A citation-based method for searching scientific literature

Laura Gogoll, Katharina Steindl, Pascal Joset, Markus Zweier, Alessandra Baumer, Christina Gerth-Kahlert, Boris Tutschek, Anita Rauch. Am J Med Genet A 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment.
Jillian P Casey, Svein I Støve, Catherine McGorrian, Joseph Galvin, Marina Blenski, Aimee Dunne, Sean Ennis, Francesca Brett, Mary D King, Thomas Arnesen,[...]. Sci Rep 2015
46
100

Proteome-derived peptide libraries allow detailed analysis of the substrate specificities of N(alpha)-acetyltransferases and point to hNaa10p as the post-translational actin N(alpha)-acetyltransferase.
Petra Van Damme, Rune Evjenth, Håvard Foyn, Kimberly Demeyer, Pieter-Jan De Bock, Johan R Lillehaug, Joël Vandekerckhove, Thomas Arnesen, Kris Gevaert. Mol Cell Proteomics 2011
113
100

A novel NAA10 p.(R83H) variant with impaired acetyltransferase activity identified in two boys with ID and microcephaly.
Rasmus Ree, Anni Sofie Geithus, Pernille Mathiesen Tørring, Kristina Pilekær Sørensen, Mads Damkjær, Sally Ann Lynch, Thomas Arnesen. BMC Med Genet 2019
12
100

Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15.
Hanyin Cheng, Leah Gottlieb, Elaine Marchi, Robert Kleyner, Puja Bhardwaj, Alan F Rope, Sarah Rosenheck, Sébastien Moutton, Christophe Philippe, Wafaa Eyaid,[...]. Hum Mol Genet 2019
24
100

NAA10-related syndrome.
Yiyang Wu, Gholson J Lyon. Exp Mol Med 2018
22
100

Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects.
Line M Myklebust, Petra Van Damme, Svein I Støve, Max J Dörfel, Angèle Abboud, Thomas V Kalvik, Cedric Grauffel, Veronique Jonckheere, Yiyang Wu, Jeffrey Swensen,[...]. Hum Mol Genet 2015
70
100

NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant - a case report.
Nina McTiernan, Svein Isungset Støve, Ingvild Aukrust, Marita Torrisen Mårli, Line M Myklebust, Gunnar Houge, Thomas Arnesen. BMC Med Genet 2018
20
100

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency.
Alan F Rope, Kai Wang, Rune Evjenth, Jinchuan Xing, Jennifer J Johnston, Jeffrey J Swensen, W Evan Johnson, Barry Moore, Chad D Huff, Lynne M Bird,[...]. Am J Hum Genet 2011
165
100

De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females.
Bernt Popp, Svein I Støve, Sabine Endele, Line M Myklebust, Juliane Hoyer, Heinrich Sticht, Silvia Azzarello-Burri, Anita Rauch, Thomas Arnesen, André Reis. Eur J Hum Genet 2015
60
100

Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency.
Chloé Saunier, Svein Isungset Støve, Bernt Popp, Bénédicte Gérard, Marina Blenski, Nicholas AhMew, Charlotte de Bie, Paula Goldenberg, Bertrand Isidor, Boris Keren,[...]. Hum Mutat 2016
49
66



NAA10 polyadenylation signal variants cause syndromic microphthalmia.
Jennifer J Johnston, Kathleen A Williamson, Christopher M Chou, Julie C Sapp, Morad Ansari, Heather M Chapman, David N Cooper, Tabib Dabir, Jeffrey N Dudley, Richard J Holt,[...]. J Med Genet 2019
17
66

A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndrome.
Taraneh Esmailpour, Hamidreza Riazifar, Linan Liu, Sandra Donkervoort, Vincent H Huang, Shreshtha Madaan, Bassem M Shoucri, Anke Busch, Jie Wu, Alexander Towbin,[...]. J Med Genet 2014
63
66

A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy.
Svein Isungset Støve, Marina Blenski, Asbjørg Stray-Pedersen, Klaas J Wierenga, Shalini N Jhangiani, Zeynep Coban Akdemir, David Crawford, Nina McTiernan, Line M Myklebust, Gabriela Purcarin,[...]. Eur J Hum Genet 2018
18
66

