A citation-based method for searching scientific literature

Nobutaka Hanagata, Xianglan Li, Hiromi Morita, Taro Takemura, Jie Li, Takashi Minowa. J Bone Miner Metab 2011
Times Cited: 74







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



Times Cited
  Times     Co-cited
Similarity


Bril: a novel bone-specific modulator of mineralization.
Pierre Moffatt, Marie-Helene Gaumond, Patrick Salois, Karine Sellin, Marie-Claude Bessette, Eric Godin, Paulo Tambasco de Oliveira, Gerald J Atkins, Antonio Nanci, Gethin Thomas. J Bone Miner Res 2008
109
68

A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V.
Tae-Joon Cho, Kyung-Eun Lee, Sook-Kyung Lee, Su Jeong Song, Kyung Jin Kim, Daehyun Jeon, Gene Lee, Ha-Neui Kim, Hye Ran Lee, Hye-Hyun Eom,[...]. Am J Hum Genet 2012
167
60

A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.
Oliver Semler, Lutz Garbes, Katharina Keupp, Daniel Swan, Katharina Zimmermann, Jutta Becker, Sandra Iden, Brunhilde Wirth, Peer Eysel, Friederike Koerber,[...]. Am J Hum Genet 2012
158
59

Type V osteogenesis imperfecta: a new form of brittle bone disease.
F H Glorieux, F Rauch, H Plotkin, L Ward, R Travers, P Roughley, L Lalic, D F Glorieux, F Fassier, N J Bishop. J Bone Miner Res 2000
279
47

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
74
40

Distinct patterns of IFITM-mediated restriction of filoviruses, SARS coronavirus, and influenza A virus.
I-Chueh Huang, Charles C Bailey, Jessica L Weyer, Sheli R Radoshitzky, Michelle M Becker, Jessica J Chiang, Abraham L Brass, Asim A Ahmed, Xiaoli Chi, Lian Dong,[...]. PLoS Pathog 2011
418
32


Phenotypic variability of osteogenesis imperfecta type V caused by an IFITM5 mutation.
Jay R Shapiro, Caressa Lietman, Monica Grover, James T Lu, Sandesh Cs Nagamani, Brian C Dawson, Dustin M Baldridge, Matthew N Bainbridge, Dan H Cohn, Maria Blazo,[...]. J Bone Miner Res 2013
53
45

The IFITM proteins mediate cellular resistance to influenza A H1N1 virus, West Nile virus, and dengue virus.
Abraham L Brass, I-Chueh Huang, Yair Benita, Sinu P John, Manoj N Krishnan, Eric M Feeley, Bethany J Ryan, Jessica L Weyer, Louise van der Weyden, Erol Fikrig,[...]. Cell 2009
900
31

Evolution of vertebrate interferon inducible transmembrane proteins.
Danielle Hickford, Stephen Frankenberg, Geoff Shaw, Marilyn B Renfree. BMC Genomics 2012
74
28

Genetic heterogeneity in osteogenesis imperfecta.
D O Sillence, A Senn, D M Danks. J Med Genet 1979
27

Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta.
Víctor Martínez-Glez, Maria Valencia, José A Caparrós-Martín, Mona Aglan, Samia Temtamy, Jair Tenorio, Veronica Pulido, Uschi Lindert, Marianne Rohrbach, David Eyre,[...]. Hum Mutat 2012
132
27

Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta.
Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno Jörn Bolz, Cecilia Giunta, Carsten Bergmann, Marianne Rohrbach, Friederike Koerber, Katharina Zimmermann,[...]. Am J Hum Genet 2011
227
25

New perspectives on osteogenesis imperfecta.
Antonella Forlino, Wayne A Cabral, Aileen M Barnes, Joan C Marini. Nat Rev Endocrinol 2011
385
25

Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta.
Helena E Christiansen, Ulrike Schwarze, Shawna M Pyott, Abdulrahman AlSwaid, Mohammed Al Balwi, Shatha Alrasheed, Melanie G Pepin, Mary Ann Weis, David R Eyre, Peter H Byers. Am J Hum Genet 2010
200
25

Natural history of hyperplastic callus formation in osteogenesis imperfecta type V.
Moira S Cheung, Francis H Glorieux, Frank Rauch. J Bone Miner Res 2007
51
37

Palmitoylome profiling reveals S-palmitoylation-dependent antiviral activity of IFITM3.
Jacob S Yount, Bruno Moltedo, Yu-Ying Yang, Guillaume Charron, Thomas M Moran, Carolina B López, Howard C Hang. Nat Chem Biol 2010
257
22

