A citation-based method for searching scientific literature

Stela Z Berisha, Shashi Shetty, Thomas W Prior, Anna L Mitchell. Birth Defects Res 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Duplication of 7q36.3 encompassing the Sonic Hedgehog (SHH) gene is associated with congenital muscular hypertrophy.
L Kroeldrup, S Kjaergaard, M Kirchhoff, K Kock, C Brasch-Andersen, M Kibaek, L B Ousager. Eur J Med Genet 2012
8
100

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein.
Yongsu Jeong, Federico Coluccio Leskow, Kenia El-Jaick, Erich Roessler, Maximilian Muenke, Anastasia Yocum, Christele Dubourg, Xue Li, Xin Geng, Guillermo Oliver,[...]. Nat Genet 2008
127
100

Disruption of autoregulatory feedback by a mutation in a remote, ultraconserved PAX6 enhancer causes aniridia.
Shipra Bhatia, Hemant Bengani, Margaret Fish, Alison Brown, Maria Teresa Divizia, Riccardo de Marco, Guiseppe Damante, Robert Grainger, Veronica van Heyningen, Dirk A Kleinjan. Am J Hum Genet 2013
93
100


The evolution of lineage-specific regulatory activities in the human embryonic limb.
Justin Cotney, Jing Leng, Jun Yin, Steven K Reilly, Laura E DeMare, Deena Emera, Albert E Ayoub, Pasko Rakic, James P Noonan. Cell 2013
124
100

Retinoic acid controls expression of tissue remodeling genes Hmgn1 and Fgf18 at the digit-interdigit junction.
Xianling Zhao, Thomas Brade, Thomas J Cunningham, Gregg Duester. Dev Dyn 2010
28
100

Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning.
Byoung-Il Bae, Ian Tietjen, Kutay D Atabay, Gilad D Evrony, Matthew B Johnson, Ebenezer Asare, Peter P Wang, Ayako Y Murayama, Kiho Im, Steven N Lisgo,[...]. Science 2014
121
100

Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome.
S Lohan, M Spielmann, S C Doelken, R Flöttmann, F Muhammad, S M Baig, M Wajid, W Hülsemann, R Habenicht, K W Kjaer,[...]. Clin Genet 2014
36
100

Deficiency in the secreted protein Semaphorin3d causes abnormal parathyroid development in mice.
Anamika Singh, Masum M Mia, Dasan Mary Cibi, Ashutosh Kumar Arya, Sanjay Kumar Bhadada, Manvendra K Singh. J Biol Chem 2019
3
100

Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactyly.
Mio Aerden, Marijke Bauters, Kris Van Den Bogaert, Joris R Vermeesch, Maureen Holvoet, Frank Plasschaert, Koenraad Devriendt. Eur J Med Genet 2020
2
100

HMGB factors are required for posterior digit development through integrating signaling pathway activities.
Junji Itou, Noboru Taniguchi, Isao Oishi, Hiroko Kawakami, Martin Lotz, Yasuhiko Kawakami. Dev Dyn 2011
20
100

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.
M Muenke, U Schell, A Hehr, N H Robin, H W Losken, A Schinzel, L J Pulleyn, P Rutland, W Reardon, S Malcolm. Nat Genet 1994
488
100

Active site remodelling accompanies thioester bond formation in the SUMO E1.
Shaun K Olsen, Allan D Capili, Xuequan Lu, Derek S Tan, Christopher D Lima. Nature 2010
139
100

Advancements in Next-Generation Sequencing.
Shawn E Levy, Richard M Myers. Annu Rev Genomics Hum Genet 2016
185
100

Topological domains in mammalian genomes identified by analysis of chromatin interactions.
Jesse R Dixon, Siddarth Selvaraj, Feng Yue, Audrey Kim, Yan Li, Yin Shen, Ming Hu, Jun S Liu, Bing Ren. Nature 2012
100

19q13.11 microdeletion: Clinical features overlapping ectrodactyly ectodermal dysplasia-clefting syndrome phenotype.
Kikue Terada Abe, Isabela M P O Rizzo, Ana L V Coelho, Nilo Sakai, Daniel R Carvalho, Carlos E Speck-Martins. Clin Case Rep 2018
5
100

Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.
Michael N Weedon, Ines Cebola, Ann-Marie Patch, Sarah E Flanagan, Elisa De Franco, Richard Caswell, Santiago A Rodríguez-Seguí, Charles Shaw-Smith, Candy H-H Cho, Hana Lango Allen,[...]. Nat Genet 2014
152
100

The single-cell transcriptional landscape of mammalian organogenesis.
Junyue Cao, Malte Spielmann, Xiaojie Qiu, Xingfan Huang, Daniel M Ibrahim, Andrew J Hill, Fan Zhang, Stefan Mundlos, Lena Christiansen, Frank J Steemers,[...]. Nature 2019
396
100

Noncoding copy-number variations are associated with congenital limb malformation.
Ricarda Flöttmann, Bjørt K Kragesteen, Sinje Geuer, Magdalena Socha, Lila Allou, Anna Sowińska-Seidler, Laure Bosquillon de Jarcy, Johannes Wagner, Aleksander Jamsheer, Barbara Oehl-Jaschkowitz,[...]. Genet Med 2018
18
100