Severe syndromic ID and skewed X-inactivation in a girl with NAA10 dysfunction and a novel heterozygous de novo NAA10 p.(His16Pro) variant - a case report.
Ingrid Bader, Nina McTiernan, Christine Darbakk, Eugen Boltshauser, Rasmus Ree, Sabine Ebner, Johannes A Mayr, Thomas Arnesen. BMC Med Genet 2020
5
66

Identification and characterization of the human ARD1-NATH protein acetyltransferase complex.
Thomas Arnesen, Dave Anderson, Christian Baldersheim, Michel Lanotte, Jan E Varhaug, Johan R Lillehaug. Biochem J 2005
144
66

NAA10 variant in 38-week-gestation male patient: a case study.
Antara Afrin, Jeremy W Prokop, Adam Underwood, Katie L Uhl, Elizabeth A VanSickle, Roja Baruwal, Morgan Wajda, Surender Rajasekaran, Caleb Bupp. Cold Spring Harb Mol Case Stud 2020
3
66

NAA10 p.(D10G) and NAA10 p.(L11R) Variants Hamper Formation of the NatA N-Terminal Acetyltransferase Complex.
Nina McTiernan, Christine Darbakk, Rasmus Ree, Thomas Arnesen. Int J Mol Sci 2020
2
100

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
66

Clinical Manifestations in a Girl with NAA10-Related Syndrome and Genotype-Phenotype Correlation in Females.
Ilenia Maini, Stefano G Caraffi, Francesca Peluso, Lara Valeri, Davide Nicoli, Steven Laurie, Chiara Baldo, Orsetta Zuffardi, Livia Garavelli. Genes (Basel) 2021
3
66


A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy.
Ayumi Shishido, Naoya Morisada, Kenta Tominaga, Hiroyasu Uemura, Akiko Haruna, Hiroaki Hanafusa, Kandai Nozu, Kazumoto Iijima. Hum Genome Var 2020
1
100

Expression of human NAA11 (ARD1B) gene is tissue-specific and is regulated by DNA methylation.
Alan L Y Pang, Jessica Clark, Wai-Yee Chan, Owen M Rennert. Epigenetics 2011
11
33

N-α-acetyltransferase 10 (NAA10) in development: the role of NAA10.
Mi-Ni Lee, Hyae Yon Kweon, Goo Taeg Oh. Exp Mol Med 2018
14
33

First Things First: Vital Protein Marks by N-Terminal Acetyltransferases.
Henriette Aksnes, Adrian Drazic, Michaël Marie, Thomas Arnesen. Trends Biochem Sci 2016
142
33

Cloning and characterization of hNAT5/hSAN: an evolutionarily conserved component of the NatA protein N-alpha-acetyltransferase complex.
Thomas Arnesen, Dave Anderson, Janniche Torsvik, Helene B Halseth, Jan Erik Varhaug, Johan R Lillehaug. Gene 2006
59
33

The chaperone-like protein HYPK acts together with NatA in cotranslational N-terminal acetylation and prevention of Huntingtin aggregation.
Thomas Arnesen, Kristian K Starheim, Petra Van Damme, Rune Evjenth, Huyen Dinh, Matthew J Betts, Anita Ryningen, Joël Vandekerckhove, Kris Gevaert, Dave Anderson. Mol Cell Biol 2010
92
33

Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.
S Forrester, M J Kovach, N M Reynolds, R Urban, V Kimonis. Am J Med Genet 2001
26
33

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
712
33

The yeast N(alpha)-acetyltransferase NatA is quantitatively anchored to the ribosome and interacts with nascent polypeptides.
Matthias Gautschi, Sören Just, Andrej Mun, Suzanne Ross, Peter Rücknagel, Yves Dubaquié, Ann Ehrenhofer-Murray, Sabine Rospert. Mol Cell Biol 2003
172
33

