Eric K Moses

Eric K Moses

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Eric K Moses

Eric K Moses

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Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes.

J Hypertens 2019 May;37(5):997-1011

The Curtin/UWA Centre for Genetic Origins of Health and Disease, School of Pharmacy and Biomedical Sciences, Faculty of Health Sciences, Curtin University.

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http://dx.doi.org/10.1097/HJH.0000000000002023DOI Listing
May 2019

Identification of novel sarcoma risk genes using a two-stage genome wide DNA sequencing strategy in cancer cluster families and population case and control cohorts.

BMC Med Genet 2019 May 3;20(1):69. Epub 2019 May 3.

The Curtin UWA Centre for Genetic Origins of Health and Disease, Faculty of Health Sciences, Curtin University and Faculty of Health and Medical Sciences, M409 The University of Western Australia, 35 Stirling Hwy, Crawley, 6009, Western Australia.

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https://bmcmedgenet.biomedcentral.com/articles/10.1186/s1288
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http://dx.doi.org/10.1186/s12881-019-0808-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499942PMC
May 2019

To test, or not to test: that is the question for the future of lipoprotein(a).

Expert Rev Cardiovasc Ther 2019 Apr 3;17(4):241-250. Epub 2019 Apr 3.

b School of Medicine, Faculty of Medicine and Health Sciences , University of Western Australia , Perth , Australia.

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http://dx.doi.org/10.1080/14779072.2019.1596799DOI Listing
April 2019

Analysis of the Epigenome in Multiplex Pre-eclampsia Families Identifies , , and as Novel Candidate Risk Genes.

Front Genet 2019 19;10:227. Epub 2019 Mar 19.

The Curtin UWA Centre for Genetic Origins of Health and Disease, Faculty of Health and Medical Sciences, Curtin University, The University of Western Australia, Perth, WA, Australia.

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http://dx.doi.org/10.3389/fgene.2019.00227DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434177PMC
March 2019

Genetic Approaches in Preeclampsia.

Methods Mol Biol 2018 ;1710:53-72

Centre for Genetic Origins of Health and Disease, The University of Western Australia, Perth, Australia.

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http://link.springer.com/10.1007/978-1-4939-7498-6_5
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http://dx.doi.org/10.1007/978-1-4939-7498-6_5DOI Listing
July 2018

Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity.

Schizophr Res 2018 Jul 24;197:337-345. Epub 2018 Feb 24.

Centre for Clinical Research in Neuropsychiatry, School of Psychiatry and Clinical Neurosciences, University of Western Australia, MRF Building, 50 Murray Street, Perth 6000, Australia; Cooperative Research Centre for Mental Health, Carlton, South Victoria, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.schres.2018.02.034DOI Listing
July 2018

Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study.

Hum Genet 2018 Jan 27;137(1):45-53. Epub 2017 Nov 27.

Centre for Genetic Origins of Health and Disease, Faculty of Health and Medical Sciences, The University of Western Australia, Perth, Australia.

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http://dx.doi.org/10.1007/s00439-017-1856-xDOI Listing
January 2018

Exome array analysis suggests an increased variant burden in families with schizophrenia.

Schizophr Res 2017 07 9;185:9-16. Epub 2016 Dec 9.

Centre for Clinical Research in Neuropsychiatry, School of Psychiatry and Clinical Neurosciences, University of Western Australia, MRF Building, 50 Murray Street, Perth 6000, Australia; Cooperative Research Centre for Mental Health, Carlton, South, Victoria, Australia.

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http://dx.doi.org/10.1016/j.schres.2016.12.007DOI Listing
July 2017

ADAM19: A Novel Target for Metabolic Syndrome in Humans and Mice.

Mediators Inflamm 2017 7;2017:7281986. Epub 2017 Feb 7.

School of Medicine and Pharmacology, University of Western Australia, Crawley, Western Australia, Australia.

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http://dx.doi.org/10.1155/2017/7281986DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318628PMC
July 2017

Environment Changes Genetic Effects on Respiratory Conditions and Allergic Phenotypes.

Sci Rep 2017 07 24;7(1):6342. Epub 2017 Jul 24.

School of Public Health, Curtin University, Kent St, Bentley, 6102, Western Australia, Australia.

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http://dx.doi.org/10.1038/s41598-017-06791-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524954PMC
July 2017

The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia.