Duplication of 10q24 locus: broadening the clinical and radiological spectrum.
Muriel Holder-Espinasse, Aleksander Jamsheer, Fabienne Escande, Joris Andrieux, Florence Petit, Anna Sowinska-Seidler, Magdalena Socha, Anna Jakubiuk-Tomaszuk, Marion Gerard, Michèle Mathieu-Dramard,[...]. Eur J Hum Genet 2019
2
100

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.
Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, Claudia M B Carvalho, Malin Kvarnung, Giedre Grigelioniene, Britt-Marie Anderlid, Olof Bjerin, Peter Gustavsson, Anna Hammarsjö,[...]. Genome Med 2019
31
100

VarFish: comprehensive DNA variant analysis for diagnostics and research.
Manuel Holtgrewe, Oliver Stolpe, Mikko Nieminen, Stefan Mundlos, Alexej Knaus, Uwe Kornak, Dominik Seelow, Lara Segebrecht, Malte Spielmann, Björn Fischer-Zirnsak,[...]. Nucleic Acids Res 2020
9
100

A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
Xavier J de Mollerat, Fiorella Gurrieri, Chad T Morgan, Eugenio Sangiorgi, David B Everman, Paola Gaspari, Jeanne Amiel, Michael J Bamshad, Robert Lyle, Jean-Louis Blouin,[...]. Hum Mol Genet 2003
80
100


FGFR2 mutation in a patient without typical features of Pfeiffer syndrome--The emerging role of combined NGS and phenotype based strategies.
Ricarda Flöttmann, Alexej Knaus, Tomasz Zemojtel, Peter N Robinson, Stefan Mundlos, Denise Horn, Malte Spielmann. Eur J Med Genet 2015
6
100

Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2).
Kaori Yamoto, Hirotomo Saitsu, Gen Nishimura, Rika Kosaki, Shinichiro Takayama, Nobuhiko Haga, Hidefumi Tonoki, Akihisa Okumura, Emiko Horii, Nobuhiko Okamoto,[...]. Eur J Hum Genet 2019
4
100

Role of the acidic tail of high mobility group protein B1 (HMGB1) in protein stability and DNA bending.
Fabricio S Belgrano, Isabel C de Abreu da Silva, Francisco M Bastos de Oliveira, Marcelo R Fantappié, Ronaldo Mohana-Borges. PLoS One 2013
30
100

Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion.
Eva Klopocki, Silke Lohan, Sandra C Doelken, Sigmar Stricker, Charlotte W Ockeloen, Renata Soares Thiele de Aguiar, Karina Lezirovitz, Regina Celia Mingroni Netto, Aleksander Jamsheer, Hitesh Shah,[...]. J Med Genet 2012
57
100

Joining the fingers: a HOXD13 Story.
Nathalie Brison, Philippe Debeer, Przemko Tylzanowski. Dev Dyn 2014
12
100

Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patients.
Shimul Chowdhury, Anne M Bandholz, Sandhya Parkash, Sarah Dyack, Andrea L Rideout, Kathleen A Leppig, Heidi Thiese, Patricia G Wheeler, Marilyn Tsang, Blake C Ballif,[...]. Am J Med Genet A 2014
15
100


ChIP-seq accurately predicts tissue-specific activity of enhancers.
Axel Visel, Matthew J Blow, Zirong Li, Tao Zhang, Jennifer A Akiyama, Amy Holt, Ingrid Plajzer-Frick, Malak Shoukry, Crystal Wright, Feng Chen,[...]. Nature 2009
100

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
100

HOXA13 regulates Aldh1a2 expression in the autopod to facilitate interdigital programmed cell death.
Siming Shou, Hanqian L Carlson, Wilma D Perez, H Scott Stadler. Dev Dyn 2013
10
100

Whole-genome sequencing of patients with rare diseases in a national health system.
Ernest Turro, William J Astle, Karyn Megy, Stefan Gräf, Daniel Greene, Olga Shamardina, Hana Lango Allen, Alba Sanchis-Juan, Mattia Frontini, Chantal Thys,[...]. Nature 2020
70
100

Genome sequencing identifies major causes of severe intellectual disability.
Christian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W M van Bon, Marjolein H Willemsen, Michael Kwint, Irene M Janssen, Alexander Hoischen, Annette Schenck,[...]. Nature 2014
619
100

A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly.
Laura A Lettice, Simon J H Heaney, Lorna A Purdie, Li Li, Philippe de Beer, Ben A Oostra, Debbie Goode, Greg Elgar, Robert E Hill, Esther de Graaff. Hum Mol Genet 2003
710
100

Disruption of the SEMA3D gene in a patient with congenital heart defects.
Marta Sanchez-Castro, Olivier Pichon, Annaig Briand, Damien Poulain, Véronique Gournay, Albert David, Cédric Le Caignec. Hum Mutat 2015
18
100

The acidic tail of HMGB1 regulates its secondary structure and conformational flexibility: A circular dichroism and molecular dynamics simulation study.
Wresti L Anggayasti, Kenta Ogino, Eiji Yamamoto, Erik Helmerhorst, Kenji Yasuoka, Ricardo L Mancera. Comput Struct Biotechnol J 2020
4
100


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.