M. Econs

发表

Disorders of phosphate metabolism.

L. Dimeglio, K. White, M. Econs, 2000, Endocrinology and metabolism clinics of North America.

Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche

Andrew D. Johnson, Daniel L. Koller, E. Demerath, 2014, Nature.

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Daniel L. Koller, David M. Evans, D. Kiel, 2012, Nature Genetics.

Editorial: The genetics of absorptive hypercalciuria - A note of caution

T. Foroud, M. Econs, 2002 .

The genetics of absorptive hypercalciuria--a note of caution.

T. Foroud, M. Econs, 2002, The Journal of clinical endocrinology and metabolism.

Familial Hypophosphatemia and Related Disorders

M. Econs, I. Holm, T. Carpenter, 2012 .

Genetic Disorders of Phosphate Homeostasis

K. White, M. Econs, F. R. Bringhurst, 2010 .

The roles of specific genes implicated as circulating factors involved in normal and disordered phosphate homeostasis: frizzled related protein-4, matrix extracellular phosphoglycoprotein, and fibroblast growth factor 23.

K. White, M. Econs, T. Larsson, 2006, Endocrine reviews.

Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23.

T. Strom, K. White, M. Econs, 2001, Kidney international.

Genetic Variants Associated with Circulating Fibroblast Growth Factor 23.

B. Kestenbaum, C. Robinson-Cohen, I. D. de Boer, 2018, Journal of the American Society of Nephrology : JASN.

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

Stephen C. J. Parker, Daniel L. Koller, D. Kiel, 2017, Nature Communications.

FGF23 is processed by proprotein convertases but not by PHEX.

T. Strom, H. Zischka, K. White, 2004, Bone.

A novel GALNT3 mutation in a pseudoautosomal dominant form of tumoral calcinosis: evidence that the disorder is autosomal recessive.

M. Econs, K. Lyles, S. Ichikawa, 2005, The Journal of clinical endocrinology and metabolism.

A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.

K. White, M. Econs, M. Mohammadi, 2007, Journal of musculoskeletal & neuronal interactions.

Novel GALNT3 mutations causing hyperostosis-hyperphosphatemia syndrome result in low intact fibroblast growth factor 23 concentrations.

M. Econs, B. Petit, J. Henley, 2007, The Journal of clinical endocrinology and metabolism.

Ablation of the Galnt3 gene leads to low-circulating intact fibroblast growth factor 23 (Fgf23) concentrations and hyperphosphatemia despite increased Fgf23 expression.

T. A. Fritz, M. Econs, S. Hui, 2009, Endocrinology.

Genetic loci affecting bone structure and strength in inbred COP and DA rats.

Daniel L. Koller, T. Foroud, M. Econs, 2008, Bone.

Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria.

M. Econs, S. Ichikawa, J. Gertner, 2006, The Journal of clinical endocrinology and metabolism.

Epistasis between QTLs for bone density variation in Copenhagen × dark agouti F2 rats

Daniel L. Koller, T. Foroud, M. Econs, 2009, Mammalian Genome.

Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia.

K. White, M. Econs, H. Jüppner, 2003, The New England journal of medicine.

Meta‐analysis of genome‐wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

Daniel L. Koller, D. Kiel, T. Spector, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Osteoblast-Specific Overexpression of Human WNT16 Increases Both Cortical and Trabecular Bone Mass and Structure in Mice.

M. Econs, A. Robling, K. Lim, 2016, Endocrinology.

Whole‐Genome Scan for Linkage to Bone Strength and Structure in Inbred Fischer 344 and Lewis Rats

Daniel L. Koller, T. Foroud, M. Econs, 2005, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

X-linked hypophosphatemic rickets without “rickets”

G. Samsa, J. Feussner, M. Econs, 1991, Skeletal Radiology.

Phenotypic and Genotypic Characterization and Treatment of a Cohort With Familial Tumoral Calcinosis/Hyperostosis‐Hyperphosphatemia Syndrome

K. White, M. Econs, Marcus Y. Chen, 2016, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Tumoral calcinosis presenting with eyelid calcifications due to novel missense mutations in the glycosyl transferase domain of the GALNT3 gene.

