A citation-based method for searching scientific literature

Ronit Marom, Brien M Rabenhorst, Roy Morello. Eur J Endocrinol 2020
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Osteogenesis imperfecta.
Antonella Forlino, Joan C Marini. Lancet 2016
385
42

Nosology and classification of genetic skeletal disorders: 2019 revision.
Geert R Mortier, Daniel H Cohn, Valerie Cormier-Daire, Christine Hall, Deborah Krakow, Stefan Mundlos, Gen Nishimura, Stephen Robertson, Luca Sangiorgi, Ravi Savarirayan,[...]. Am J Med Genet A 2019
172
35

Osteogenesis imperfecta.
Joan C Marini, Antonella Forlino, Hans Peter Bächinger, Nick J Bishop, Peter H Byers, Anne De Paepe, Francois Fassier, Nadja Fratzl-Zelman, Kenneth M Kozloff, Deborah Krakow,[...]. Nat Rev Dis Primers 2017
237
35

Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta.
Ingo Grafe, Tao Yang, Stefanie Alexander, Erica P Homan, Caressa Lietman, Ming Ming Jiang, Terry Bertin, Elda Munivez, Yuqing Chen, Brian Dawson,[...]. Nat Med 2014
153
28

Osteogenesis imperfecta and therapeutics.
Roy Morello. Matrix Biol 2018
41
28

New perspectives on osteogenesis imperfecta.
Antonella Forlino, Wayne A Cabral, Aileen M Barnes, Joan C Marini. Nat Rev Endocrinol 2011
363
28

Genetic heterogeneity in osteogenesis imperfecta.
D O Sillence, A Senn, D M Danks. J Med Genet 1979
28

4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion.
Roberta Besio, Giusy Iula, Nadia Garibaldi, Lina Cipolla, Simone Sabbioneda, Marco Biggiogera, Joan C Marini, Antonio Rossi, Antonella Forlino. Biochim Biophys Acta Mol Basis Dis 2018
34
21

Skeletal Response to Soluble Activin Receptor Type IIB in Mouse Models of Osteogenesis Imperfecta.
Youngjae Jeong, Salah A Daghlas, Yixia Xie, Molly A Hulbert, Ferris M Pfeiffer, Mark R Dallas, Catherine L Omosule, R Scott Pearsall, Sarah L Dallas, Charlotte L Phillips. J Bone Miner Res 2018
17
21

Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.-14C>T mutation in all patients.
Frank Rauch, Pierre Moffatt, Moira Cheung, Peter Roughley, Liljana Lalic, Allan M Lund, Norman Ramirez, Somayyeh Fahiminiya, Jacek Majewski, Francis H Glorieux. J Med Genet 2013
70
21


Osteogenesis Imperfecta: New Perspectives From Clinical and Translational Research.
Josephine T Tauer, Marie-Eve Robinson, Frank Rauch. JBMR Plus 2019
34
21

Osteogenesis imperfecta-pathophysiology and therapeutic options.
Julia Etich, Lennart Leßmeier, Mirko Rehberg, Helge Sill, Frank Zaucke, Christian Netzer, Oliver Semler. Mol Cell Pediatr 2020
7
42

Signaling pathways affected by mutations causing osteogenesis imperfecta.
Julia Etich, Mirko Rehberg, Beate Eckes, Gerhard Sengle, Oliver Semler, Frank Zaucke. Cell Signal 2020
10
20

Metabolic phenotype in the mouse model of osteogenesis imperfecta.
Iris Boraschi-Diaz, Josephine T Tauer, Omar El-Rifai, Delphine Guillemette, Geneviève Lefebvre, Frank Rauch, Mathieu Ferron, Svetlana V Komarova. J Endocrinol 2017
12
16

Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.
Joan C Marini, Antonella Forlino, Wayne A Cabral, Aileen M Barnes, James D San Antonio, Sarah Milgrom, James C Hyland, Jarmo Körkkö, Darwin J Prockop, Anne De Paepe,[...]. Hum Mutat 2007
428
14

Cardiovascular disease in patients with osteogenesis imperfecta - a nationwide, register-based cohort study.
Lars Folkestad, Jannie Dahl Hald, Jeppe Gram, Bente L Langdahl, Anne Pernille Hermann, Axel Cp Diederichsen, Bo Abrahamsen, Kim Brixen. Int J Cardiol 2016
14
14