Clinical Manifestations Associated With the N-Terminal-Acetyltransferase NAA10 Gene Mutation in a Girl: Ogden Syndrome.
Mandeep Sidhu, Lauren Brady, Mark Tarnopolsky, Gabriel M Ronen. Pediatr Neurol 2017
14
33

Structure and mechanism of non-histone protein acetyltransferase enzymes.
David R Friedmann, Ronen Marmorstein. FEBS J 2013
49
33


Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15.
Hanyin Cheng, Leah Gottlieb, Elaine Marchi, Robert Kleyner, Puja Bhardwaj, Alan F Rope, Sarah Rosenheck, Sébastien Moutton, Christophe Philippe, Wafaa Eyaid,[...]. Hum Mol Genet 2020
3
33

X-linked clinical anophthalmos. Localization of the gene to Xq27-Xq28.
C A Graham, R M Redmond, N C Nevin. Ophthalmic Paediatr Genet 1991
36
33

A family with X-linked anophthalmia: exclusion of SOX3 as a candidate gene.
Anne Slavotinek, Stephen S Lee, Steven P Hamilton. Am J Med Genet A 2005
4
33

Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic test.
J Thevenon, Y Duffourd, A Masurel-Paulet, M Lefebvre, F Feillet, S El Chehadeh-Djebbar, J St-Onge, A Steinmetz, F Huet, M Chouchane,[...]. Clin Genet 2016
145
33

A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy.
Ayumi Shishido, Naoya Morisada, Kenta Tominaga, Hiroyasu Uemura, Akiko Haruna, Hiroaki Hanafusa, Kandai Nozu, Kazumoto Iijima. Hum Genome Var 2020
1
100

Protein N-terminal acetyltransferases: when the start matters.
Kristian K Starheim, Kris Gevaert, Thomas Arnesen. Trends Biochem Sci 2012
197
33


NAA10 as a New Prognostic Marker for Cancer Progression.
Sun Myung Kim, Eunyoung Ha, Jinyoung Kim, Chiheum Cho, So-Jin Shin, Ji Hae Seo. Int J Mol Sci 2020
4
33

ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
33

The Role of N-α-acetyltransferase 10 Protein in DNA Methylation and Genomic Imprinting.
Chen-Cheng Lee, Shih-Huan Peng, Li Shen, Chung-Fan Lee, Ting-Huei Du, Ming-Lun Kang, Guo-Liang Xu, Anup K Upadhyay, Xiaodong Cheng, Yu-Ting Yan,[...]. Mol Cell 2017
29
33

hNaa10p contributes to tumorigenesis by facilitating DNMT1-mediated tumor suppressor gene silencing.
Chung-Fan Lee, Derick S-C Ou, Sung-Bau Lee, Liang-Hao Chang, Ruo-Kai Lin, Ying-Shiuan Li, Anup K Upadhyay, Xiaodong Cheng, Yi-Ching Wang, Han-Shui Hsu,[...]. J Clin Invest 2010
83
33

Molecular basis for N-terminal acetylation by the heterodimeric NatA complex.
Glen Liszczak, Jacob M Goldberg, Håvard Foyn, E James Petersson, Thomas Arnesen, Ronen Marmorstein. Nat Struct Mol Biol 2013
106
33


ARD1-mediated Hsp70 acetylation balances stress-induced protein refolding and degradation.
Ji Hae Seo, Ji-Hyeon Park, Eun Ji Lee, Tam Thuy Lu Vo, Hoon Choi, Jun Yong Kim, Jae Kyung Jang, Hee-Jun Wee, Hye Shin Lee, Se Hwan Jang,[...]. Nat Commun 2016
65
33

Arrest defective-1 controls tumor cell behavior by acetylating myosin light chain kinase.
Dong Hoon Shin, Yang-Sook Chun, Kyoung-Hwa Lee, Hyun-Woo Shin, Jong-Wan Park. PLoS One 2009
58
33

Identification and characterization of genes and mutants for an N-terminal acetyltransferase from yeast.
J R Mullen, P S Kayne, R P Moerschell, S Tsunasawa, M Gribskov, M Colavito-Shepanski, M Grunstein, F Sherman, R Sternglanz. EMBO J 1989
274
33


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.