A citation-based method for searching scientific literature

Gretchen MacCarrick, James H Black, Sarah Bowdin, Ismail El-Hamamsy, Pamela A Frischmeyer-Guerrerio, Anthony L Guerrerio, Paul D Sponseller, Bart Loeys, Harry C Dietz. Genet Med 2014
Times Cited: 267







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



Times Cited
  Times     Co-cited
Similarity


A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
Bart L Loeys, Junji Chen, Enid R Neptune, Daniel P Judge, Megan Podowski, Tammy Holm, Jennifer Meyers, Carmen C Leitch, Nicholas Katsanis, Neda Sharifi,[...]. Nat Genet 2005
49

Aneurysm syndromes caused by mutations in the TGF-beta receptor.
Bart L Loeys, Ulrike Schwarze, Tammy Holm, Bert L Callewaert, George H Thomas, Hariyadarshi Pannu, Julie F De Backer, Gretchen L Oswald, Sofie Symoens, Sylvie Manouvrier,[...]. N Engl J Med 2006
48

Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome.
Josephina A N Meester, Aline Verstraeten, Dorien Schepers, Maaike Alaerts, Lut Van Laer, Bart L Loeys. Ann Cardiothorac Surg 2017
122
19

The revised Ghent nosology for the Marfan syndrome.
Bart L Loeys, Harry C Dietz, Alan C Braverman, Bert L Callewaert, Julie De Backer, Richard B Devereux, Yvonne Hilhorst-Hofstee, Guillaume Jondeau, Laurence Faivre, Dianna M Milewicz,[...]. J Med Genet 2010
18

Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis.
Ingrid M B H van de Laar, Rogier A Oldenburg, Gerard Pals, Jolien W Roos-Hesselink, Bianca M de Graaf, Judith M A Verhagen, Yvonne M Hoedemaekers, Rob Willemsen, Lies-Anne Severijnen, Hanka Venselaar,[...]. Nat Genet 2011
432
18

2014 ESC Guidelines on the diagnosis and treatment of aortic diseases: Document covering acute and chronic aortic diseases of the thoracic and abdominal aorta of the adult. The Task Force for the Diagnosis and Treatment of Aortic Diseases of the European Society of Cardiology (ESC).
Raimund Erbel, Victor Aboyans, Catherine Boileau, Eduardo Bossone, Roberto Di Bartolomeo, Holger Eggebrecht, Arturo Evangelista, Volkmar Falk, Herbert Frank, Oliver Gaemperli,[...]. Eur Heart J 2014
17

International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium).
Guillaume Jondeau, Jacques Ropers, Ellen Regalado, Alan Braverman, Arturo Evangelista, Guisela Teixedo, Julie De Backer, Laura Muiño-Mosquera, Sophie Naudion, Cecile Zordan,[...]. Circ Cardiovasc Genet 2016
101
17

TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.
Catherine Boileau, Dong-Chuan Guo, Nadine Hanna, Ellen S Regalado, Delphine Detaint, Limin Gong, Mathilde Varret, Siddharth K Prakash, Alexander H Li, Hyacintha d'Indy,[...]. Nat Genet 2012
236
16

Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.
Mark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, Jefferson J Doyle, Elena Gallo, Justyna Fert-Bober, Marlies J E Kempers, Elliot K Fishman, Yichun Chen, Loretha Myers,[...]. Nat Genet 2012
285
14

Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome.
Ingrid M B H van de Laar, Denise van der Linde, Edwin H G Oei, Pieter K Bos, Johannes H Bessems, Sita M Bierma-Zeinstra, Belle L van Meer, Gerard Pals, Rogier A Oldenburg, Jos A Bekkers,[...]. J Med Genet 2012
158
14

Increased vertebral artery tortuosity index is associated with adverse outcomes in children and young adults with connective tissue disorders.
Shaine A Morris, Darren B Orbach, Tal Geva, Michael N Singh, Kimberlee Gauvreau, Ronald V Lacro. Circulation 2011
132
13

Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissections.
Aida M Bertoli-Avella, Elisabeth Gillis, Hiroko Morisaki, Judith M A Verhagen, Bianca M de Graaf, Gerarda van de Beek, Elena Gallo, Boudewijn P T Kruithof, Hanka Venselaar, Loretha A Myers,[...]. J Am Coll Cardiol 2015
164
13

A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3.
Dorien Schepers, Giada Tortora, Hiroko Morisaki, Gretchen MacCarrick, Mark Lindsay, David Liang, Sarju G Mehta, Jennifer Hague, Judith Verhagen, Ingrid van de Laar,[...]. Hum Mutat 2018
78
15


Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type.
M Pepin, U Schwarze, A Superti-Furga, P H Byers. N Engl J Med 2000
769
12

Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome.
Peter H Byers, John Belmont, James Black, Julie De Backer, Michael Frank, Xavier Jeunemaitre, Diana Johnson, Melanie Pepin, Leema Robert, Lynn Sanders,[...]. Am J Med Genet C Semin Med Genet 2017
127
12

The 2017 international classification of the Ehlers-Danlos syndromes.
Fransiska Malfait, Clair Francomano, Peter Byers, John Belmont, Britta Berglund, James Black, Lara Bloom, Jessica M Bowen, Angela F Brady, Nigel P Burrows,[...]. Am J Med Genet C Semin Med Genet 2017
662
11

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
11

Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection.
Marjolijn Renard, Catherine Francis, Rajarshi Ghosh, Alan F Scott, P Dane Witmer, Lesley C Adès, Gregor U Andelfinger, Pauline Arnaud, Catherine Boileau, Bert L Callewaert,[...]. J Am Coll Cardiol 2018
95
11

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.
H C Dietz, G R Cutting, R E Pyeritz, C L Maslen, L Y Sakai, G M Corson, E G Puffenberger, A Hamosh, E J Nanthakumar, S M Curristin. Nature 1991
11

Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.
Dong-Chuan Guo, Hariyadarshi Pannu, Van Tran-Fadulu, Christina L Papke, Robert K Yu, Nili Avidan, Scott Bourgeois, Anthony L Estrera, Hazim J Safi, Elizabeth Sparks,[...]. Nat Genet 2007
550
11

Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome.
Jennifer P Habashi, Daniel P Judge, Tammy M Holm, Ronald D Cohn, Bart L Loeys, Timothy K Cooper, Loretha Myers, Erin C Klein, Guosheng Liu, Carla Calvi,[...]. Science 2006
11

Early surgical experience with Loeys-Dietz: a new syndrome of aggressive thoracic aortic aneurysm disease.
Jason A Williams, Bart L Loeys, Lois U Nwakanma, Harry C Dietz, Philip J Spevak, Nishant D Patel, Katrien François, Julie DeBacker, Vincent L Gott, Luca A Vricella,[...]. Ann Thorac Surg 2007
167
11

Lineage-specific events underlie aortic root aneurysm pathogenesis in Loeys-Dietz syndrome.
Elena Gallo MacFarlane, Sarah J Parker, Joseph Y Shin, Benjamin E Kang, Shira G Ziegler, Tyler J Creamer, Rustam Bagirzadeh, Djahida Bedja, Yichun Chen, Juan F Calderon,[...]. J Clin Invest 2019
52
19

Cardiovascular Manifestations and Complications of Loeys-Dietz Syndrome: CT and MR Imaging Findings.
William W Loughborough, Kishore S Minhas, Jonathan C L Rodrigues, Stephen M Lyen, Helen E Burt, Nathan E Manghat, Marcus J Brooks, Graham Stuart, Mark C K Hamilton. Radiographics 2018
20
50

Loeys-Dietz syndrome.
Lut Van Laer, Harry Dietz, Bart Loeys. Adv Exp Med Biol 2014
67
14

Neuroradiologic manifestations of Loeys-Dietz syndrome type 1.
V J Rodrigues, S Elsayed, B L Loeys, H C Dietz, D M Yousem. AJNR Am J Neuroradiol 2009
71
12

The Loeys-Dietz syndrome: an update for the clinician.
Christine Van Hemelrijk, Marjolijn Renard, Bart Loeys. Curr Opin Cardiol 2010
94
9

Genetics of Thoracic and Abdominal Aortic Diseases.
Amélie Pinard, Gregory T Jones, Dianna M Milewicz. Circ Res 2019
128
9


Familial thoracic aortic aneurysms and dissections--incidence, modes of inheritance, and phenotypic patterns.
Gonzalo Albornoz, Michael A Coady, Michele Roberts, Ryan R Davies, Maryann Tranquilli, John A Rizzo, John A Elefteriades. Ann Thorac Surg 2006
271
9

Atenolol versus losartan in children and young adults with Marfan's syndrome.
Ronald V Lacro, Harry C Dietz, Lynn A Sleeper, Anji T Yetman, Timothy J Bradley, Steven D Colan, Gail D Pearson, E Seda Selamet Tierney, Jami C Levine, Andrew M Atz,[...]. N Engl J Med 2014
296
9

Angiotensin II-dependent TGF-β signaling contributes to Loeys-Dietz syndrome vascular pathogenesis.
Elena M Gallo, David C Loch, Jennifer P Habashi, Juan F Calderon, Yichun Chen, Djahida Bedja, Christel van Erp, Elizabeth E Gerber, Sarah J Parker, Kimberly Sauls,[...]. J Clin Invest 2014
155
9