Effect of Anti-TGF-β Treatment in a Mouse Model of Severe Osteogenesis Imperfecta.
Josephine T Tauer, Sami Abdullah, Frank Rauch. J Bone Miner Res 2019
23
14

Mortality and Causes of Death in Patients With Osteogenesis Imperfecta: A Register-Based Nationwide Cohort Study.
Lars Folkestad, Jannie Dahl Hald, Vladimir Canudas-Romo, Jeppe Gram, Anne Pernille Hermann, Bente Langdahl, Bo Abrahamsen, Kim Brixen. J Bone Miner Res 2016
43
14

Bisphosphonates for the prevention of fractures in osteogenesis imperfecta: meta-analysis of placebo-controlled trials.
Jannie D Hald, Evangelos Evangelou, Bente L Langdahl, Stuart H Ralston. J Bone Miner Res 2015
58
14

Fracture Rates and Fracture Sites in Patients With Osteogenesis Imperfecta: A Nationwide Register-Based Cohort Study.
Lars Folkestad, Jannie Dahl Hald, Annette Kjaer Ersbøll, Jeppe Gram, Anne Pernille Hermann, Bente Langdahl, Bo Abrahamsen, Kim Brixen. J Bone Miner Res 2017
47
14

Bisphosphonate therapy for osteogenesis imperfecta.
Kerry Dwan, Carrie A Phillipi, Robert D Steiner, Donald Basel. Cochrane Database Syst Rev 2016
85
14

Cyclic administration of pamidronate in children with severe osteogenesis imperfecta.
F H Glorieux, N J Bishop, H Plotkin, G Chabot, G Lanoue, R Travers. N Engl J Med 1998
614
14

Burosumab Therapy in Children with X-Linked Hypophosphatemia.
Thomas O Carpenter, Michael P Whyte, Erik A Imel, Annemieke M Boot, Wolfgang Högler, Agnès Linglart, Raja Padidela, William Van't Hoff, Meng Mao, Chao-Yin Chen,[...]. N Engl J Med 2018
163
14

Tissue-nonspecific alkaline phosphatase is an anti-inflammatory nucleotidase.
L Bessueille, A Briolay, J Como, S Mebarek, C Mansouri, M Gleizes, A El Jamal, R Buchet, C Dumontet, E L Matera,[...]. Bone 2020
15
14


Parallel mechanisms suppress cochlear bone remodeling to protect hearing.
Emmanuel J Jáuregui, Omar Akil, Claire Acevedo, Faith Hall-Glenn, Betty S Tsai, Hrishikesh A Bale, Ellen Liebenberg, Mary Beth Humphrey, Robert O Ritchie, Lawrence R Lustig,[...]. Bone 2016
21
14

Pharmacological and biological therapeutic strategies for osteogenesis imperfecta.
Ronit Marom, Yi-Chien Lee, Ingo Grafe, Brendan Lee. Am J Med Genet C Semin Med Genet 2016
32
14

Teriparatide treatment in adult patients with osteogenesis imperfecta type I.
Davide Gatti, Maurizio Rossini, Ombretta Viapiana, Maria Rosaria Povino, Saverio Liuzza, Elena Fracassi, Luca Idolazzi, Silvano Adami. Calcif Tissue Int 2013
45
14

BPS804 Anti-Sclerostin Antibody in Adults With Moderate Osteogenesis Imperfecta: Results of a Randomized Phase 2a Trial.
Francis H Glorieux, Jean-Pierre Devogelaer, Michaela Durigova, Stefan Goemaere, Sarah Hemsley, Franz Jakob, Uwe Junker, Jon Ruckle, Lothar Seefried, Peter J Winkle. J Bone Miner Res 2017
51
14

Skeletal dysplasias.
Deborah Krakow. Clin Perinatol 2015
48
14

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.
Aileen M Barnes, Weizhong Chang, Roy Morello, Wayne A Cabral, MaryAnn Weis, David R Eyre, Sergey Leikin, Elena Makareeva, Natalia Kuznetsova, Thomas E Uveges,[...]. N Engl J Med 2006
197
14

