Millan S. Patel - Concepedia

Author

Millan S. Patel

Also Known As

Cheryl Y. Gregory-Evans, Janez Prezelj, M Patel, M S Patel, M. Patel, M. S. Patel, M.S. Patel, Madison Patel, Millan Patel, Millan S Patel

103

Publications

7.2K

Citations

H-Index

Concepts

All Affiliations

University of British Columbia University of Toronto Child and Family Research Institute Baylor College of Medicine BC Children's Hospital

About

Millan S. Patel is an author at University of British Columbia specializing in medicine, genetics, and osteoporosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	17	4.5K
2	Public Health	3	3	135
3	Health Sciences	2	2	1.1K
4	Social Sciences	1	1	68
5	Biology	1	1	68

Millan S. Patel

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
Canonical Wnt Signaling in Differentiated Osteoblasts Controls Osteoclast Differentiation Donald A. Glass, Peter Bialek, Jong Deok Ahn, Developmental Cell Bone Morphogenic ProteinOsteoarthritisCanonical Wnt SignalingMedicineCell Biology	2005	1.5K
<i>Cbfa1</i>-independent decrease in osteoblast proliferation, osteopenia, and persistent embryonic eye vascularization in mice deficient in Lrp5, a Wnt coreceptor Masaki Kato, Millan S. Patel, Régis Levasseur, The Journal of Cell Biology Osteoblast ProliferationImmunologyCell DeathHuman Osteoporosis-pseudoglioma SyndromeCellular Physiology	2002	1.1K
The Molecular Clock Mediates Leptin-Regulated Bone Formation Loning Fu, Millan S. Patel, Allan Bradley, Cell SclerostinSignal TransductionMolecular PhysiologyCytoskeletonBone Homeostasis	2005	564
WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature Ivan B. Lobov, Sujata Rao, Thomas J. Carroll, Nature InflammationCytokineApoptosisImmunologyCell Death	2005	420
22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome Shay Ben‐Shachar, Zhishuo Ou, Chad A. Shaw, The American Journal of Human Genetics Distal DeletionDigeorge SyndromeGenetic DisorderGeneticsPathology	2008	244
Mutations in NOTCH1 Cause Adams-Oliver Syndrome Anna-Barbara Stittrich, Anna Lehman, Dale L. Bodian, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyGenetic DisorderGeneticsPathogenesis	2014	185
Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome Josephina Meester, Laura Southgate, Anna-Barbara Stittrich, The American Journal of Human Genetics Developmental AnomalyMendelian DisorderGenetic DisorderGeneticsPathogenesis	2015	89
RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit—successes and challenges Alison M. Elliott, Christèle du Souich, Anna Lehman, European Journal of Pediatrics SequencingNext-generation SequencingGeneticsNewborn MedicineGenome Sequencing	2019	84
Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams–Oliver syndrome Millan S. Patel, Glenn Taylor, Simi Bharya, American Journal of Medical Genetics Part A HypertensionVascular DiseaseBlood Vessel AbnormalitiesVascular MalformationPulmonary Alveolar Proteinosis	2004	72
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization Shelin Adam, Laura Arbour, Linlea Armstrong, BMC Genomics	2009	69

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