M. Econs, P. Knudson, S. Ichikawa, 2006, The Journal of clinical endocrinology and metabolism.

Common genetic determinants of vitamin D insufficiency

Daniel L. Koller, P. O’Reilly, D. Kiel, 2011 .

Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck.

Daniel L. Koller, T. Foroud, M. Econs, 2008, Physiological genomics.

Bone loss at the femoral neck in premenopausal white women: effects of weight change and sex-hormone levels.

C. Longcope, M. Econs, A. Perkins, 2002, The Journal of clinical endocrinology and metabolism.

Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene.

T. Meitinger, T. Strom, B. Lorenz, 2000, Gene.

Osteoclast-derived serum tartrate-resistant acid phosphatase 5b in Albers-Schonberg disease (type II autosomal dominant osteopetrosis).

M. Econs, S. Waguespack, H. Väänänen, 2004, Clinical chemistry.

Sensitivity of fibroblast growth factor 23 measurements in tumor-induced osteomalacia.

M. Econs, D. Shulman, M. Peacock, 2006, The Journal of clinical endocrinology and metabolism.

Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation.

K. White, M. Econs, D. Fitzpatrick, 2005, American journal of human genetics.

Phosphaturic mesenchymal tumor, mixed connective tissue variant, of the mandible: report of a case and review of the literature.

A. Folpe, M. Econs, R. Landesberg, 2009, Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.

Measurement of tartrate-resistant acid phosphatase and the brain isoenzyme of creatine kinase accurately diagnoses type II autosomal dominant osteopetrosis but does not identify gene carriers.

K. White, M. Econs, S. Hui, 2002, The Journal of clinical endocrinology and metabolism.

Novel PHEX gene locus‐specific database: Comprehensive characterization of vast number of variants associated with X‐linked hypophosphatemia (XLH)

S. Daugherty, R. Truty, M. Econs, 2021, Human mutation.

Hypophosphatemic Rickets

L. Dimeglio, M. Econs, 2004, Reviews in Endocrine and Metabolic Disorders.

Genetic diseases resulting from disordered FGF23/klotho biology.

M. Econs, 2017, Bone.

Dietary phosphate restriction normalizes biochemical and skeletal abnormalities in a murine model of tumoral calcinosis.

M. Econs, M. Allen, S. Ichikawa, 2011, Endocrinology.

Establishment of sandwich ELISA for soluble alpha-Klotho measurement: Age-dependent change of soluble alpha-Klotho levels in healthy subjects.

M. Econs, Y. Nabeshima, N. Okamoto, 2010, Biochemical and biophysical research communications.

Familial tumoral calcinosis is characterized by ectopic calcifications and hyperphosphatemia due to inactivating mutations in FGF 23 or UDP-N-acetyl-α-D-galactosamine : polypeptide

K. White, M. Econs, M. Mohammadi, 2007 .

Overexpression of WNT16 Does Not Prevent Cortical Bone Loss Due to Glucocorticoid Treatment in Mice

M. Econs, T. Bellido, Rita L. Gerard-O’Riley, 2018, JBMR plus.

Clinical vignette: osteopathia striata with cranial sclerosis.

M. Econs, E. Braunstein, C. Lazar, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Osteopathia Striata with Cranial Sclerosis

M. Econs, E. Braunstein, C. Lazar, 1999 .

Iron modifies plasma FGF23 differently in autosomal dominant hypophosphatemic rickets and healthy humans.

Leah R. Padgett, M. Econs, M. Peacock, 2011, The Journal of clinical endocrinology and metabolism.

Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets.

M. Econs, E. Traxler, S. Ichikawa, 2008, Bone.

The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting.

T. Spector, T. Meitinger, T. Strom, 2001, The Journal of clinical endocrinology and metabolism.

Discordance for X-Linked Hypophosphataemic Rickets in Identical Twin Girls

M. Econs, S. Pearce, T. Cheetham, 2009, Hormone Research in Paediatrics.

Diagnosis and Management of Osteopetrosis: Consensus Guidelines From the Osteopetrosis Working Group

L. Dimeglio, M. Econs, D. Shoback, 2017, The Journal of clinical endocrinology and metabolism.

Resolution of severe, adolescent-onset hypophosphatemic rickets following resection of an FGF-23-producing tumour of the distal ulna.

