A citation-based method for searching scientific literature

Akbar Dorgalaleh, Yadolah Farshi, Kamand Haeri, Omid Baradarian Ghanbari, Abbas Ahmadi. Semin Thromb Hemost 2022
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Venous Thromboembolism Risk and Thromboprophylaxis in Pediatric Neurosurgery and Spinal Injury: Current Trends and Literature Review.
Dimitrios Panagopoulos, Ploutarchos Karydakis, Georgios Noutsos, Marios Themistocleous. Semin Thromb Hemost 2022
2
50


Tissue Plasminogen Activator in Central Nervous System Physiology and Pathology: From Synaptic Plasticity to Alzheimer's Disease.
Tamara K Stevenson, Shannon J Moore, Geoffrey G Murphy, Daniel A Lawrence. Semin Thromb Hemost 2022
1
100


Neurocoagulation from a Mechanistic Point of View in the Central Nervous System.
Efrat Shavit-Stein, Shani Berkowitz, Shany Guly Gofrit, Keren Altman, Nitai Weinberg, Nicola Maggio. Semin Thromb Hemost 2022
2
50


New Insights in Coagulation and Fibrinolysis in Patients with Primary Brain Cancer: A Systematic Review.
Anne Winther-Larsen, Birgitte Sandfeld-Paulsen, Anne-Mette Hvas. Semin Thromb Hemost 2022
1
100

Spontaneous subarachnoid haemorrhage.
R Loch Macdonald, Tom A Schweizer. Lancet 2017
415
50


Cerebral Venous Thrombosis.
Anne Hege Aamodt, Thor Håkon Skattør. Semin Thromb Hemost 2022
1
100

Cerebral Venous Thrombosis Developing after COVID-19 Vaccination: VITT, VATT, TTS, and More.
Giuseppe Lippi, Emmanuel J Favaloro. Semin Thromb Hemost 2022
7
50

Clinical Significance of Vascular Occlusive Events following Moderate-to-Severe Traumatic Brain Injury: An Observational Cohort Study.
Alexander Fletcher-Sandersjöö, Charles Tatter, Jonathan Tjerkaski, Jiri Bartek, Mikael Svensson, Eric Peter Thelin, Bo-Michael Bellander. Semin Thromb Hemost 2022
1
100

Major and Minor Classifications for Surgery in People With Hemophilia: A Literature Review.
Luigi Piero Solimeno, Miguel A Escobar, Snejana Krassova, Stephanie Seremetis. Clin Appl Thromb Hemost 2018
17
50

The EAHAD blood coagulation factor VII variant database.
Muriel Giansily-Blaizot, Pavithra M Rallapalli, Stephen J Perkins, Geoffrey Kemball-Cook, Daniel J Hampshire, Keith Gomez, Christopher A Ludlam, John H McVey. Hum Mutat 2020
9
50

Is prophylaxis required for delivery in women with factor VII deficiency?
L M Baumann Kreuziger, Colleen T Morton, Mark T Reding. Haemophilia 2013
22
50

Phenotypic and genotypic characterization of four factor VII deficiency patients from central China.
Hui Liu, Hua-Fang Wang, Zhi-peng Cheng, Qing-yun Wang, Bei Hu, Wei Zeng, Ying-ying Wu, Tao Guo, Liang Tang, Yu Hu. Blood Coagul Fibrinolysis 2015
3
50

Inhibitor in Congenital Factor VII Deficiency; a Rare but Serious Therapeutic Challenge-A Systematic Literature Review.
Nahid Ramezanpour, Farhad Zaker, Arijit Biswas, Akbar Dorgalaleh. J Clin Med 2021
3
50

[Molecular genetic analysis for a pedigree with severe hereditary coagulation factor VII deficiency].
Qiu-lan Ding, Hong-li Wang, Xue-feng Wang, Ming-shan Wang, Qi-hua Fu, Wen-man Wu, Yi-qun Hu, Zhen-yi Wang. Zhonghua Nei Ke Za Zhi 2003
1
100

[Congenital factor Ⅶ deficiency: a retrospective analysis of 43 cases].
C Y Qu, D L Zhang, X F Liu, F Xue, W Liu, Y F Chen, R F Fu, L Zhang, R C Yang. Zhonghua Xue Ye Xue Za Zhi 2020
1
100



