A citation-based method for searching scientific literature

Patrick Yap, Ravi Savarirayan. Am J Med Genet A 2016
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


Nosology and classification of genetic skeletal disorders: 2015 revision.
Luisa Bonafe, Valerie Cormier-Daire, Christine Hall, Ralph Lachman, Geert Mortier, Stefan Mundlos, Gen Nishimura, Luca Sangiorgi, Ravi Savarirayan, David Sillence,[...]. Am J Med Genet A 2015
312
37

Best practices in peri-operative management of patients with skeletal dysplasias.
Klane K White, Viviana Bompadre, Michael J Goldberg, Michael B Bober, Tae-Joon Cho, Julie E Hoover-Fong, Melita Irving, William G Mackenzie, Shawn E Kamps, Cathleen Raggio,[...]. Am J Med Genet A 2017
16
37

Best practices in the evaluation and treatment of foramen magnum stenosis in achondroplasia during infancy.
Klane K White, Viviana Bompadre, Michael J Goldberg, Michael B Bober, Jeffrey W Campbell, Tae-Joon Cho, Julie Hoover-Fong, William Mackenzie, Shawn E Parnell, Cathleen Raggio,[...]. Am J Med Genet A 2016
32
37

C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia.
Ravi Savarirayan, Melita Irving, Carlos A Bacino, Bret Bostwick, Joel Charrow, Valerie Cormier-Daire, Kim-Hanh Le Quan Sang, Patricia Dickson, Paul Harmatz, John Phillips,[...]. N Engl J Med 2019
51
37

Neutral endopeptidase-resistant C-type natriuretic peptide variant represents a new therapeutic approach for treatment of fibroblast growth factor receptor 3-related dwarfism.
Daniel J Wendt, Melita Dvorak-Ewell, Sherry Bullens, Florence Lorget, Sean M Bell, Jeff Peng, Sianna Castillo, Mika Aoyagi-Scharber, Charles A O'Neill, Pavel Krejci,[...]. J Pharmacol Exp Ther 2015
56
25

Enhancement of drug delivery to bone: characterization of human tissue-nonspecific alkaline phosphatase tagged with an acidic oligopeptide.
Tatsuo Nishioka, Shunji Tomatsu, Monica A Gutierrez, Ken-ichi Miyamoto, Georgeta G Trandafirescu, Patricia L C Lopez, Jeffrey H Grubb, Rie Kanai, Hironori Kobayashi, Seiji Yamaguchi,[...]. Mol Genet Metab 2006
57
25

Bisphosphonate therapy for osteogenesis imperfecta.
Kerry Dwan, Carrie A Phillipi, Robert D Steiner, Donald Basel. Cochrane Database Syst Rev 2016
81
25

Raloxifene reduces skeletal fractures in an animal model of osteogenesis imperfecta.
Alycia G Berman, Joseph M Wallace, Zachary R Bart, Matthew R Allen. Matrix Biol 2016
17
25

Meclozine promotes longitudinal skeletal growth in transgenic mice with achondroplasia carrying a gain-of-function mutation in the FGFR3 gene.
Masaki Matsushita, Satoru Hasegawa, Hiroshi Kitoh, Kensaku Mori, Bisei Ohkawara, Akihiro Yasoda, Akio Masuda, Naoki Ishiguro, Kinji Ohno. Endocrinology 2015
29
25

A height-for-age growth reference for children with achondroplasia: Expanded applications and comparison with original reference data.
Julie Hoover-Fong, John McGready, Kerry Schulze, Adekemi Yewande Alade, Charles I Scott. Am J Med Genet A 2017
21
25

Body mass index (BMI): the case for condition-specific cut-offs for overweight and obesity in skeletal dysplasias.
Kerry J Schulze, Yewande Adekemi Alade, John McGready, Julie E Hoover-Fong. Am J Med Genet A 2013
8
25

