Collagen and bone strength AL Boskey, TM Wright, RD Blank Journal of Bone and Mineral Research 14 (3), 330-335, 1999 | 266 | 1999 |
Secondary fracture prevention: consensus clinical recommendations from a multistakeholder coalition RB Conley, G Adib, RA Adler, KE Åkesson, IM Alexander, KC Amenta, ... Journal of bone and mineral research 35 (1), 36-52, 2020 | 232 | 2020 |
Congenital and idiopathic scoliosis: clinical and genetic aspects PF Giampietro, RD Blank, CL Raggio, S Merchant, FS Jacobsen, ... Clinical Medicine & Research 1 (2), 125-136, 2003 | 191 | 2003 |
Clinical, genetic and environmental factors associated with congenital vertebral malformations PF Giampietro, CL Raggio, RD Blank, C McCarty, U Broeckel, MA Pickart Molecular syndromology 4 (1-2), 94-105, 2013 | 131 | 2013 |
A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups D Londono, I Kou, TA Johnson, S Sharma, Y Ogura, T Tsunoda, ... Journal of medical genetics 51 (6), 401-406, 2014 | 92 | 2014 |
An analysis of PAX1 in the development of vertebral malformations PF Giampietro, CL Raggio, CE Reynolds, SK Shukla, E McPherson, ... Clinical genetics 68 (5), 448-453, 2005 | 92 | 2005 |
Spontaneous recombinase activity of Cre–ERT2 in vivo J Kristianto, MG Johnson, RK Zastrow, AB Radcliff, RD Blank Transgenic research 26, 411-417, 2017 | 86 | 2017 |
Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans PF Giampietro, SL Dunwoodie, K Kusumi, O Pourquié, O Tassy, AC Offiah, ... Annals of the New York Academy of Sciences 1151 (1), 38-67, 2009 | 83 | 2009 |
Osteoporosis in crisis: it's time to focus on fracture N Binkley, RD Blank, WD Leslie, EM Lewiecki, JA Eisman, JP Bilezikian Journal of Bone and Mineral Research 32 (7), 1391-1394, 2017 | 82 | 2017 |
A linkage map of mouse chromosome 12: localization of Igh and effects of sex and interference on recombination. RD Blank, GR Campbell, A Calabro, P D'Eustachio Genetics 120 (4), 1073-1083, 1988 | 82 | 1988 |
Synteny‐defined candidate genes for congenital and idiopathic scoliosis PF Giampietro, CL Raggio, RD Blank American journal of medical genetics 83 (3), 164-177, 1999 | 80 | 1999 |
Spectroscopically determined collagen Pyr/deH-DHLNL cross-link ratio and crystallinity indices differ markedly in recombinant congenic mice with divergent calculated bone … RD Blank, TH Baldini, M Kaufman, S Bailey, R Gupta, Y Yershov, ... Connective tissue research 44 (3-4), 134-142, 2003 | 76 | 2003 |
A novel locus for adolescent idiopathic scoliosis on chromosome 12p CL Raggio, PF Giampietro, S Dobrin, C Zhao, D Dorshorst, ... Journal of Orthopaedic Research 27 (10), 1366-1372, 2009 | 75 | 2009 |
A Missense T(Brachyury) Mutation Contributes to Vertebral Malformations N Ghebranious, RD Blank, CL Raggio, J Staubli, E McPherson, L Ivacic, ... Journal of bone and mineral research 23 (10), 1576-1583, 2008 | 73 | 2008 |
Advances in the nutritional and pharmacological management of phenylketonuria DM Ney, RD Blank, KE Hansen Current Opinion in Clinical Nutrition & Metabolic Care 17 (1), 61-68, 2014 | 72 | 2014 |
Clinical value of monitoring BMD in patients treated with bisphosphonates for osteoporosis NB Watts, EM Lewiecki, SL Bonnick, AJ Laster, N Binkley, RD Blank, ... Journal of Bone and Mineral Research 24 (10), 1643-1646, 2009 | 72 | 2009 |
Induced ablation of Bmp1 and Tll1 produces osteogenesis imperfecta in mice AM Muir, Y Ren, DH Butz, NA Davis, RD Blank, DE Birk, SJ Lee, D Rowe, ... Human molecular genetics 23 (12), 3085-3101, 2014 | 71 | 2014 |
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene … J Liu, N Wu, ... Genetics in Medicine 21 (7), 1548-1558, 2019 | 64 | 2019 |
Hexa‐D‐arginine treatment increases 7B2•PC2 activity in hyp‐mouse osteoblasts and rescues the HYP phenotype B Yuan, JQ Feng, S Bowman, Y Liu, RD Blank, I Lindberg, MK Drezner Journal of bone and mineral research 28 (1), 56-72, 2013 | 64 | 2013 |
Low bone strength is a manifestation of phenylketonuria in mice and is attenuated by a glycomacropeptide diet P Solverson, SG Murali, SJ Litscher, RD Blank, DM Ney Public Library of Science 7 (9), e45165, 2012 | 62 | 2012 |