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: 273







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



Times Cited
  Times     Co-cited
Similarity


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
49

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

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
104
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

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
127
18

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
239
16

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
15

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
435
15

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
160
14

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
694
13

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
102
12

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
287
12

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
167
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
134
12

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
134
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
556
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
169
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

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
781
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
53
18

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
73
13

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

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
10

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
12

Genetics of Thoracic and Abdominal Aortic Diseases.
Amélie Pinard, Gregory T Jones, Dianna M Milewicz. Circ Res 2019
140
10

Loeys-Dietz syndrome.
Lut Van Laer, Harry Dietz, Bart Loeys. Adv Exp Med Biol 2014
68
14

The Loeys-Dietz syndrome: an update for the clinician.
Christine Van Hemelrijk, Marjolijn Renard, Bart Loeys. Curr Opin Cardiol 2010
94
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
156
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
27
33

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
31
25


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
301
8

TGFβ receptor mutations impose a strong predisposition for human allergic disease.
Pamela A Frischmeyer-Guerrerio, Anthony L Guerrerio, Gretchen Oswald, Kristin Chichester, Loretha Myers, Marc K Halushka, Maria Oliva-Hemker, Robert A Wood, Harry C Dietz. Sci Transl Med 2013
123
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

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
29
24

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
127
7

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
13

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
272
7

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
81
7

Loeys-Dietz syndrome: Intermediate-term outcomes of medically and surgically managed patients.
Muhammad Aftab, Frank S Cikach, Yuanjia Zhu, Jay J Idrees, Christina M Rigelsky, Vidyasagar Kalahasti, Eric E Roselli, Lars G Svensson. J Thorac Cardiovasc Surg 2019
19
31

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
144
6

Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations.
V Tran-Fadulu, H Pannu, D H Kim, G W Vick, C M Lonsford, A L Lafont, C Boccalandro, S Smart, K L Peterson, J Zenger Hain,[...]. J Med Genet 2009
120
6

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
23
26

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
76
7

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
107
6

Comparison of clinical presentations and outcomes between patients with TGFBR2 and FBN1 mutations in Marfan syndrome and related disorders.
David Attias, Chantal Stheneur, Carine Roy, Gwenaëlle Collod-Béroud, Delphine Detaint, Laurence Faivre, Marie-Ange Delrue, Laurence Cohen, Christine Francannet, Christophe Béroud,[...]. Circulation 2009
133
6


Marfan's syndrome.
Daniel P Judge, Harry C Dietz. Lancet 2005
727
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.