J Hypertens 2017 01;35(1):132-139

aDepartment of Gynecology and Obstetrics, Haukeland University Hospital bDepartment of Clinical Science, University of Bergen, Bergen, Norway cCentre for Genetic Origins of Health and Disease, University of Western Australia, Perth, Australia dDepartment of Cancer Research and Molecular Medicine, Centre of Molecular Inflammation Research, Norwegian University of Science and Technology, Trondheim eDepartment of Heart Disease, Haukeland University Hospital, Bergen, Norway fSouth Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, Texas, USA gDepartment of Obstetrics and Gynaecology, University of Melbourne, Parkville hPregnancy Research Centre, Department of Maternal-Fetal Medicine, Royal Women's Hospital, Parkville, Victoria iFaculty of Health Sciences, Curtin University, Perth, Western Australia, Australia.

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http://dx.doi.org/10.1097/HJH.0000000000001131DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131692PMC
January 2017

Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes.

PLoS One 2015 26;10(5):e0128230. Epub 2015 May 26.

Centre for Genetic Origins of Health and Disease, The University of Western Australia, 35 Stirling Highway, Crawley, 6009, Western Australia, Australia.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0128230PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444079PMC
April 2016

Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort.

J Hypertens 2015 Nov;33(11):2294-302

aDepartment of Gynecology and Obstetrics, Haukeland University Hospital bDepartment of Clinical Science, University of Bergen, Bergen, Norway cCentre for Genetic Origins of Health and Disease, University of Western Australia, Perth, Australia dCentre of Molecular Inflammation Research, Norwegian University of Science and Technology, Trondheim eDepartment of Obstetrics and Gynecology, Stavanger University Hospital, Stavanger fDepartment of Cancer Research and Molecular Medicine gDepartment of Laboratory Medicine, Children's and Women's Health, Norwegian University of Science and Technology, Trondheim hDepartment of Heart Disease, Haukeland University Hospital, Bergen, Norway.

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https://insights.ovid.com/crossref?an=00004872-201511000-000
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http://dx.doi.org/10.1097/HJH.0000000000000696DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596487PMC
November 2015

The transcriptional landscape of age in human peripheral blood.

Authors:
Marjolein J Peters Roby Joehanes Luke C Pilling Claudia Schurmann Karen N Conneely Joseph Powell Eva Reinmaa George L Sutphin Alexandra Zhernakova Katharina Schramm Yana A Wilson Sayuko Kobes Taru Tukiainen Yolande F Ramos Harald H H Göring Myriam Fornage Yongmei Liu Sina A Gharib Barbara E Stranger Philip L De Jager Abraham Aviv Daniel Levy Joanne M Murabito Peter J Munson Tianxiao Huan Albert Hofman André G Uitterlinden Fernando Rivadeneira Jeroen van Rooij Lisette Stolk Linda Broer Michael M P J Verbiest Mila Jhamai Pascal Arp Andres Metspalu Liina Tserel Lili Milani Nilesh J Samani Pärt Peterson Silva Kasela Veryan Codd Annette Peters Cavin K Ward-Caviness Christian Herder Melanie Waldenberger Michael Roden Paula Singmann Sonja Zeilinger Thomas Illig Georg Homuth Hans-Jörgen Grabe Henry Völzke Leif Steil Thomas Kocher Anna Murray David Melzer Hanieh Yaghootkar Stefania Bandinelli Eric K Moses Jack W Kent Joanne E Curran Matthew P Johnson Sarah Williams-Blangero Harm-Jan Westra Allan F McRae Jennifer A Smith Sharon L R Kardia Iiris Hovatta Markus Perola Samuli Ripatti Veikko Salomaa Anjali K Henders Nicholas G Martin Alicia K Smith Divya Mehta Elisabeth B Binder K Maria Nylocks Elizabeth M Kennedy Torsten Klengel Jingzhong Ding Astrid M Suchy-Dicey Daniel A Enquobahrie Jennifer Brody Jerome I Rotter Yii-Der I Chen Jeanine Houwing-Duistermaat Margreet Kloppenburg P Eline Slagboom Quinta Helmer Wouter den Hollander Shannon Bean Towfique Raj Noman Bakhshi Qiao Ping Wang Lisa J Oyston Bruce M Psaty Russell P Tracy Grant W Montgomery Stephen T Turner John Blangero Ingrid Meulenbelt Kerry J Ressler Jian Yang Lude Franke Johannes Kettunen Peter M Visscher G Gregory Neely Ron Korstanje Robert L Hanson Holger Prokisch Luigi Ferrucci Tonu Esko Alexander Teumer Joyce B J van Meurs Andrew D Johnson

Nat Commun 2015 Oct 22;6:8570. Epub 2015 Oct 22.

The National Heart, Lung, and Blood Institute's and Boston University's Framingham Heart Study, Framingham, Massachusetts 01702, USA.

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http://dx.doi.org/10.1038/ncomms9570DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639797PMC
October 2015

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.

Nat Genet 2015 Sep 3;47(9):987-995. Epub 2015 Aug 3.

Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.