F. Glorieux, K. White, M. Econs, 2004, Bone.

CHAPTER 70 – Disorders of Phosphate Metabolism: Autosomal Dominant Hypophosphatemic Rickets, Tumor Induced Osteomalacia, Fibrous Dysplasia, and the Pathophysiological Relevance of FGF23

M. Econs, 2005 .

Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations

Leah R. Padgett, M. Econs, P. Quartier, 2010, American journal of medical genetics. Part A.

A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.

K. White, M. Econs, M. Mohammadi, 2007, The Journal of clinical investigation.

Oral Iron Replacement Normalizes Fibroblast Growth Factor 23 in Iron‐Deficient Patients With Autosomal Dominant Hypophosphatemic Rickets

M. Econs, Ziyue Liu, R. Mehta, 2020, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Severe FGF23-based hypophosphataemic osteomalacia due to ferric carboxymaltose administration

M. Econs, J. Rubin, Klara R. Klein, 2018, BMJ Case Reports.

Hypophosphatemic Rickets: Revealing Novel Control Points for Phosphate Homeostasis

K. White, M. Econs, J. Hum, 2014, Current Osteoporosis Reports.

Fibroblast growth factor 23: roles in health and disease.

M. Econs, E. Imel, 2005, Journal of the American Society of Nephrology : JASN.

FGF-23 is elevated by chronic hyperphosphatemia.

M. Econs, M. Collins, S. Marx, 2004, The Journal of clinical endocrinology and metabolism.

Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies

E. Farrow, M. Econs, M. Collins, 2018, The Journal of clinical investigation.

Normal calcitonin stimulation of serum calcitriol in patients with X-linked hypophosphatemic rickets.

M. Econs, M. Drezner, B. Lobaugh, 1992, The Journal of clinical endocrinology and metabolism.

Effects of Iron Isomaltoside vs Ferric Carboxymaltose on Hypophosphatemia in Iron-Deficiency Anemia: Two Randomized Clinical Trials.

M. Wolf, M. Econs, J. Rubin, 2020, JAMA.

A Phex mutation in a murine model of X‐linked hypophosphatemia alters phosphate responsiveness of bone cells

M. Econs, S. Ichikawa, Anthony M. Austin, 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Inherited Phosphate Wasting Disorders

K. White, M. Econs, 2000 .

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

A. Poustka, T. Meitinger, T. Strom, 1995, Nature Genetics.

The discovery of FGF23—a historic view

M. Econs, Farah Laith Al Sabie, Farah Al Sabie, 2021 .

FGF23 and the Regulation of Phosphorus Metabolism

K. White, M. Econs, 2018, Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism.

A Mutation in the Dmp1 Gene Alters Phosphate Responsiveness in Mice

M. Econs, Jian Q. Feng, S. Ichikawa, 2017, Endocrinology.

Fibroblast Growth Factor‐23 (FGF23)

K. White, M. Econs, 2013 .

Dosage Effect of a Phex Mutation in a Murine Model of X-Linked Hypophosphatemia

M. Econs, S. Ichikawa, E. Bikorimana, 2013, Calcified Tissue International.

Introduction to skeletal genetics.

M. Econs, 2008, Journal of musculoskeletal & neuronal interactions.

Hypophosphatemia, osteomalacia and proximal muscle weakness treated by surgery.

K. White, M. Econs, A. Hermus, 2003, Clinical endocrinology.

New insights into the pathogenesis of inherited phosphate wasting disorders.

M. Econs, 1999, Bone.

Phosphate transport in immortalized cell cultures from the renal proximal tubule of normal and Hyp Mice: Evidence That the HYP gene locus product is an extrarenal factor

M. Econs, H. Tenenhouse, M. Drezner, 1995, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A YAC contig spanning the hypophosphatemic rickets disease gene (HYP) candidate region.

C. G. See, H. Lehrach, M. Econs, 1994, Genomics.

Conventional Therapy in Adults With XLH Improves Dental Manifestations, But Not Enthesopathy.

M. Econs, 2015, The Journal of clinical endocrinology and metabolism.

Iron and fibroblast growth factor 23 in X-linked hypophosphatemia.

Leah R. Padgett, M. Econs, E. Imel, 2014, Bone.

