Publications by authors named "Millan S Patel"

35Publications

Pathologic Skull Fracture in a Near-Term Neonate with Arthrochalasia Type Ehlers-Danlos Syndrome: A Case Report.

Fetal Pediatr Pathol 2020 Apr 27:1-6. Epub 2020 Apr 27.

Department of Pathology and Laboratory Medicine, Children's and Women's Health Centre of British Columbia, and University of British Columbia, Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1080/15513815.2020.1753269DOI Listing
April 2020

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

Sci Rep 2017 06 13;7(1):3432. Epub 2017 Jun 13.

Centre for Menstrual Cycle and Ovulation Research, Division of Endocrinology, Department of Medicine, University of British Columbia; Vancouver Coastal Health Research Institute, Vancouver, Canada.

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http://www.nature.com/articles/s41598-017-03685-x
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http://dx.doi.org/10.1038/s41598-017-03685-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469792PMC
June 2017

Diagnosis of Van den Ende-Gupta syndrome: Approach to the Marden-Walker-like spectrum of disorders.

Am J Med Genet A 2016 09 4;170(9):2310-21. Epub 2016 Jul 4.

Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1002/ajmg.a.37831DOI Listing
September 2016

Mutations in NOTCH1 cause Adams-Oliver syndrome.

Am J Hum Genet 2014 Sep 14;95(3):275-84. Epub 2014 Aug 14.

Department of Medical Genetics and Child and Family Research Institute, University of British Columbia, Vancouver, BC V6H 3N1, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.07.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157158PMC
September 2014

Anterolateral diaphragmatic hernia with body wall defect understood in relation to the abaxial domain.

Am J Med Genet A 2014 Jul 3;164A(7):1860-2. Epub 2014 Apr 3.

Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.36529
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http://dx.doi.org/10.1002/ajmg.a.36529DOI Listing
July 2014

A cryptic familial rearrangement of 11p15.5, involving both imprinting centers, in a family with a history of short stature.

Am J Med Genet A 2014 Jun 25;164A(6):1587-94. Epub 2014 Mar 25.

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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http://dx.doi.org/10.1002/ajmg.a.36490DOI Listing
June 2014

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.

J Med Genet 2014 Feb 16;51(2):122-31. Epub 2013 Dec 16.

Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://www.molepi.nl/uploads/publicaties/2014/2014_oei_jmedg
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http://jmg.bmj.com/cgi/doi/10.1136/jmedgenet-2013-102064
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http://dx.doi.org/10.1136/jmedgenet-2013-102064DOI Listing
February 2014

Combined immunodeficiency associated with homozygous MALT1 mutations.

J Allergy Clin Immunol 2014 May 12;133(5):1458-62, 1462.e1-7. Epub 2013 Dec 12.

Department of Pediatrics, Child & Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2013.10.045DOI Listing
May 2014

Assessment of gene-by-sex interaction effect on bone mineral density.

J Bone Miner Res 2012 Oct;27(10):2051-64

Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue CT3, Boston,MA 02118, USA.

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http://dx.doi.org/10.1002/jbmr.1679DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447125PMC
October 2012

