise Horn, Hülya Kayserili, John M Opitz, Renata Laxova,[...]. Cell 2015
25

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.
Joon-Yong An, Kevin Lin, Lingxue Zhu, Donna M Werling, Shan Dong, Harrison Brand, Harold Z Wang, Xuefang Zhao, Grace B Schwartz, Ryan L Collins,[...]. Science 2018
110
25

Towards a comprehensive catalogue of validated and target-linked human enhancers.
Molly Gasperini, Jacob M Tome, Jay Shendure. Nat Rev Genet 2020
95
25

Genome-wide differential expression of synaptic long noncoding RNAs in autism spectrum disorder.
Y Wang, X Zhao, W Ju, M Flory, J Zhong, S Jiang, P Wang, X Dong, X Tao, Q Chen,[...]. Transl Psychiatry 2015
54
25

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
Tychele N Turner, Fereydoun Hormozdiari, Michael H Duyzend, Sarah A McClymont, Paul W Hook, Ivan Iossifov, Archana Raja, Carl Baker, Kendra Hoekzema, Holly A Stessman,[...]. Am J Hum Genet 2016
168
25

The Long Noncoding RNA Pnky Is a Trans-acting Regulator of Cortical Development In Vivo.
Rebecca E Andersen, Sung Jun Hong, Justin J Lim, Miao Cui, Brock A Harpur, Elizabeth Hwang, Ryan N Delgado, Alexander D Ramos, Siyuan John Liu, Benjamin J Blencowe,[...]. Dev Cell 2019
28
25

A Network of Noncoding Regulatory RNAs Acts in the Mammalian Brain.
Benjamin Kleaveland, Charlie Y Shi, Joanna Stefano, David P Bartel. Cell 2018
307
25

The Evf2 Ultraconserved Enhancer lncRNA Functionally and Spatially Organizes Megabase Distant Genes in the Developing Forebrain.
Ivelisse Cajigas, Abhijit Chakraborty, Kelsey R Swyter, Hao Luo, Monique Bastidas, Maximilliano Nigro, Elizabeth R Morris, Sean Chen, Michael J W VanGompel, David Leib,[...]. Mol Cell 2018
31
25


BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells.
Davor Lessel, Christina Gehbauer, Nuria C Bramswig, Caroline Schluth-Bolard, Sathish Venkataramanappa, Koen L I van Gassen, Maja Hempel, Tobias B Haack, Anja Baresic, Casie A Genetti,[...]. Brain 2018
35
25

Enhancer redundancy provides phenotypic robustness in mammalian development.
Marco Osterwalder, Iros Barozzi, Virginie Tissières, Yoko Fukuda-Yuzawa, Brandon J Mannion, Sarah Y Afzal, Elizabeth A Lee, Yiwen Zhu, Ingrid Plajzer-Frick, Catherine S Pickle,[...]. Nature 2018
252
25

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.
H F Sutherland, R Wadey, J M McKie, C Taylor, U Atif, K A Johnstone, S Halford, U J Kim, J Goodship, A Baldini,[...]. Am J Hum Genet 1996
84
25

Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice.
Kenneth R Johnson, Leona H Gagnon, Cong Tian, Chantal M Longo-Guess, Benjamin E Low, Michael V Wiles, Amy E Kiernan. Genetics 2018
12
25

Balanced gene regulation by an embryonic brain ncRNA is critical for adult hippocampal GABA circuitry.
Allison M Bond, Michael J W Vangompel, Evgeny A Sametsky, Mary F Clark, Julie C Savage, John F Disterhoft, Jhumku D Kohtz. Nat Neurosci 2009
278
25

Genomic perspectives of transcriptional regulation in forebrain development.
Alex S Nord, Kartik Pattabiraman, Axel Visel, John L R Rubenstein. Neuron 2015
97
25


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.