A citation-based method for searching scientific literature

Xi Wang, Lin Han, Xiao-Yan Wang, Jian-Hong Wang, Xiao-Meng Li, Chun-Hua Jin, Lin Wang. Front Genet 2020
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Hypothesis: lobe A (COG1-4)-CDG causes a more severe phenotype than lobe B (COG5-8)-CDG.
Hanneke A Haijes, Jaak Jaeken, François Foulquier, Peter M van Hasselt. J Med Genet 2018
13
55

Key features and clinical variability of COG6-CDG.
Daisy Rymen, Julia Winter, Peter M Van Hasselt, Jaak Jaeken, Cigdem Kasapkara, Gulden Gokçay, Hanneke Haijes, Philippe Goyens, Aysegul Tokatli, Christian Thiel,[...]. Mol Genet Metab 2015
38
55

Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation.
H Kodera, N Ando, I Yuasa, Y Wada, Y Tsurusaki, M Nakashima, N Miyake, S Saitoh, N Matsumoto, H Saitsu. Clin Genet 2015
39
44

A novel syndrome of hypohidrosis and intellectual disability is linked to COG6 deficiency.
Ranad Shaheen, Shinu Ansari, Muneera J Alshammari, Hisham Alkhalidi, Hadeel Alrukban, Wafaa Eyaid, Fowzan S Alkuraya. J Med Genet 2013
35
44

Compound heterozygous variants of the COG6 gene in a Chinese patient with deficiency of subunit 6 of the conserved oligomeric Golgi complex (COG6-CDG).
Guoqiang Li, Yufei Xu, Xuyun Hu, Niu Li, Ruen Yao, Tingting Yu, Xiumin Wang, Weiwei Guo, Jian Wang. Eur J Med Genet 2019
11
44

COG5-CDG with a Mild Neurohepatic Presentation.
C W Fung, G Matthijs, L Sturiale, D Garozzo, K Y Wong, R Wong, V Wong, J Jaeken. JIMD Rep 2012
27
44

Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.
Jürgen Lübbehusen, Christian Thiel, Nina Rind, Daniel Ungar, Berthil H C M T Prinsen, Tom J de Koning, Peter M van Hasselt, Christian Körner. Hum Mol Genet 2010
78
44

Maintaining order: COG complex controls Golgi trafficking, processing, and sorting.
Jessica B Blackburn, Zinia D'Souza, Vladimir V Lupashin. FEBS Lett 2019
30
44

Deficiency of Subunit 6 of the Conserved Oligomeric Golgi Complex (COG6-CDG): Second Patient, Different Phenotype.
S Huybrechts, C De Laet, P Bontems, S Rooze, H Souayah, Y Sznajer, L Sturiale, D Garozzo, G Matthijs, A Ferster,[...]. JIMD Rep 2012
29
44

Congenital disorders of glycosylation (CDG): Quo vadis?
Romain Péanne, Pascale de Lonlay, François Foulquier, Uwe Kornak, Dirk J Lefeber, Eva Morava, Belén Pérez, Nathalie Seta, Christian Thiel, Emile Van Schaftingen,[...]. Eur J Med Genet 2018
130
33

A new mutation in COG7 extends the spectrum of COG subunit deficiencies.
Renate Zeevaert, François Foulquier, David Cheillan, Isabelle Cloix, Nathalie Guffon, Luisella Sturiale, Domenico Garozzo, Gert Matthijs, Jaak Jaeken. Eur J Med Genet 2009
31
33

Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.
François Foulquier, Eliza Vasile, Els Schollen, Nico Callewaert, Tim Raemaekers, Dulce Quelhas, Jaak Jaeken, Philippa Mills, Bryan Winchester, Monty Krieger,[...]. Proc Natl Acad Sci U S A 2006
145
33

Golgi function and dysfunction in the first COG4-deficient CDG type II patient.
Ellen Reynders, François Foulquier, Elisa Leão Teles, Dulce Quelhas, Willy Morelle, Cathérine Rabouille, Wim Annaert, Gert Matthijs. Hum Mol Genet 2009
105
33