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

Authors:
Karol Estrada Unnur Styrkarsdottir Evangelos Evangelou Yi-Hsiang Hsu Emma L Duncan Evangelia E Ntzani Ling Oei Omar M E Albagha Najaf Amin John P Kemp Daniel L Koller Guo Li Ching-Ti Liu Ryan L Minster Alireza Moayyeri Liesbeth Vandenput Dana Willner Su-Mei Xiao Laura M Yerges-Armstrong Hou-Feng Zheng Nerea Alonso Joel Eriksson Candace M Kammerer Stephen K Kaptoge Paul J Leo Gudmar Thorleifsson Scott G Wilson James F Wilson Ville Aalto Markku Alen Aaron K Aragaki Thor Aspelund Jacqueline R Center Zoe Dailiana David J Duggan Melissa Garcia Natàlia Garcia-Giralt Sylvie Giroux Göran Hallmans Lynne J Hocking Lise Bjerre Husted Karen A Jameson Rita Khusainova Ghi Su Kim Charles Kooperberg Theodora Koromila Marcin Kruk Marika Laaksonen Andrea Z Lacroix Seung Hun Lee Ping C Leung Joshua R Lewis Laura Masi Simona Mencej-Bedrac Tuan V Nguyen Xavier Nogues Millan S Patel Janez Prezelj Lynda M Rose Serena Scollen Kristin Siggeirsdottir Albert V Smith Olle Svensson Stella Trompet Olivia Trummer Natasja M van Schoor Jean Woo Kun Zhu Susana Balcells Maria Luisa Brandi Brendan M Buckley Sulin Cheng Claus Christiansen Cyrus Cooper George Dedoussis Ian Ford Morten Frost David Goltzman Jesús González-Macías Mika Kähönen Magnus Karlsson Elza Khusnutdinova Jung-Min Koh Panagoula Kollia Bente Lomholt Langdahl William D Leslie Paul Lips Östen Ljunggren Roman S Lorenc Janja Marc Dan Mellström Barbara Obermayer-Pietsch José M Olmos Ulrika Pettersson-Kymmer David M Reid José A Riancho Paul M Ridker François Rousseau P Eline Slagboom Nelson L S Tang Roser Urreizti Wim Van Hul Jorma Viikari María T Zarrabeitia Yurii S Aulchenko Martha Castano-Betancourt Elin Grundberg Lizbeth Herrera Thorvaldur Ingvarsson Hrefna Johannsdottir Tony Kwan Rui Li Robert Luben Carolina Medina-Gómez Stefan Th Palsson Sjur Reppe Jerome I Rotter Gunnar Sigurdsson Joyce B J van Meurs Dominique Verlaan Frances M K Williams Andrew R Wood Yanhua Zhou Kaare M Gautvik Tomi Pastinen Soumya Raychaudhuri Jane A Cauley Daniel I Chasman Graeme R Clark Steven R Cummings Patrick Danoy Elaine M Dennison Richard Eastell John A Eisman Vilmundur Gudnason Albert Hofman Rebecca D Jackson Graeme Jones J Wouter Jukema Kay-Tee Khaw Terho Lehtimäki Yongmei Liu Mattias Lorentzon Eugene McCloskey Braxton D Mitchell Kannabiran Nandakumar Geoffrey C Nicholson Ben A Oostra Munro Peacock Huibert A P Pols Richard L Prince Olli Raitakari Ian R Reid John Robbins Philip N Sambrook Pak Chung Sham Alan R Shuldiner Frances A Tylavsky Cornelia M van Duijn Nick J Wareham L Adrienne Cupples Michael J Econs David M Evans Tamara B Harris Annie Wai Chee Kung Bruce M Psaty Jonathan Reeve Timothy D Spector Elizabeth A Streeten M Carola Zillikens Unnur Thorsteinsdottir Claes Ohlsson David Karasik J Brent Richards Matthew A Brown Kari Stefansson André G Uitterlinden Stuart H Ralston John P A Ioannidis Douglas P Kiel Fernando Rivadeneira

Nat Genet 2012 Apr 15;44(5):491-501. Epub 2012 Apr 15.

Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://kooperberg.fhcrc.org/papers/2012estrada.pdf
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http://www.nature.com/doifinder/10.1038/ng.2249
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http://dx.doi.org/10.1038/ng.2249DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338864PMC
April 2012

Childhood-onset hemiatrophy caused by unilateral morphea.

Clin Dysmorphol 2009 Oct;18(4):213-4

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

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https://insights.ovid.com/crossref?an=00019605-200910000-000
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http://dx.doi.org/10.1097/MCD.0b013e32832a9e0cDOI Listing
October 2009

Sudden death in spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type.

Clin Dysmorphol 2009 Jan;18(1):25-9

Centro de Genética Médica Doutor Jacinto Magalhães, Porto, Portugal.

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http://dx.doi.org/10.1097/MCD.0b013e3283186907DOI Listing
January 2009

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.

Am J Med Genet A 2008 May;146A(10):1299-306

Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.32277
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http://dx.doi.org/10.1002/ajmg.a.32277DOI Listing
May 2008

Preaxial polydactyly in neurofibromatosis 1.

Clin Dysmorphol 2007 Jul;16(3):193-4

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

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http://dx.doi.org/10.1097/MCD.0b013e3280e1cc54DOI Listing
July 2007

The circadian modulation of leptin-controlled bone formation.

Prog Brain Res 2006 ;153:177-88

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

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http://dx.doi.org/10.1016/S0079-6123(06)53010-9DOI Listing
November 2006

Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5?

Am J Med Genet A 2006 Mar;140(6):594-603

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.

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http://dx.doi.org/10.1002/ajmg.a.31095DOI Listing
March 2006

WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature.

Nature 2005 Sep;437(7057):417-21

Division of Developmental Biology, The Children's Hospital Research Foundation and Department of Ophthalmology, University of Cincinnati, Cincinnati, Ohio 45229, USA.

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http://dx.doi.org/10.1038/nature03928DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259146PMC
September 2005

The molecular clock mediates leptin-regulated bone formation.

Cell 2005 Sep;122(5):803-15

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; Bone Disease Program of Texas, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1016/j.cell.2005.06.028DOI Listing
September 2005

Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams-Oliver syndrome.

Am J Med Genet A 2004 Sep;129A(3):294-9

Department of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.30221DOI Listing
September 2004

A new insight into the formation of osteolytic lesions in multiple myeloma.

N Engl J Med 2003 Dec;349(26):2479-80

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, USA.

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http://www.nejm.org/doi/abs/10.1056/NEJMp038176
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http://dx.doi.org/10.1056/NEJMp038176DOI Listing
December 2003

Regulation of bone formation and vision by LRP5.

N Engl J Med 2002 May;346(20):1572-4

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http://dx.doi.org/10.1056/NEJM200205163462011DOI Listing
May 2002