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http://dx.doi.org/10.1038/ng.3373DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557485PMC
September 2015

Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma.

Gene 2015 May 18;563(1):103-5. Epub 2015 Mar 18.

National Centre for Asbestos Related Disease, School of Medicine and Pharmacology, University of Western Australia, Nedlands, Western Australia 6009, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2015.03.031DOI Listing
May 2015

MACROD2 gene associated with autistic-like traits in a general population sample.

Psychiatr Genet 2014 Dec;24(6):241-248

Centre for Genetic Origins of Health and Disease, Telethon Institute for Child Health Research, University of Western Australia, Perth, Australia.

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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
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http://dx.doi.org/10.1097/YPG.0000000000000052DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320645PMC
December 2014

Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns.

BMC Genomics 2014 Nov 18;15:981. Epub 2014 Nov 18.

Centre for the Genetic Origins of Health and Disease (GOHaD), University of Western Australia, Perth, Australia.

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http://dx.doi.org/10.1186/1471-2164-15-981DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255932PMC
November 2014

The effect on melanoma risk of genes previously associated with telomere length.

J Natl Cancer Inst 2014 Oct 17;106(10). Epub 2014 Sep 17.

Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, Leeds Cancer Research UK Centre, University of Leeds, Leeds, UK (MMI, DTB, JCT, MHa, JRM, JANB, JHB); Oncogenomics (NKH), Genetic Epidemiology (NGM), Inflammatory Bowel Diseases Laboratory (GLRS), Cancer Control Group (DCW), Statistical Genetics (SM, MHL), and Molecular Epidemiology (GWM), QIMR Berghofer Medical Research Institute, Brisbane, Australia; INSERM, UMR-946, Genetic Variation and Human Diseases Unit, Paris, France (MB, FD); Université Paris Diderot, Sorbonne Paris Cité, Institut Universitaire d'Hématologie, Paris, France (MB, FD); Cancer Epidemiology and Services Research, Sydney School of Public Health, University of Sydney, Australia (AEC); Department of Oncology, University of Cambridge, Cambridge, UK (AMD, PDPP); Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX (JEL); Centre for Genetic Origins of Health and Disease, Faculty of Medicine, Dentistry and Health Sciences, University of Western Australia, Crawley, Australia (EKM, SVW); Centre for Cancer Biomarkers CCBIO (LAA) and Gade Laboratory for Pathology (AM), Department of Clinical Medicine, University of Bergen, Bergen, Norway; Department of Pathology, Haukeland University Hospital, Bergen, Norway (LAA); Department of Pathology, Molecular Pathology (PAA) and Department of Dermatology (PH), Oslo University Hospital, Rikshospitalet, Oslo, Norway; Assistance Publique-Hôpitaux de Paris, Hôpital Cochin, Service de Dermatologie, Université Paris Descartes, Paris, France (MFA); Department of Dermatology (EA) and Oncogenics Unit (EA, EF), Sheba Medical Center, Tel Hashomer, Sackler Faculty of Medicine, Tel Aviv, Israel (EA); Department of Internal Medicine and Medical Specialties, University of Genoa, Genoa, Italy (GBS, EFPG); Laboratory of Genetics of Rare Hereditary Cancers, San Martino-IST Research Hospital, Genoa, Italy (GBS, EFPG); Division of Cancer Epidemiology and Gene

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https://genepi.qimr.edu.au/contents/p/staff/IlesMM_JNCI_EPUB
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http://jnci.oxfordjournals.org/cgi/doi/10.1093/jnci/dju267
Publisher Site
http://dx.doi.org/10.1093/jnci/dju267DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196080PMC
October 2014

Plasma levels of soluble interleukin 1 receptor accessory protein are reduced in obesity.

J Clin Endocrinol Metab 2014 Sep 10;99(9):3435-43. Epub 2014 Jun 10.

Baker IDI Heart and Diabetes Institute (K.B., C.A., N.C., K.A.S., P.Z., J.B.M.J.), Melbourne, Victoria 3004, Australia; Texas Biomedical Research Institute (H.K., V.P.D., M.A.C., M.P.J., T.D.D., A.G.C., L.A., E.K.M., H.H.H.G., J.E.C., J.B.), San Antonio, Texas 78245-0549; and Ministry of Health and Quality of Life (S.K.), Port Louis, Mauritius.

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http://dx.doi.org/10.1210/jc.2013-4475DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154095PMC
September 2014

Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens.

Genet Epidemiol 2014 Jul;38(5):439-46

Departent of Genetics, Texas Biomedical Research Institute, San Antonio, Texas, United States of America; Division of Public Health Sciences, Fred Hutchinson Cancer Research Institute, Seattle, Washington, United States of America.

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http://dx.doi.org/10.1002/gepi.21817DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171053PMC
July 2014

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.

