A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Histone H3K27ac separates active from poised enhancers and predicts developmental state.
Menno P Creyghton, Albert W Cheng, G Grant Welstead, Tristan Kooistra, Bryce W Carey, Eveline J Steine, Jacob Hanna, Michael A Lodato, Garrett M Frampton, Phillip A Sharp,[...]. Proc Natl Acad Sci U S A 2010
100

FIMO: scanning for occurrences of a given motif.
Charles E Grant, Timothy L Bailey, William Stafford Noble. Bioinformatics 2011
100


Haplotypes encoding the factor VIII 1241 Glu variation, factor VIII levels and the risk of venous thrombosis.
A Yaël Nossent, Jeroen C J Eikenboom, Hans L Vos, Egbert Bakker, Bea C Tanis, Carine J M Doggen, Rogier M Bertina, Frits R Rosendaal. Thromb Haemost 2006
16
100

Factor VIII and factor IX in a twin population. Evidence for a major effect of ABO locus on factor VIII level.
K H Orstavik, P Magnus, H Reisner, K Berg, J B Graham, W Nance. Am J Hum Genet 1985
212
100



Endothelial cell processing and alternatively spliced transcripts of factor VIII: potential implications for coagulation cascades and pulmonary hypertension.
Claire L Shovlin, Gillian Angus, Richard A Manning, Grace N Okoli, Fatima S Govani, Kay Elderfield, Graeme M Birdsey, Inês G Mollet, Michael A Laffan, Francesco A Mauri. PLoS One 2010
27
100

Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.
Weihong Tang, Mary Cushman, David Green, Stephen S Rich, Leslie A Lange, Qiong Yang, Russell P Tracy, Geoffrey H Tofler, Saonli Basu, James G Wilson,[...]. Am J Hematol 2015
12
100

Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Maria Sabater-Lleal, Jennifer E Huffman, Paul S de Vries, Jonathan Marten, Michael A Mastrangelo, Ci Song, Nathan Pankratz, Cavin K Ward-Caviness, Lisa R Yanek, Stella Trompet,[...]. Circulation 2019
33
100

Phenotypic impact of genomic structural variation: insights from and for human disease.
Joachim Weischenfeldt, Orsolya Symmons, François Spitz, Jan O Korbel. Nat Rev Genet 2013
244
100

New Prothrombin Mutation (Arg596Trp, Prothrombin Padua 2) Associated With Venous Thromboembolism.
Cristiana Bulato, Claudia Maria Radu, Elena Campello, Sabrina Gavasso, Luca Spiezia, Daniela Tormene, Paolo Simioni. Arterioscler Thromb Vasc Biol 2016
33
100

AP-1 transcription factor mediates VEGF-induced endothelial cell migration and proliferation.
Jing Jia, Taiyang Ye, Pengfei Cui, Qian Hua, Huiyan Zeng, Dezheng Zhao. Microvasc Res 2016
34
100


Introns: The Functional Benefits of Introns in Genomes.
Bong-Seok Jo, Sun Shim Choi. Genomics Inform 2015
75
100

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification.
Jan P Schouten, Cathal J McElgunn, Raymond Waaijer, Danny Zwijnenburg, Filip Diepvens, Gerard Pals. Nucleic Acids Res 2002
100

Copy number variations of the F8 gene are associated with venous thromboembolism.
Wei Shen, Yi Gu, Rui Zhu, Lan Zhang, Jiwei Zhang, Chunmei Ying. Blood Cells Mol Dis 2013
6
100

Mutation in blood coagulation factor V associated with resistance to activated protein C.
R M Bertina, B P Koeleman, T Koster, F R Rosendaal, R J Dirven, H de Ronde, P A van der Velden, P H Reitsma. Nature 1994
100

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
112
100

The genetics of haemostasis: a twin study.
M de Lange, H Snieder, R A Ariëns, T D Spector, P J Grant. Lancet 2001
224
100

Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis.
T Koster, A D Blann, E Briët, J P Vandenbroucke, F R Rosendaal. Lancet 1995
903
100

High levels of coagulation factor XI as a risk factor for venous thrombosis.
J C Meijers, W L Tekelenburg, B N Bouma, R M Bertina, F R Rosendaal. N Engl J Med 2000
439
100

X-linked thrombophilia with a mutant factor IX (factor IX Padua).
Paolo Simioni, Daniela Tormene, Giulio Tognin, Sabrina Gavasso, Cristiana Bulato, Nicholas P Iacobelli, Jonathan D Finn, Luca Spiezia, Claudia Radu, Valder R Arruda. N Engl J Med 2009
185
100

Aberrant F8 gene intron 1 inversion with concomitant duplication and deletion in a severe hemophilia A patient from Southern Italy.
V Sanna, C Ceglia, M Tarsitano, B Lombardo, A Coppola, F Zarrilli, G Castaldo, G Di Minno. J Thromb Haemost 2013
13
100