Research priorities for multi-institutional collaborative research in surgical education.
Dimitrios Stefanidis, Amalia Cochran, Nick Sevdalis, John Mellinger, Roy Phitayakorn, Maura Sullivan, Linda Barney. Am J Surg 2015
22
25

Spinal involvement in mucopolysaccharidosis IVA (Morquio-Brailsford or Morquio A syndrome): presentation, diagnosis and management.
Guirish A Solanki, Kenneth W Martin, Mary C Theroux, Christina Lampe, Klane K White, Renée Shediac, Christian G Lampe, Michael Beck, William G Mackenzie, Christian J Hendriksz,[...]. J Inherit Metab Dis 2013
61
25

A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype.
Paulien A Terhal, Rutger Jan A J Nievelstein, Eva J J Verver, Vedat Topsakal, Paula van Dommelen, Kristien Hoornaert, Martine Le Merrer, Andreas Zankl, Marleen E H Simon, Sarah F Smithson,[...]. Am J Med Genet A 2015
41
25



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
25

Development of health equity indicators in primary health care organizations using a modified Delphi.
Sabrina T Wong, Annette J Browne, Colleen Varcoe, Josée Lavoie, Alycia Fridkin, Victoria Smye, Olive Godwin, David Tu. PLoS One 2014
15
25

Best practice guidelines regarding prenatal evaluation and delivery of patients with skeletal dysplasia.
Ravi Savarirayan, Judith P Rossiter, Julie E Hoover-Fong, Melita Irving, Viviana Bompadre, Michael J Goldberg, Michael B Bober, Tae-Joon Cho, Shawn E Kamps, William G Mackenzie,[...]. Am J Obstet Gynecol 2018
13
25

Spinal Cord Injury After Extremity Surgery in Children With Thoracic Kyphosis.
Blazej Pruszczynski, William G Mackenzie, Kenneth Rogers, Klane K White. Clin Orthop Relat Res 2015
11
25

Achondroplasia.
William A Horton, Judith G Hall, Jacqueline T Hecht. Lancet 2007
268
25

Current Care and Investigational Therapies in Achondroplasia.
Sheila Unger, Luisa Bonafé, Elvire Gouze. Curr Osteoporos Rep 2017
24
25

Optimal management of complications associated with achondroplasia.
Penny J Ireland, Verity Pacey, Andreas Zankl, Priya Edwards, Leanne M Johnston, Ravi Savarirayan. Appl Clin Genet 2014
27
25

Factors associated with health-related quality of life (HRQOL) in adults with short stature skeletal dysplasias.
Nitasha Dhiman, Alia Albaghdadi, Cheryl K Zogg, Meesha Sharma, Julie E Hoover-Fong, Michael C Ain, Adil H Haider. Qual Life Res 2017
18
25

Cross-sectional assessment of pain and physical function in skeletal dysplasia patients.
Y Alade, D Tunkel, K Schulze, J McGready, G Jallo, M Ain, T Yost, J Hoover-Fong. Clin Genet 2013
19
25

Medical complications of achondroplasia: a multicentre patient review.
A G Hunter, A Bankier, J G Rogers, D Sillence, C I Scott. J Med Genet 1998
132
25

Achondroplasia: a comprehensive clinical review.
Richard M Pauli. Orphanet J Rare Dis 2019
73
25

Mortality in achondroplasia study: a 42-year follow-up.
Julia Wynn, Terri M King, Michael J Gambello, D Kim Waller, Jacqueline T Hecht. Am J Med Genet A 2007
67
25


Health supervision for children with achondroplasia.
Tracy L Trotter, Judith G Hall. Pediatrics 2005
110
25

Current knowledge of medical complications in adults with achondroplasia: A scoping review.
Svein O Fredwall, Grethe Maanum, Heidi Johansen, Hildegun Snekkevik, Ravi Savarirayan, Ingeborg B Lidal. Clin Genet 2020
14
25

Functional health status of adults with achondroplasia.
N N Mahomed, M Spellmann, M J Goldberg. Am J Med Genet 1998
32
25