Serum fibroblast growth factor 23, serum iron and bone mineral density in premenopausal women.

Leah R. Padgett, M. Econs, M. Peacock, 2016, Bone.

Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels

Peter K. Joshi, P. O’Reilly, M. Jarvelin, 2018, Nature Communications.

Common genetic determinants of vitamin D insufficiency: a genome-wide association study

Daniel L. Koller, P. O’Reilly, D. Kiel, 2010, The Lancet.

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes.

Daniel L. Koller, T. Foroud, M. Econs, 2005, Bone.

Persistent tumor-induced osteomalacia confirmed by elevated postoperative levels of serum fibroblast growth factor-23 and 5-year follow-up of bone density changes.

K. White, M. Econs, Felice A Caldarella, 2005, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate Wasting

T. Spector, T. Meitinger, T. Strom, 2001 .

Chapter 23. Fibroblast Growth Factor‐23

K. White, M. Econs, 2009 .

Osteoglophonic dysplasia: A ‘common’ mutation in a rare disease

M. Econs, C. Siar, Z. Latiff, 2010, Clinical genetics.

Osteopetroses, emphasizing potential approaches to treatment.

M. Econs, A. Teti, 2017, Bone.

Unusual Cortical Phenotype After Hematopoietic Stem Cell Transplantation in a Patient With Osteopetrosis

M. Econs, S. Warden, P. Orchard, 2022, JBMR plus.

Locus heterogeneity of autosomal dominant osteopetrosis (ADO).

T. Foroud, K. White, M. Econs, 1999, The Journal of clinical endocrinology and metabolism.

Genetic rescue of glycosylation-deficient Fgf23 in the Galnt3 knockout mouse.

Leah R. Padgett, K. White, M. Econs, 2014, Endocrinology.

Dosage Effect of a Phex Mutation in a Murine Model of X-Linked Hypophosphatemia

M. Econs, S. Ichikawa, E. Bikorimana, 2013, Calcified Tissue International.

Case 29-2001: oncogenic hypophosphatemic osteomalacia.

K. White, M. Econs, S. Waguespack, 2002, The New England journal of medicine.

Genetics of familial tumoral calcinosis.

M. Econs, S. Ichikawa, E. Imel, 2009, American journal of kidney diseases : the official journal of the National Kidney Foundation.

FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wasting.

K. White, M. Econs, M. Collins, 2003, The Journal of clinical investigation.

Radiographic imaging, densitometry and disease severity in Autosomal dominant osteopetrosis type 2

M. Econs, S. Warden, Ziyue Liu, 2020, Skeletal Radiology.

MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia.

K. White, M. Econs, R. Dong, 2000, Genomics.

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

T. Meitinger, T. Strom, K. White, 2000, Nature Genetics.

Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder.

M. Econs, P. Mcenery, Michael J. Econs, 1997, The Journal of clinical endocrinology and metabolism.

Approach to the hypophosphatemic patient.

M. Econs, Michael J Econs, Erik A Imel, 2012, The Journal of clinical endocrinology and metabolism.

Tumor-induced osteomalacia--unveiling a new hormone.

M. Econs, M. Drezner, Michael J. Econs, 1994, The New England journal of medicine.

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Christian Gieger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.

SIBLING family genes and bone mineral density: association and allele-specific expression in humans.

Leah R. Padgett, Daniel L. Koller, T. Foroud, 2014, Bone.

Positional cloning of the HYP gene: a review.

M. Econs, 1996, Kidney international.

Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets.

T. Meitinger, T. Strom, H. Lehrach, 1997, Genome research.

Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment

Matthew A. Hibbs, Daniel L. Koller, A. Hofman, 2014, PLoS genetics.

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 11p12-13.

Daniel L. Koller, T. Foroud, M. Econs, 2002, The Journal of clinical endocrinology and metabolism.

Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/type IIc sodium-phosphate cotransporter: presentation as hypercalciuria and nephrolithiasis.

M. Econs, E. McCarthy, M. Levine, 2009, The Journal of clinical endocrinology and metabolism.

Most Osteomalacia-associated Mesenchymal Tumors Are a Single Histopathologic Entity: An Analysis of 32 Cases and a Comprehensive Review of the Literature

E. Montgomery, A. Folpe, J. O'Connell, 2004, The American journal of surgical pathology.

Renal phosphate wasting disorders: clinical features and pathogenesis.