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.
Yasemin Alanay, Hrispima Avaygan, Natalia Camacho, G Eda Utine, Koray Boduroglu, Dilek Aktas, Mehmet Alikasifoglu, Ergul Tuncbilek, Diclehan Orhan, Filiz Tiker Bakar,[...]. Am J Hum Genet 2010
196
22

Ifitm3 limits the severity of acute influenza in mice.
Charles C Bailey, I-Chueh Huang, Christina Kam, Michael Farzan. PLoS Pathog 2012
164
22

The IFITM proteins inhibit HIV-1 infection.
Jennifer Lu, Qinghua Pan, Liwei Rong, Wei He, Shan-Lu Liu, Chen Liang. J Virol 2011
281
21

Normal germ line establishment in mice carrying a deletion of the Ifitm/Fragilis gene family cluster.
Ulrike C Lange, David J Adams, Caroline Lee, Sheila Barton, Robert Schneider, Allan Bradley, M Azim Surani. Mol Cell Biol 2008
95
21

Identification of five interferon-induced cellular proteins that inhibit west nile virus and dengue virus infections.
Dong Jiang, Jessica M Weidner, Min Qing, Xiao-Ben Pan, Haitao Guo, Chunxiao Xu, Xianchao Zhang, Alex Birk, Jinhong Chang, Pei-Yong Shi,[...]. J Virol 2010
256
21

IFITM3 inhibits influenza A virus infection by preventing cytosolic entry.
Eric M Feeley, Jennifer S Sims, Sinu P John, Christopher R Chin, Thomas Pertel, Li-Mei Chen, Gaurav D Gaiha, Bethany J Ryan, Ruben O Donis, Stephen J Elledge,[...]. PLoS Pathog 2011
268
21

Osteogenesis imperfecta.
Frank Rauch, Francis H Glorieux. Lancet 2004
768
21

WNT1 mutations in families affected by moderately severe and progressive recessive osteogenesis imperfecta.
Shawna M Pyott, Thao T Tran, Dru F Leistritz, Melanie G Pepin, Nancy J Mendelsohn, Renee T Temme, Bridget A Fernandez, Solaf M Elsayed, Ezzat Elsobky, Ishwar Verma,[...]. Am J Hum Genet 2013
145
21

Topological mapping of BRIL reveals a type II orientation and effects of osteogenesis imperfecta mutations on its cellular destination.
Alexa Patoine, Marie-Hélène Gaumond, Prashant K Jaiswal, François Fassier, Frank Rauch, Pierre Moffatt. J Bone Miner Res 2014
24
66

The small interferon-induced transmembrane genes and proteins.
Fredy Siegrist, Martin Ebeling, Ulrich Certa. J Interferon Cytokine Res 2011
114
20

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
Roy Morello, Terry K Bertin, Yuqing Chen, John Hicks, Laura Tonachini, Massimiliano Monticone, Patrizio Castagnola, Frank Rauch, Francis H Glorieux, Janice Vranka,[...]. Cell 2006
328
20

Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta.
Pablo Lapunzina, Mona Aglan, Samia Temtamy, José A Caparrós-Martín, Maria Valencia, Rocío Letón, Victor Martínez-Glez, Rasha Elhossini, Khalda Amr, Nuria Vilaboa,[...]. Am J Hum Genet 2010
176
20

IFITM3 restricts the morbidity and mortality associated with influenza.
Aaron R Everitt, Simon Clare, Thomas Pertel, Sinu P John, Rachael S Wash, Sarah E Smith, Christopher R Chin, Eric M Feeley, Jennifer S Sims, David J Adams,[...]. Nature 2012
521
20


Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation.
Ranad Shaheen, Anas M Alazami, Muneera J Alshammari, Eissa Faqeih, Nadia Alhashmi, Noon Mousa, Aisha Alsinani, Shinu Ansari, Fatema Alzahrani, Mohammed Al-Owain,[...]. J Med Genet 2012
92
20

Mutations in WNT1 cause different forms of bone fragility.
Katharina Keupp, Filippo Beleggia, Hülya Kayserili, Aileen M Barnes, Magdalena Steiner, Oliver Semler, Björn Fischer, Gökhan Yigit, Claudia Y Janda, Jutta Becker,[...]. Am J Hum Genet 2013
179
20

WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.
Christine M Laine, Kyu Sang Joeng, Philippe M Campeau, Riku Kiviranta, Kati Tarkkonen, Monica Grover, James T Lu, Minna Pekkinen, Maija Wessman, Terhi J Heino,[...]. N Engl J Med 2013
235
20