Further delineation of COG8-CDG: A case with novel compound heterozygous mutations diagnosed by targeted exome sequencing.
Aram Yang, Sung Yoon Cho, Ja-Hyun Jang, Jinsup Kim, Sook Za Kim, Beom Hee Lee, Han-Wook Yoo, Dong-Kyu Jin. Clin Chim Acta 2017
9
33

Secondary Hemophagocytic Syndrome Associated with COG6 Gene Defect: Report and Review.
Nouf Althonaian, Abdulrahman Alsultan, Eva Morava, Majid Alfadhel. JIMD Rep 2018
15
33

Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation.
Patricie Paesold-Burda, Charlotte Maag, Heinz Troxler, François Foulquier, Peter Kleinert, Siegrun Schnabel, Matthias Baumgartner, Thierry Hennet. Hum Mol Genet 2009
86
33

Identification of the first COG-CDG patient of Indian origin.
Bobby G Ng, Vandana Sharma, Liangwu Sun, Eva Loh, Wanjin Hong, Stacey K H Tay, Hudson H Freeze. Mol Genet Metab 2011
35
33

Subunit architecture of the conserved oligomeric Golgi complex.
Daniel Ungar, Toshihiko Oka, Eliza Vasile, Monty Krieger, Frederick M Hughson. J Biol Chem 2005
79
33

Novel compound heterozygous COG5 mutations in a Chinese male patient with severe clinical symptoms and type IIi congenital disorder of glycosylation: A case report.
Shaowei Yin, Liying Gong, Hao Qiu, Yan Zhao, Yan Zhang, Caixia Liu, Hongkun Jiang, Yan Mao, Ling-Yin Kong, Bo Liang,[...]. Exp Ther Med 2019
4
75

A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.
Carlos R Ferreira, Zhi-Jie Xia, Aurélie Clément, David A Parry, Mariska Davids, Fulya Taylan, Prashant Sharma, Coleman T Turgeon, Bernardo Blanco-Sánchez, Bobby G Ng,[...]. Am J Hum Genet 2018
38
33

The first case of antenatal presentation in COG8-congenital disorder of glycosylation with a novel splice site mutation and an extended phenotype.
Veronica Arora, Ratna Dua Puri, Pratibha Bhai, Nidhish Sharma, Sunita Bijarnia-Mahay, Nandita Dimri, Ashok Baijal, Renu Saxena, Ishwar Verma. Am J Med Genet A 2019
12
33

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
33


Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects.
Willy Morelle, Sven Potelle, Peter Witters, Sunnie Wong, Leslie Climer, Vladimir Lupashin, Gert Matthijs, Therese Gadomski, Jaak Jaeken, David Cassiman,[...]. J Clin Endocrinol Metab 2017
46
22

A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation.
François Foulquier, Daniel Ungar, Ellen Reynders, Renate Zeevaert, Philippa Mills, Maria Teresa García-Silva, Paz Briones, Bryan Winchester, Willy Morelle, Monty Krieger,[...]. Hum Mol Genet 2007
101
22

Interaction of Golgin-84 with the COG complex mediates the intra-Golgi retrograde transport.
Miwa Sohda, Yoshio Misumi, Akitsugu Yamamoto, Nobuhiro Nakamura, Shigenori Ogata, Shotaro Sakisaka, Shinichi Hirose, Yukio Ikehara, Kimimitsu Oda. Traffic 2010
53
22

How to find and diagnose a CDG due to defective N-glycosylation.
Dirk J Lefeber, Eva Morava, Jaak Jaeken. J Inherit Metab Dis 2011
70
22


Oral D-galactose supplementation in PGM1-CDG.
Sunnie Yan-Wai Wong, Therese Gadomski, Monique van Scherpenzeel, Tomas Honzik, Hana Hansikova, Katja S Brocke Holmefjord, Marit Mork, Francis Bowling, Jolanta Sykut-Cegielska, Dieter Koch,[...]. Genet Med 2017
37
22


A Mild Form of COG5 Defect Showing Early-Childhood-Onset Friedreich's-Ataxia-Like Phenotypes with Isolated Cerebellar Atrophy.
Young Ok Kim, Misun Yun, Jae Ho Jeong, Seong Min Choi, Seul Kee Kim, Woong Yoon, Chungoo Park, Yeongjin Hong, Young Jong Woo. J Korean Med Sci 2017
9
22

