Disease status in autosomal dominant osteopetrosis type 2 is determined by osteoclastic propertiesKANG CHU; SNYDER, Richard; ECONS, Michael J et al.Journal of bone and mineral research (Print). 2006, Vol 21, Num 7, pp 1089-1097, issn 0884-0431, 9 p.Article

Fibroblast growth factor 23 : Roles in health and diseaseIMEL, Erik A; ECONS, Michael J.Journal of the American Society of Nephrology. 2005, Vol 16, Num 9, pp 2565-2575, issn 1046-6673, 11 p.Article

Approach to the Hypophosphatemic PatientIMEL, Erik A; ECONS, Michael J.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 3, pp 696-706, issn 0021-972X, 11 p.Article

Genetics of osteoporosisPEACOCK, Munro; TURNER, Charles H; ECONS, Michael J et al.Endocrine reviews. 2002, Vol 23, Num 3, pp 303-326, issn 0163-769XArticle

Dietary Phosphate Restriction Normalizes Biochemical and Skeletal Abnormalities in a Murine Model of Tumoral CalcinosisICHIKAWA, Shoji; AUSTIN, Anthony M; GRAY, Amie K et al.Endocrinology (Philadelphia). 2011, Vol 152, Num 12, pp 4504-4513, issn 0013-7227, 10 p.Article

Autosomal dominant osteopetrosis : Clinical severity and natural history of 94 subjects with a chloride channel 7 gene mutationWAGUESPACK, Steven G; HUI, Siu L; DIMEGLIO, Linda A et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 3, pp 771-778, issn 0021-972X, 8 p.Article

A Phex Mutation in a Murine Model of X-Linked Hypophosphatemia Alters Phosphate Responsiveness of Bone CellsICHIKAWA, Shoji; AUSTIN, Anthony M; GRAY, Amie K et al.Journal of bone and mineral research (Print). 2012, Vol 27, Num 2, pp 453-460, issn 0884-0431, 8 p.Article

False positive rates in association studies as a function of degree of stratificationKOLLER, Daniel L; PEACOCK, Munro; DONGBING LAI et al.Journal of bone and mineral research (Print). 2004, Vol 19, Num 8, pp 1291-1295, issn 0884-0431, 5 p.Article

Disorders of phosphate metabolismDIMEGLIO, Linda A; WHITE, Kenneth E; ECONS, Michael J et al.Endocrinology and metabolism clinics of North America. 2000, Vol 29, Num 3, pp vii-viii, issn 0889-8529, 21 p.Article

Iron and fibroblast growth factor 23 in X-linked hypophosphatemiaIMEL, Erik A; GRAY, Amie K; PADGETT, Leah R et al.Bone (New York, NY). 2014, Vol 60, pp 87-92, issn 8756-3282, 6 p.Article

Heterogeneous stock rat: A unique animal model for mapping genes influencing bone fragilityALAM, Imranul; KOLLER, Daniel L; DIAZ, Sira et al.Bone (New York, NY). 2011, Vol 48, Num 5, pp 1169-1177, issn 8756-3282, 9 p.Article

Identification of a Linkage Disequilibrium Block in Chromosome 1q Associated With BMD in Premenopausal White WomenICHIKAWA, Shoji; KOLLER, Daniel L; FOROUD, Tatiana et al.Journal of bone and mineral research (Print). 2008, Vol 23, Num 10, pp 1680-1688, issn 0884-0431, 9 p.Article

Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuriaICHIKAWA, Shoji; SORENSON, Andrea H; IMEL, Erik A et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 10, pp 4022-4027, issn 0021-972X, 6 p.Article

Analysis of variation in expression of autosomal dominant osteopetrosis type 2 : Searching for modifier genesKANG CHU; KOLLER, Daniel L; SNYDER, Richard et al.Bone (New York, NY). 2005, Vol 37, Num 5, pp 655-661, issn 8756-3282, 7 p.Article

The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wastingWHITE, Kenneth E; JONSSON, Kenneth B; MEITINGER, Thomas et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 2, pp 497-500, issn 0021-972XArticle

Generation of the first autosomal dominant osteopetrosis type II (ADO2) disease modelsALAM, Imranul; GRAY, Amie K; ECONS, Michael J et al.Bone (New York, NY). 2014, Vol 59, pp 66-75, issn 8756-3282, 10 p.Article

Clinical Variability of Familial Tumoral Calcinosis Caused by Novel GALNT3 MutationsICHIKAWA, Shoji; BAUJAT, Geneviève; QUARTIER, Pierre et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 4, pp 896-903, issn 1552-4825, 8 p.Article

Genetic loci affecting bone structure and strength in inbred COP and DA ratsQIWEI SUN; ALAM, Imranul; LIXIANG LIU et al.Bone (New York, NY). 2008, Vol 42, Num 3, pp 547-553, issn 8756-3282, 7 p.Article

Linkage Screen for BMD Phenotypes in Male and Female COP and DA Rat StrainsKOLLER, Daniel L; LIXIANG LIU; ALAM, Imranul et al.Journal of bone and mineral research (Print). 2008, Vol 23, Num 9, pp 1382-1388, issn 0884-0431, 7 p.Article

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white menCHU, Kang; KOLLER, Daniel L; FOROUD, Tatiana M et al.Bone (New York, NY). 2008, Vol 43, Num 6, pp 995-998, issn 8756-3282, 4 p.Article

Peak bone mineral density at the hip is linked to chromosomes 14q and 15qPEACOCK, Munro; KOLLER, Daniel L; SIU HUI et al.Osteoporosis international. 2004, Vol 15, Num 6, pp 489-496, issn 0937-941X, 8 p.Article

Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type IIWAGUESPACK, Steven G; KOLLER, Daniel L; ECONS, Michael J et al.Journal of bone and mineral research (Print). 2003, Vol 18, Num 8, pp 1513-1518, issn 0884-0431, 6 p.Article

Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13CARN, Gwenaelle; KOLLER, Daniel L; PEACOCK, Munro et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 8, pp 3819-3824, issn 0021-972XArticle

Identification of Genes Influencing Skeletal Phenotypes in Congenic P/NP RatsALAM, Imranul; CARR, Lucinda G; TIEBING LIANG et al.Journal of bone and mineral research (Print). 2010, Vol 25, Num 6, pp 1314-1325, issn 0884-0431, 12 p.Article

Heritability of changes in bone size and bone mass with age in premenopausal white sistersHUI, Siu L; KOLLER, Daniel L; FOROUD, Tatiana M et al.Journal of bone and mineral research (Print). 2006, Vol 21, Num 7, pp 1121-1125, issn 0884-0431, 5 p.Article