Millan S Patel

发表

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.

Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation.

Hans Clevers, Andrew P McMahon, Michael Starbuck, 2005, Developmental cell.

The Molecular Clock Mediates Leptin-Regulated Bone Formation

E. Wagner, A. Bradley, L. Fu, 2005, Cell.

Fatal Congenital Hypertrophic Cardiomyopathy and a Pancreatic Nodule Morphologically Identical to Focal Lesion of Congenital Hyperinsulinism in an Infant with Costello Syndrome: Case Report and Review of the Literature

S. Yip, Millan S Patel, E. Ruchelli, 2015, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Competing Factors Link to Bone Health in Polycystic Ovary Syndrome: Chronic Low-Grade Inflammation Takes a Toll

E. Kingwell, J. Prior, Millan S Patel, 2017, Scientific Reports.

Osteoporotic fractures and obesity affect frailty progression: a longitudinal analysis of the Canadian multicentre osteoporosis study

Jacques P. Brown, P. Raina, W. Leslie, 2018, BMC Geriatrics.

Calcium and vitamin D intake and mortality: results from the Canadian Multicentre Osteoporosis Study (CaMos).

Jacques P. Brown, S. Jamal, W. Leslie, 2013, The Journal of clinical endocrinology and metabolism.

Jacques P. Brown, S. Jamal, W. Zhou, 2009, Canadian journal of public health = Revue canadienne de sante publique.

Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency

S. Stockler-Ipsiroglu, Bojana Rakić, G. Hendson, 2019, Molecular genetics and metabolism reports.

Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiency

S. Stockler-Ipsiroglu, Bojana Rakić, G. Hendson, 2019, Molecular genetics and metabolism reports.

Genetic determinants of bone mass acquisition and risk for osteoporosis

Millan S Patel, L. Rubin, D. E. Cole, 2000 .

Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study

Phillip A. Richmond, W. Wasserman, C. Boerkoel, 2022, HGG advances.

Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications

C. Boerkoel, M. Demos, H. Gill, 2021, Cold Spring Harbor molecular case studies.

Pontocerebellar Hypoplasia: Review of Classification and Genetics, and Exclusion of Several Genes Known to Be Important for Cerebellar Development

H. Zoghbi, D. Chitayat, S. Maricich, 2011, Journal of child neurology.

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

Allen D. Delaney, M. Marra, A. Delaney, 2009, BMC Genomics.

The circadian modulation of leptin-controlled bone formation.

L. Fu, G. Karsenty, Millan S Patel, 2006, Progress in brain research.

Regulation of bone formation and vision by LRP5.

G. Karsenty, Millan S Patel, M. Patel, 2002, The New England journal of medicine.

Alternating hypoglycemia and hyperglycemia in a toddler with a homozygous p.R1419H ABCC8 mutation: an unusual clinical picture

S. Ellard, C. V. van Karnebeek, S. Flanagan, 2015, Journal of pediatric endocrinology & metabolism : JPEM.