Evaluation of teriparatide treatment in adults with osteogenesis imperfecta.
Eric S Orwoll, Jay Shapiro, Sandra Veith, Ying Wang, Jodi Lapidus, Chaim Vanek, Jan L Reeder, Tony M Keaveny, David C Lee, Mary A Mullins,[...]. J Clin Invest 2014
86
14

Pre- and postnatal transplantation of fetal mesenchymal stem cells in osteogenesis imperfecta: a two-center experience.
Cecilia Götherström, Magnus Westgren, S W Steven Shaw, Eva Aström, Arijit Biswas, Peter H Byers, Citra N Z Mattar, Gail E Graham, Jahan Taslimi, Uwe Ewald,[...]. Stem Cells Transl Med 2014
99
14

Attenuated BMP1 function compromises osteogenesis, leading to bone fragility in humans and zebrafish.
P V Asharani, Katharina Keupp, Oliver Semler, Wenshen Wang, Yun Li, Holger Thiele, Gökhan Yigit, Esther Pohl, Jutta Becker, Peter Frommolt,[...]. Am J Hum Genet 2012
132
14

Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
Rebecca C Pollitt, Vrinda Saraff, Ann Dalton, Emma A Webb, Nick J Shaw, Glenda J Sobey, M Zulf Mughal, Emma Hobson, Farhan Ali, Nicholas J Bishop,[...]. Am J Med Genet A 2016
18
14

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
14

Romosozumab Treatment in Postmenopausal Women with Osteoporosis.
Felicia Cosman, Daria B Crittenden, Jonathan D Adachi, Neil Binkley, Edward Czerwinski, Serge Ferrari, Lorenz C Hofbauer, Edith Lau, E Michael Lewiecki, Akimitsu Miyauchi,[...]. N Engl J Med 2016
565
14

Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate.
Roberta Besio, Nadia Garibaldi, Laura Leoni, Lina Cipolla, Simone Sabbioneda, Marco Biggiogera, Monica Mottes, Mona Aglan, Ghada A Otaify, Samia A Temtamy,[...]. Dis Model Mech 2019
16
14

The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta.
Roberta Gioia, Francesca Tonelli, Ilaria Ceppi, Marco Biggiogera, Sergey Leikin, Shannon Fisher, Elena Tenedini, Timur A Yorgan, Thorsten Schinke, Kun Tian,[...]. Hum Mol Genet 2017
39
14

Whole genome sequencing of consanguineous families reveals novel pathogenic variants in intellectual disability.
Ann-Charlotte Thuresson, Cecilia Soussi Zander, Jin J Zhao, Jonatan Halvardson, Khurram Maqbool, Else Månsson, Eric Stenninger, Ulrika Holmlund, Ylva Öhrner, Lars Feuk. Clin Genet 2019
7
14

First reported case of Steel syndrome in the European population: A novel homozygous mutation in COL27A1 and review of the literature.
Evie Kritioti, Athina Theodosiou, Nayia Nicolaou, Angelos Alexandrou, Ioannis Papaevripidou, Elisavet Efstathiou, Violetta Christophidou-Anastasiadou, Carolina Sismani, George A Tanteles. Eur J Med Genet 2020
3
33

Autozygome and high throughput confirmation of disease genes candidacy.
Sateesh Maddirevula, Fatema Alzahrani, Mohammed Al-Owain, Mohammad A Al Muhaizea, Husam R Kayyali, Amal AlHashem, Zuhair Rahbeeni, Maha Al-Otaibi, Hamad I Alzaidan, Ameera Balobaid,[...]. Genet Med 2019
45
7




Collagens--structure, function, and biosynthesis.
K Gelse, E Pöschl, T Aigner. Adv Drug Deliv Rev 2003
997
7

Mutations in COL27A1 cause Steel syndrome and suggest a founder mutation effect in the Puerto Rican population.
Claudia Gonzaga-Jauregui, Candace N Gamble, Bo Yuan, Samantha Penney, Shalini Jhangiani, Donna M Muzny, Richard A Gibbs, James R Lupski, Jacqueline T Hecht. Eur J Hum Genet 2015
31
7

Three new patients with Steel syndrome and a Puerto Rican specific COL27A1 mutation.
Louise Amlie-Wolf, Sue Moyer-Harasink, Ann-Marie Carr, Philip Giampietro, Adele Schneider, Mitchell Simon. Am J Med Genet A 2020
4
25



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.