A nonclassical IFITM5 mutation located in the coding region causes severe osteogenesis imperfecta with prenatal onset.
Heike Hoyer-Kuhn, Oliver Semler, Lutz Garbes, Katharina Zimmermann, Jutta Becker, Bernd Wollnik, Eckhard Schoenau, Christian Netzer. J Bone Miner Res 2014
23
65

A novel IFITM5 mutation in severe atypical osteogenesis imperfecta type VI impairs osteoblast production of pigment epithelium-derived factor.
Charles R Farber, Adi Reich, Aileen M Barnes, Patricia Becerra, Frank Rauch, Wayne A Cabral, Alison Bae, Aaron Quinlan, Francis H Glorieux, Thomas L Clemens,[...]. J Bone Miner Res 2014
46
32

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
457
18

Genotype-phenotype study in type V osteogenesis imperfecta.
Meena Balasubramanian, Michael J Parker, Ann Dalton, Cecilia Giunta, Uschi Lindert, Luiz C Peres, Bart E Wagner, Paul Arundel, Amaka Offiah, Nicholas J Bishop. Clin Dysmorphol 2013
28
50

Phenotype and gene expression pattern of osteoblast-like cells cultured on polystyrene and hydroxyapatite with pre-adsorbed type-I collagen.
Nobutaka Hanagata, Taro Takemura, Akira Monkawa, Toshiyuki Ikoma, Junzo Tanaka. J Biomed Mater Res A 2007
25
52

Interferon-induced cell membrane proteins, IFITM3 and tetherin, inhibit vesicular stomatitis virus infection via distinct mechanisms.
Jessica M Weidner, Dong Jiang, Xiao-Ben Pan, Jinhong Chang, Timothy M Block, Ju-Tao Guo. J Virol 2010
227
17

PPIB mutations cause severe osteogenesis imperfecta.
Fleur S van Dijk, Isabel M Nesbitt, Eline H Zwikstra, Peter G J Nikkels, Sander R Piersma, Silvina A Fratantoni, Connie R Jimenez, Margriet Huizer, Alice C Morsman, Jan M Cobben,[...]. Am J Hum Genet 2009
183
17

Mutations in SERPINF1 cause osteogenesis imperfecta type VI.
Erica P Homan, Frank Rauch, Ingo Grafe, Caressa Lietman, Jennifer A Doll, Brian Dawson, Terry Bertin, Dobrawa Napierala, Roy Morello, Richard Gibbs,[...]. J Bone Miner Res 2011
116
17

The dispanins: a novel gene family of ancient origin that contains 14 human members.
Markus Sällman Almén, Nathalie Bringeland, Robert Fredriksson, Helgi B Schiöth. PLoS One 2012
63
20

Role of S-palmitoylation on IFITM5 for the interaction with FKBP11 in osteoblast cells.
Takashi Tsukamoto, Xianglan Li, Hiromi Morita, Takashi Minowa, Tomoyasu Aizawa, Nobutaka Hanagata, Makoto Demura. PLoS One 2013
24
54

Two mutations in IFITM5 causing distinct forms of osteogenesis imperfecta.
Encarna Guillén-Navarro, María Juliana Ballesta-Martínez, María Valencia, Ana María Bueno, Victor Martinez-Glez, Vanesa López-González, Birute Burnyte, Algirdas Utkus, Pablo Lapunzina, Victor L Ruiz-Perez. Am J Med Genet A 2014
28
46

Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expression.
Adi Reich, Alison S Bae, Aileen M Barnes, Wayne A Cabral, Aleksander Hinek, Jennifer Stimec, Suvimol C Hill, David Chitayat, Joan C Marini. J Clin Endocrinol Metab 2015
25
52

A transgenic mouse model of OI type V supports a neomorphic mechanism of the IFITM5 mutation.
Caressa D Lietman, Ronit Marom, Elda Munivez, Terry K Bertin, Ming-Ming Jiang, Yuqing Chen, Brian Dawson, Mary Ann Weis, David Eyre, Brendan Lee. J Bone Miner Res 2015
25
52

Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.
Wayne A Cabral, Weizhong Chang, Aileen M Barnes, MaryAnn Weis, Melissa A Scott, Sergey Leikin, Elena Makareeva, Natalia V Kuznetsova, Kenneth N Rosenbaum, Cynthia J Tifft,[...]. Nat Genet 2007
282
16

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
145
16

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
203
16


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.