K. White, M. Econs, Lori A Brame, 2004, Seminars in nephrology.

Disentangling the genetics of lean mass.

Daniel L. Koller, D. Kiel, C. Gieger, 2019, The American journal of clinical nutrition.

Fine mapping of bone structure and strength QTLs in heterogeneous stock rat.

Daniel L. Koller, T. Foroud, T. Olsson, 2015, Bone.

Bone marrow transplantation as a therapy for autosomal dominant osteopetrosis type 2 in mice

M. Econs, E. Srour, M. Kacena, 2022, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Interferon Gamma‐1b Does Not Increase Markers of Bone Resorption in Autosomal Dominant Osteopetrosis

M. Econs, Ziyue Liu, E. Imel, 2019, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Interferon Gamma, but not Calcitriol Improves the Osteopetrotic Phenotypes in ADO2 Mice

M. Econs, Rita L. Gerard-O’Riley, I. Alam, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

High‐Resolution Genome Screen for Bone Mineral Density in Heterogeneous Stock Rat

Daniel L. Koller, T. Foroud, T. Olsson, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Hyperphosphatemic Tumoral Calcinosis With Pemigatinib Use

M. Econs, P. Helft, Matthew F. Kuhar, 2022, AACE clinical case reports.

Explorer Mutations that cause osteoglophonic dysplasia define novel roles for FGFR 1 in bone elongation

K. White, M. Econs, D. Fitzpatrick, 2017 .

Genetic Variants Associated with Circulating Parathyroid Hormone.

Daniel L. Koller, J. Pankow, A. Paterson, 2017, Journal of the American Society of Nephrology : JASN.

Parent-of-Origin Specific Allelic Associations Among 106 Genomic Loci for Age at Menarche

Andrew D. Johnson, Daniel L. Koller, E. Demerath, 2014 .

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women.

Leah R. Padgett, Daniel L. Koller, K. Doheny, 2010, The Journal of clinical endocrinology and metabolism.

Genetics of osteoporosis.

Tatiana Foroud, T. Foroud, M. Econs, 2002, Endocrine reviews.

Meta‐Analysis of Genome‐Wide Scans Provides Evidence for Sex‐ and Site‐Specific Regulation of Bone Mass

Daniel L. Koller, D. Kiel, A. Uitterlinden, 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry

Daniel L. Koller, D. Kiel, A. Uitterlinden, 2019, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Autosomal dominant osteopetrosis: clinical severity and natural history of 94 subjects with a chloride channel 7 gene mutation.

L. Dimeglio, M. Econs, S. Hui, 2007, The Journal of clinical endocrinology and metabolism.

Chloride Channel 7 (ClCN7) Gene Mutations and Autosomal Dominant Osteopetrosis, Type II

Daniel L. Koller, T. Foroud, K. White, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Autosomal dominant osteopetrosis.

M. Econs, L. Polgreen, E. Imel, 2023, Bone.

Phenotypic severity of autosomal dominant osteopetrosis type II (ADO2) mice on different genetic backgrounds recapitulates the features of human disease.

M. Econs, Rita L. Gerard-O’Riley, I. Alam, 2017, Bone.

A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.

T. Strom, M. Econs, F. Francis, 1998, The Journal of clinical endocrinology and metabolism.

Autosomal dominant hyperostosis/osteosclerosis with high serum alkaline phosphatase activity.

M. Econs, G. Howard, B. Roos, 2003, The Journal of clinical endocrinology and metabolism.

Fibrous dysplasia, phosphate wasting and fibroblast growth factor 23.

M. Econs, E. Imel, 2007, Pediatric endocrinology reviews : PER.

Chromosomal Localization of Two Human Genes Involved in Phosphate Homeostasis: The Type IIb Sodium-Phosphate Cotransporter and Stanniocalcin-2

K. White, M. Econs, H. Murer, 1998, Somatic cell and molecular genetics.

Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35.

M. Econs, C. Kos, F. Tihy, 1994, Genomics.

Heterogeneous stock rat: a unique animal model for mapping genes influencing bone fragility.