The interaction of two tethering factors, p115 and COG complex, is required for Golgi integrity.
Miwa Sohda, Yoshio Misumi, Shin-Ichiro Yoshimura, Nobuhiro Nakamura, Takami Fusano, Shigenori Ogata, Shotaro Sakisaka, Yukio Ikehara. Traffic 2007
57
22

Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder.
Xiaohua Wu, Richard A Steet, Ognian Bohorov, Jaap Bakker, John Newell, Monty Krieger, Leo Spaapen, Stuart Kornfeld, Hudson H Freeze. Nat Med 2004
237
22

Defects in COG-Mediated Golgi Trafficking Alter Endo-Lysosomal System in Human Cells.
Zinia D'Souza, Jessica Bailey Blackburn, Tetyana Kudlyk, Irina D Pokrovskaya, Vladimir V Lupashin. Front Cell Dev Biol 2019
12
22

Multipronged interaction of the COG complex with intracellular membranes.
Rose Willett, Irina Pokrovskaya, Tetyana Kudlyk, Vladimir Lupashin. Cell Logist 2014
17
22



Genetic polymorphisms of hspa1b and hspa1l in infertile men.
Halil Ciftci, Bulent Celepkolo, Fuat Dilmec, Mete Köksal, Ercan Yeni, Ismail Yagmur, Kemal Gümüs. J Pak Med Assoc 2015
5
40

The mechanisms of vesicle budding and fusion.
Juan S Bonifacino, Benjamin S Glick. Cell 2004
22

COG lobe B sub-complex engages v-SNARE GS15 and functions via regulated interaction with lobe A sub-complex.
Rose Willett, Jessica Bailey Blackburn, Leslie Climer, Irina Pokrovskaya, Tetyana Kudlyk, Wei Wang, Vladimir Lupashin. Sci Rep 2016
19
22

A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia.
Eva Morava, Renate Zeevaert, Eckhard Korsch, Karin Huijben, Suzan Wopereis, Gert Matthijs, Kathelijn Keymolen, Dirk J Lefeber, Linda De Meirleir, Ron A Wevers. Eur J Hum Genet 2007
74
22

More than just sugars: Conserved oligomeric Golgi complex deficiency causes glycosylation-independent cellular defects.
Jessica B Blackburn, Tetyana Kudlyk, Irina Pokrovskaya, Vladimir V Lupashin. Traffic 2018
17
22


COG8 deficiency causes new congenital disorder of glycosylation type IIh.
Christian Kranz, Bobby G Ng, Liangwu Sun, Vandana Sharma, Erik A Eklund, Yoshiaki Miura, Daniel Ungar, Vladimir Lupashin, R Dennis Winkel, John F Cipollo,[...]. Hum Mol Genet 2007
91
22

Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function.
Daniel Ungar, Toshihiko Oka, Elizabeth E Brittle, Eliza Vasile, Vladimir V Lupashin, Jon E Chatterton, John E Heuser, Monty Krieger, M Gerard Waters. J Cell Biol 2002
215
22

COG Complex Complexities: Detailed Characterization of a Complete Set of HEK293T Cells Lacking Individual COG Subunits.
Jessica Bailey Blackburn, Irina Pokrovskaya, Peter Fisher, Daniel Ungar, Vladimir V Lupashin. Front Cell Dev Biol 2016
37
22

The Golgi puppet master: COG complex at center stage of membrane trafficking interactions.
Rose Willett, Daniel Ungar, Vladimir Lupashin. Histochem Cell Biol 2013
82
22


Conserved oligomeric Golgi complex specifically regulates the maintenance of Golgi glycosylation machinery.
Irina D Pokrovskaya, Rose Willett, Richard D Smith, Willy Morelle, Tetyana Kudlyk, Vladimir V Lupashin. Glycobiology 2011
72
22

Molecular architecture of the complete COG tethering complex.
Jun Yong Ha, Hui-Ting Chou, Daniel Ungar, Calvin K Yip, Thomas Walz, Frederick M Hughson. Nat Struct Mol Biol 2016
23
22


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.