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
152
25

Denosumab for prevention of fractures in postmenopausal women with osteoporosis.
Steven R Cummings, Javier San Martin, Michael R McClung, Ethel S Siris, Richard Eastell, Ian R Reid, Pierre Delmas, Holly B Zoog, Matt Austin, Andrea Wang,[...]. N Engl J Med 2009
12

Advances in treatment of achondroplasia and osteoarthritis.
Kendra A Klag, William A Horton. Hum Mol Genet 2016
27
12

Hypophosphatasia - pathophysiology and treatment.
José Luis Millán, Horacio Plotkin. Actual osteol 2012
19
12

Overview of the mucopolysaccharidoses.
Joseph Muenzer. Rheumatology (Oxford) 2011
240
12

Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled study.
L M Ward, F Rauch, M P Whyte, J D'Astous, P E Gates, D Grogan, E L Lester, R E McCall, T A Pressly, J O Sanders,[...]. J Clin Endocrinol Metab 2011
122
12

Update on the evaluation and treatment of osteogenesis imperfecta.
Jennifer Harrington, Etienne Sochett, Andrew Howard. Pediatr Clin North Am 2014
37
12

Statin treatment rescues FGFR3 skeletal dysplasia phenotypes.
Akihiro Yamashita, Miho Morioka, Hiromi Kishi, Takeshi Kimura, Yasuhito Yahara, Minoru Okada, Kaori Fujita, Hideaki Sawai, Shiro Ikegawa, Noriyuki Tsumaki. Nature 2014
124
12

Personalized Pharmacoperones for Lysosomal Storage Disorder: Approach for Next-Generation Treatment.
S A Syed Haneef, C George Priya Doss. Adv Protein Chem Struct Biol 2016
12
12

Skeletal changes in rats given daily subcutaneous injections of recombinant human parathyroid hormone (1-34) for 2 years and relevance to human safety.
John L Vahle, Masahiko Sato, Gerald G Long, Jamie K Young, Paul C Francis, Jeffery A Engelhardt, Michael S Westmore, Yanfei Linda, James B Nold. Toxicol Pathol 2002
421
12

Skeletal dysplasias.
Deborah Krakow. Clin Perinatol 2015
45
12

Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase (laronidase).
James E Wraith, Lorne A Clarke, Michael Beck, Edwin H Kolodny, Gregory M Pastores, Joseph Muenzer, David M Rapoport, Kenneth I Berger, Stuart J Swiedler, Emil D Kakkis,[...]. J Pediatr 2004
409
12


CNS-directed gene therapy for the treatment of neurologic and somatic mucopolysaccharidosis type II (Hunter syndrome).
Sandra Motas, Virginia Haurigot, Miguel Garcia, Sara Marcó, Albert Ribera, Carles Roca, Xavier Sánchez, Víctor Sánchez, Maria Molas, Joan Bertolin,[...]. JCI Insight 2016
32
12

Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients.
Yi Liu, Jiawei Wang, Doudou Ma, Fang Lv, Xiaojie Xu, Weibo Xia, Yan Jiang, Ou Wang, Xiaoping Xing, Peiran Zhou,[...]. Clin Chim Acta 2016
7
14

Recent developments in osteogenesis imperfecta.
Joseph L Shaker, Carolyne Albert, Jessica Fritz, Gerald Harris. F1000Res 2015
25
12

Systemic administration of C-type natriuretic peptide as a novel therapeutic strategy for skeletal dysplasias.
Akihiro Yasoda, Hidetomo Kitamura, Toshihito Fujii, Eri Kondo, Naoaki Murao, Masako Miura, Naotetsu Kanamoto, Yasato Komatsu, Hiroshi Arai, Kazuwa Nakao. Endocrinology 2009
78
12

New perspectives on osteogenesis imperfecta.
Antonella Forlino, Wayne A Cabral, Aileen M Barnes, Joan C Marini. Nat Rev Endocrinol 2011
355
12


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.