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Robert D Blank
Robert D Blank
Professor Emeritus of Medicine, Medical College of Wisconsin
Verified email at mcw.edu
Title
Cited by
Cited by
Year
Collagen and bone strength
AL Boskey, TM Wright, RD Blank
Journal of Bone and Mineral Research 14 (3), 330-335, 1999
2621999
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
2262020
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
1892003
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
1262013
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
912014
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
912005
Spontaneous recombinase activity of Cre–ERT2 in vivo
J Kristianto, MG Johnson, RK Zastrow, AB Radcliff, RD Blank
Transgenic research 26, 411-417, 2017
862017
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
822009
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
821988
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
812017
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
801999
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
752009
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
742003
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
722009
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
722008
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
712014
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
712014
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
622019
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
622013
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
592012
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