Daniel L. Koller, J. Flint, T. Foroud, 2011, Bone.

A 2D crossover–based map of the human X chromosome as a model for map integration

M. Econs, D. Barker, P. Fain, 1995, Nature Genetics.

Genetics of Osteoporosis and Metabolic Bone Disease, The

M. Econs, 2000 .

The Genetics of Osteoporosis and Metabolic Bone Disease

M. Econs, 2000, Humana Press.

Efficient and stable gene expression into human osteoclasts using an HIV-1-based lentiviral vector.

K. Cornetta, M. Econs, K. Chu, 2008, DNA and cell biology.

False Positive Rates in Association Studies as a Function of Degree of Stratification

Tatiana Foroud, Daniel L. Koller, Michael J. Econs, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions

Yadong Wang, Yunlong Liu, Mingxiang Teng, 2012, Bioinform..

Rapid publication: Flanking markers define the X‐linked hypophosphatemic rickets gene locus

M. Pericak-Vance, M. Econs, D. Barker, 1993, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The Molecular Basis of Hypophosphatemic Rickets

T. Strom, M. Econs, 1999 .

Positional cloning of the PEX gene: new insights into the pathophysiology of X-linked hypophosphatemic rickets.

M. Econs, F. Francis, 1997, American journal of physiology. Renal physiology.

X-Linked hypophosphatemic rickets: a disease often unknown to affected patients.

G. Samsa, J. Feussner, M. Econs, 1994, Bone and mineral.

Peak bone mineral density at the hip is linked to chromosomes 14q and 15q

Daniel L. Koller, T. Foroud, M. Econs, 2004, Osteoporosis International.

Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).

T. Meitinger, T. Strom, H. Lehrach, 1997, Human molecular genetics.

Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia.

T. Meitinger, T. Strom, H. Lehrach, 1997, Human molecular genetics.

C 3 H 10 T 1 / 2 AND C 2 C 12

T. Takeda, L. Dimeglio, M. Econs, 2007 .

Mosaicism in osteopathia striata with cranial sclerosis.

M. Econs, S. Ichikawa, Dennis Joseph, 2010, The Journal of clinical endocrinology and metabolism.

Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and Women

Daniel L. Koller, T. Foroud, M. Econs, 2005, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women.

Shoji Ichikawa, Siu L Hui, Daniel L. Koller, 2005, The Journal of clinical endocrinology and metabolism.

Identification of Genes Influencing Skeletal Phenotypes in Congenic P/NP Rats

M. Econs, C. Turner, H. Edenberg, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Replication of Previous Genome-wide Association Studies of Bone Mineral Density in Premenopausal American Women

Leah R. Padgett, Daniel L. Koller, T. Foroud, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Sex‐Specific Genetic Loci for Femoral Neck Bone Mass and Strength Identified in Inbred COP and DA Rats

Daniel L. Koller, T. Foroud, M. Econs, 2008, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Contribution of the LRP5 Gene to Normal Variation in Peak BMD in Women

Daniel L. Koller, T. Foroud, M. Econs, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genome Screen for Quantitative Trait Loci Underlying Normal Variation in Femoral Structure

Daniel L. Koller, T. Foroud, M. Econs, 2001, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Treatment of X-linked hypophosphatemia with calcitriol and phosphate increases circulating fibroblast growth factor 23 concentrations.

L. Dimeglio, M. Econs, S. Hui, 2010, The Journal of clinical endocrinology and metabolism.

Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women

Daniel L. Koller, T. Foroud, M. Econs, 2006, Osteoporosis International.

Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women.

Siu L Hui, Daniel L. Koller, T. Foroud, 2004, American journal of human genetics.

Heritability of Changes in Bone Size and Bone Mass With Age in Premenopausal White Sisters

Daniel L. Koller, T. Foroud, M. Econs, 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Case 18-2022: A 29-Year-Old Woman with Recurrent Fractures.

M. Econs, Daryl J. Selen, O. Zurkiya, 2022, The New England journal of medicine.

Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues

T. Strom, M. Econs, A. Hanauer, 1999, European Journal of Human Genetics.

Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci.

Daniel L. Koller, T. Foroud, M. Econs, 2009, Bone.