SMAD3 pathogenic variants: risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium.
Ellen M Hostetler, Ellen S Regalado, Dong-Chuan Guo, Nadine Hanna, Pauline Arnaud, Laura Muiño-Mosquera, Bert Louis Callewaert, Kwanghyuk Lee, Suzanne M Leal, Stephanie E Wallace,[...]. J Med Genet 2019
26
34

Heritable Thoracic Aortic Disease Genes in Sporadic Aortic Dissection.
Dong-Chuan Guo, Ellen M Hostetler, Yuxin Fan, Richard J Kulmacz, Di Zhang, Deborah A Nickerson, Suzanne M Leal, Scott A LeMaire, Ellen S Regalado, Dianna M Milewicz. J Am Coll Cardiol 2017
28
28


SMAD2 Mutations Are Associated with Arterial Aneurysms and Dissections.
Dimitra Micha, Dong-Chuan Guo, Yvonne Hilhorst-Hofstee, Fop van Kooten, Dian Atmaja, Eline Overwater, Ferdy K Cayami, Ellen S Regalado, René van Uffelen, Hanka Venselaar,[...]. Hum Mutat 2015
52
15

Cardiovascular operations for Loeys-Dietz syndrome: Intermediate-term results.
Nishant D Patel, Todd Crawford, J Trent Magruder, Diane E Alejo, Narutoshi Hibino, James Black, Harry C Dietz, Luca A Vricella, Duke E Cameron. J Thorac Cardiovasc Surg 2017
29
27

Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.
Dong-chuan Guo, Ellen Regalado, Darren E Casteel, Regie L Santos-Cortez, Limin Gong, Jeong Joo Kim, Sarah Dyack, S Gabrielle Horne, Guijuan Chang, Guillaume Jondeau,[...]. Am J Hum Genet 2013
143
7

Survival is affected by mutation type and molecular mechanism in vascular Ehlers-Danlos syndrome (EDS type IV).
Melanie G Pepin, Ulrike Schwarze, Kenneth M Rice, Mingdong Liu, Dru Leistritz, Peter H Byers. Genet Med 2014
123
7


TGF-β Signaling-Related Genes and Thoracic Aortic Aneurysms and Dissections.
Norifumi Takeda, Hironori Hara, Takayuki Fujiwara, Tsubasa Kanaya, Sonoko Maemura, Issei Komuro. Int J Mol Sci 2018
63
11

Heterogeneity of aortic disease severity in patients with Loeys-Dietz syndrome.
Gisela Teixidó-Tura, Romy Franken, Valentina Galuppo, Laura Gutiérrez García-Moreno, Mar Borregan, Barbara J M Mulder, David García-Dorado, Artur Evangelista. Heart 2016
21
33

Aortic Disease Presentation and Outcome Associated With ACTA2 Mutations.
Ellen S Regalado, Dong-chuan Guo, Siddharth Prakash, Tracy A Bensend, Kelly Flynn, Anthony Estrera, Hazim Safi, David Liang, James Hyland, Anne Child,[...]. Circ Cardiovasc Genet 2015
74
9

The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers-Danlos syndrome.
Michael Frank, Juliette Albuisson, Brigitte Ranque, Lisa Golmard, Jean-Michael Mazzella, Laurence Bal-Theoleyre, Anne-Laure Fauret, Tristan Mirault, Nicolas Denarié, Elie Mousseaux,[...]. Eur J Hum Genet 2015
99
7

Musculoskeletal findings of Loeys-Dietz syndrome.
Gurkan Erkula, Paul D Sponseller, Laura C Paulsen, Gretchen L Oswald, Bart L Loeys, Harry C Dietz. J Bone Joint Surg Am 2010
49
14

Histopathologic findings in ascending aortas from individuals with Loeys-Dietz syndrome (LDS).
Joseph J Maleszewski, Dylan V Miller, Jie Lu, Harry C Dietz, Marc K Halushka. Am J Surg Pathol 2009
80
7


Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.
Ellen S Regalado, Dong-Chuan Guo, Carlos Villamizar, Nili Avidan, Dawna Gilchrist, Barbara McGillivray, Lorne Clarke, Francois Bernier, Regie L Santos-Cortez, Suzanne M Leal,[...]. Circ Res 2011
194
6

Familial thoracic aortic dilatations and dissections: a case control study.
A Biddinger, M Rocklin, J Coselli, D M Milewicz. J Vasc Surg 1997
147
6


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.