Gynecological and obstetrical manifestations of inherited bleeding disorders in women.
F Peyvandi, I Garagiola, M Menegatti. J Thromb Haemost 2011
40
50


UMD (Universal Mutation Database): 2005 update.
Christophe Béroud, Dalil Hamroun, Gwenaëlle Collod-Béroud, Catherine Boileau, Thierry Soussi, Mireille Claustres. Hum Mutat 2005
89
50

Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency.
M Borhany, H Boijout, J-L Pellequer, T Shamsi, G Moulis, P Aguilar-Martinez, J-F Schved, M Giansily-Blaizot. Haemophilia 2013
12
50

[Inherited coagulation factor VII deficiency caused by double heterozygotic mutations Arg304Gln and Arg304Trp].
Qiu-lan Ding, Hong-li Wang, Xue-feng Wang, Ming-shan Wang, Qi-hua Fu, Wen-man Wu, Yi-qun Hu, Zhen-yi Wang. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2003
3
50

Congenital FVII deficiency and thrombotic events after replacement therapy.
Antonio Girolami, Irene Bertozzi, Ignazio Rigoni, Rodolfo Muzzolon, Silvia Vettore. J Thromb Thrombolysis 2011
30
50

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency.
Guglielmo Mariani, Falko H Herrmann, Alberto Dolce, Angelika Batorova, Daniela Etro, Flora Peyvandi, Karin Wulff, Jean F Schved, Günter Auerswald, Jorgen Ingerslev,[...]. Thromb Haemost 2005
147
50

Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency.
Matteo Nicola Dario Di Minno, Alberto Dolce, Guglielmo Mariani. Thromb Haemost 2013
34
50

Thrombosis in inherited factor VII deficiency.
G Mariani, F H Herrmann, S Schulman, A Batorova, K Wulff, D Etro, A Dolce, G Auerswald, J Astermark, J-F Schved,[...]. J Thromb Haemost 2003
78
50

Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER).
Mariasanta Napolitano, Muriel Giansily-Blaizot, Alberto Dolce, Jean F Schved, Guenter Auerswald, Jørgen Ingerslev, Jens Bjerre, Carmen Altisent, Pimlak Charoenkwan, Lisa Michaels,[...]. Haematologica 2013
64
50

The Ensembl gene annotation system.
Bronwen L Aken, Sarah Ayling, Daniel Barrell, Laura Clarke, Valery Curwen, Susan Fairley, Julio Fernandez Banet, Konstantinos Billis, Carlos García Girón, Thibaut Hourlier,[...]. Database (Oxford) 2016
497
50

Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency.
M Lak, F Peyvandi, A Ali Sharifian, K Karimi, P M Mannucci. J Thromb Haemost 2003
68
50

Treatment of rare factor deficiencies other than hemophilia.
Marzia Menegatti, Flora Peyvandi. Blood 2019
49
50

F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study.
Gabriele Quintavalle, Federica Riccardi, Gianna Franca Rivolta, Davide Martorana, Caterina Di Perna, Antonio Percesepe, Annarita Tagliaferri. Thromb Haemost 2017
8
50

Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia.
M Lak, M Keihani, F Elahi, F Peyvandi, P M Mannucci. Br J Haematol 1999
185
50

Rare bleeding disorders: diagnosis and treatment.
Roberta Palla, Flora Peyvandi, Amy D Shapiro. Blood 2015
157
50

Prenatal and peripartum management of congenital afibrinogenaemia.
T Kobayashi, N Kanayama, N Tokunaga, T Asahina, T Terao. Br J Haematol 2000
72
50

Congenital afibrinogenemia and recurrent early abortion: a case report.
S Evron, S O Anteby, A Brzezinsky, A Samueloff, A Eldor. Eur J Obstet Gynecol Reprod Biol 1985
43
50

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders.
F Peyvandi, R Palla, M Menegatti, S M Siboni, S Halimeh, B Faeser, H Pergantou, H Platokouki, P Giangrande, K Peerlinck,[...]. J Thromb Haemost 2012
250
50

Nomenclature of genetic variants in hemostasis.
A C Goodeve, P H Reitsma, J H McVey. J Thromb Haemost 2011
33
50


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.