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men.

Daniel L. Koller, T. Foroud, M. Econs, 2005, Bone.

The Case: Ectopic calcifications in a child

M. Econs, E. Imel, T. Jamale, 2014, Kidney international.

Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men.

Daniel L. Koller, T. Foroud, M. Econs, 2005, The Journal of clinical endocrinology and metabolism.

Bone Mass and Strength are Significantly Improved in Mice Overexpressing Human WNT16 in Osteocytes

M. Econs, A. Robling, K. Lim, 2017, Calcified Tissue International.

FGF-23 is a circulating factor that is elevated in oncogenic osteomalacia and X-linked hypophosphatemic rickets.

K. White, M. Econs, J. Lavigne, 2002 .

The gene for X-linked hypophosphataemic rickets maps to a 200–300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)

J. Weissenbach, H. Lehrach, K. Davies, 1996, Human Genetics.

Association of Adenylate Cyclase 10 (ADCY10) Polymorphisms and Bone Mineral Density in Healthy Adults

Daniel L. Koller, T. Foroud, M. Econs, 2009, Calcified Tissue International.

Chapter 62 – Genetic Disorders of Phosphate Homeostasis

K. White, M. Econs, F. R. Bringhurst, 2016 .

Dinucleotide repeat polymorphism at the DXS1683 locus.

H. Lehrach, M. Econs, F. Francis, 1994, Human Molecular Genetics.

Intronic deletions in the SLC34A3 gene: a cautionary tale for mutation analysis of hereditary hypophosphatemic rickets with hypercalciuria.

Leah R. Padgett, M. Econs, S. Ichikawa, 2014, Bone.

Tumor-induced rickets: usefulness of MR gradient echo recall imaging for tumor localization.

K. White, M. Econs, D. Shulman, 2004, The Journal of pediatrics.

Localization of PiUS, a stimulator of cellular phosphate uptake to human chromosome 3p21.3

K. White, M. Econs, 1998, Somatic cell and molecular genetics.

Genetics of osteoporosis.

T. Foroud, M. Econs, C. Turner, 2002, Endocrine reviews.

Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains

Daniel L. Koller, T. Foroud, M. Econs, 2005, Mammalian Genome.

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Andrew D. Johnson, Daniel L. Koller, E. Demerath, 2010 .

Generation of the first autosomal dominant osteopetrosis type II (ADO2) disease models.

M. Econs, K. Mohammad, M. Capulli, 2014, Bone.

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Andrew D. Johnson, Daniel L. Koller, E. Demerath, 2010 .

Genome-wide association study of serum iron phenotypes in premenopausal women of European descent.

Leah R. Padgett, Daniel L. Koller, T. Foroud, 2016, Blood cells, molecules & diseases.

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men.

Daniel L. Koller, T. Foroud, M. Econs, 2008, Bone.

Disease Status in Autosomal Dominant Osteopetrosis Type 2 Is Determined by Osteoclastic Properties

M. Econs, K. Chu, Richard Snyder, 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

Stephen C. J. Parker, Daniel L. Koller, D. Kiel, 2017, Nature Communications.

Genetics of osteoporosis.

T. Foroud, M. Econs, C. Turner, 2002, Endocrine reviews.

Meta‐analysis of genome‐wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

Daniel L. Koller, D. Kiel, T. Spector, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

SIBLING family genes and bone mineral density: association and allele-specific expression in humans.

Leah R. Padgett, Daniel L. Koller, T. Foroud, 2014, Bone.

Heterogeneous stock rat: a unique animal model for mapping genes influencing bone fragility.

Daniel L. Koller, J. Flint, T. Foroud, 2011, Bone.

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men.

Daniel L. Koller, T. Foroud, M. Econs, 2008, Bone.

Osteopetrosis: pathogenesis, management and future directions for research

M. Econs, M. Levine, D. Weber, 2014 .

Meta‐Analysis of Genome‐Wide Scans Provides Evidence for Sex‐ and Site‐Specific Regulation of Bone Mass

Daniel L. Koller, D. Kiel, T. Spector, 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Fibroblast growth factor 23: roles in health and disease.

M. Econs, E. Imel, 2005, Journal of the American Society of Nephrology : JASN.