A novel prothrombin mutation in two families with prominent thrombophilia--the first cases of antithrombin resistance in a Caucasian population.
V Djordjevic, M Kovac, P Miljic, M Murata, A Takagi, I Pruner, D Francuski, T Kojima, D Radojkovic. J Thromb Haemost 2013
36
100

FVIII expression by its native promoter sustains long-term correction avoiding immune response in hemophilic mice.
Simone Merlin, Rosella Famà, Ester Borroni, Diego Zanolini, Valentina Bruscaggin, Silvia Zucchelli, Antonia Follenzi. Blood Adv 2019
12
100


LUMPY: a probabilistic framework for structural variant discovery.
Ryan M Layer, Colby Chiang, Aaron R Quinlan, Ira M Hall. Genome Biol 2014
535
100


Patterns of expression of factor VIII and von Willebrand factor by endothelial cell subsets in vivo.
Junliang Pan, Thanh Theresa Dinh, Anusha Rajaraman, Mike Lee, Alexander Scholz, Cathrin J Czupalla, Helena Kiefel, Li Zhu, Lijun Xia, John Morser,[...]. Blood 2016
36
100

The role of transcription enhancer factors in cardiovascular biology.
Yi Jin, Angela F Messmer-Blust, Jian Li. Trends Cardiovasc Med 2011
9
100

Thrombosis from a prothrombin mutation conveying antithrombin resistance.
Yuhri Miyawaki, Atsuo Suzuki, Junko Fujita, Asuka Maki, Eriko Okuyama, Moe Murata, Akira Takagi, Takashi Murate, Shinji Kunishima, Michio Sakai,[...]. N Engl J Med 2012
61
100

Complexity and diversity of F8 genetic variations in the 1000 genomes.
J N Li, I G Carrero, J F Dong, F L Yu. J Thromb Haemost 2015
9
100

Novel FV mutation (W1920R, FVNara) associated with serious deep vein thrombosis and more potent APC resistance relative to FVLeiden.
Keiji Nogami, Keiko Shinozawa, Kenichi Ogiwara, Tomoko Matsumoto, Kagehiro Amano, Katsuyuki Fukutake, Midori Shima. Blood 2014
27
100


Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A.
Richard D Bagnall, Naushin Waseem, Peter M Green, Francesco Giannelli. Blood 2002
269
100

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.
D Lakich, H H Kazazian, S E Antonarakis, J Gitschier. Nat Genet 1993
628
100


Genetic determinants of hemostasis phenotypes in Spanish families.
J C Souto, L Almasy, M Borrell, M Garí, E Martínez, J Mateo, W H Stone, J Blangero, J Fontcuberta. Circulation 2000
214
100

Identification and functional characterization of a novel F5 mutation (Ala512Val, FVB onn ) associated with activated protein C resistance.
B Pezeshkpoor, E Castoldi, A Mahler, D Hanel, J Müller, N S Hamedani, A Biswas, J Oldenburg, A Pavlova. J Thromb Haemost 2016
9
100

Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene.
M R Lalloz, R Schwaab, J H McVey, K Michaelides, E G Tuddenham. Br J Haematol 1994
80
100

Human liver sinusoidal endothelial cells but not hepatocytes contain factor VIII.
T Shahani, K Covens, R Lavend'homme, N Jazouli, E Sokal, K Peerlinck, M Jacquemin. J Thromb Haemost 2014
84
100

Intron sequences that stimulate gene expression in Arabidopsis.
Alan B Rose, Amanda Carter, Ian Korf, Noah Kojima. Plant Mol Biol 2016
23
100

Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A.
N Lannoy, C Bandelier, B Grisart, M Reginster, E Ronge-Collard, M Vikkula, C Hermans. Haemophilia 2015
3
100

Detection of large duplications within the factor VIII gene by MLPA.
S Rost, S Löffler, A Pavlova, C R Müller, J Oldenburg. J Thromb Haemost 2008
41
100

Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
Guillemette Antoni, Tiphaine Oudot-Mellakh, Apostolos Dimitromanolakis, Marine Germain, William Cohen, Philip Wells, Mark Lathrop, France Gagnon, Pierre-Emmanuel Morange, David-Alexandre Tregouet. BMC Med Genet 2011
45
100

The transcription factor LSF: a novel oncogene for hepatocellular carcinoma.
Prasanna K Santhekadur, Devaraja Rajasekaran, Ayesha Siddiq, Rachel Gredler, Dong Chen, Scott E Schaus, Ulla Hansen, Paul B Fisher, Devanand Sarkar. Am J Cancer Res 2012
29
100

EnhancerAtlas: a resource for enhancer annotation and analysis in 105 human cell/tissue types.
Tianshun Gao, Bing He, Sheng Liu, Heng Zhu, Kai Tan, Jiang Qian. Bioinformatics 2016
86
100

The role of microhomology in genomic structural variation.
Diego Ottaviani, Magdalena LeCain, Denise Sheer. Trends Genet 2014
92
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.