Authors:
Paul M Thompson Jason L Stein Sarah E Medland Derrek P Hibar Alejandro Arias Vasquez Miguel E Renteria Roberto Toro Neda Jahanshad Gunter Schumann Barbara Franke Margaret J Wright Nicholas G Martin Ingrid Agartz Martin Alda Saud Alhusaini Laura Almasy Jorge Almeida Kathryn Alpert Nancy C Andreasen Ole A Andreassen Liana G Apostolova Katja Appel Nicola J Armstrong Benjamin Aribisala Mark E Bastin Michael Bauer Carrie E Bearden Orjan Bergmann Elisabeth B Binder John Blangero Henry J Bockholt Erlend Bøen Catherine Bois Dorret I Boomsma Tom Booth Ian J Bowman Janita Bralten Rachel M Brouwer Han G Brunner David G Brohawn Randy L Buckner Jan Buitelaar Kazima Bulayeva Juan R Bustillo Vince D Calhoun Dara M Cannon Rita M Cantor Melanie A Carless Xavier Caseras Gianpiero L Cavalleri M Mallar Chakravarty Kiki D Chang Christopher R K Ching Andrea Christoforou Sven Cichon Vincent P Clark Patricia Conrod Giovanni Coppola Benedicto Crespo-Facorro Joanne E Curran Michael Czisch Ian J Deary Eco J C de Geus Anouk den Braber Giuseppe Delvecchio Chantal Depondt Lieuwe de Haan Greig I de Zubicaray Danai Dima Rali Dimitrova Srdjan Djurovic Hongwei Dong Gary Donohoe Ravindranath Duggirala Thomas D Dyer Stefan Ehrlich Carl Johan Ekman Torbjørn Elvsåshagen Louise Emsell Susanne Erk Thomas Espeseth Jesen Fagerness Scott Fears Iryna Fedko Guillén Fernández Simon E Fisher Tatiana Foroud Peter T Fox Clyde Francks Sophia Frangou Eva Maria Frey Thomas Frodl Vincent Frouin Hugh Garavan Sudheer Giddaluru David C Glahn Beata Godlewska Rita Z Goldstein Randy L Gollub Hans J Grabe Oliver Grimm Oliver Gruber Tulio Guadalupe Raquel E Gur Ruben C Gur Harald H H Göring Saskia Hagenaars Tomas Hajek Geoffrey B Hall Jeremy Hall John Hardy Catharina A Hartman Johanna Hass Sean N Hatton Unn K Haukvik Katrin Hegenscheid Andreas Heinz Ian B Hickie Beng-Choon Ho David Hoehn Pieter J Hoekstra Marisa Hollinshead Avram J Holmes Georg Homuth Martine Hoogman L Elliot Hong Norbert Hosten Jouke-Jan Hottenga Hilleke E Hulshoff Pol Kristy S Hwang Clifford R Jack Mark Jenkinson Caroline Johnston Erik G Jönsson René S Kahn Dalia Kasperaviciute Sinead Kelly Sungeun Kim Peter Kochunov Laura Koenders Bernd Krämer John B J Kwok Jim Lagopoulos Gonzalo Laje Mikael Landen Bennett A Landman John Lauriello Stephen M Lawrie Phil H Lee Stephanie Le Hellard Herve Lemaître Cassandra D Leonardo Chiang-Shan Li Benny Liberg David C Liewald Xinmin Liu Lorna M Lopez Eva Loth Anbarasu Lourdusamy Michelle Luciano Fabio Macciardi Marise W J Machielsen Glenda M Macqueen Ulrik F Malt René Mandl Dara S Manoach Jean-Luc Martinot Mar Matarin Karen A Mather Manuel Mattheisen Morten Mattingsdal Andreas Meyer-Lindenberg Colm McDonald Andrew M McIntosh Francis J McMahon Katie L McMahon Eva Meisenzahl Ingrid Melle Yuri Milaneschi Sebastian Mohnke Grant W Montgomery Derek W Morris Eric K Moses Bryon A Mueller Susana Muñoz Maniega Thomas W Mühleisen Bertram Müller-Myhsok Benson Mwangi Matthias Nauck Kwangsik Nho Thomas E Nichols Lars-Göran Nilsson Allison C Nugent Lars Nyberg Rene L Olvera Jaap Oosterlaan Roel A Ophoff Massimo Pandolfo Melina Papalampropoulou-Tsiridou Martina Papmeyer Tomas Paus Zdenka Pausova Godfrey D Pearlson Brenda W Penninx Charles P Peterson Andrea Pfennig Mary Phillips G Bruce Pike Jean-Baptiste Poline Steven G Potkin Benno Pütz Adaikalavan Ramasamy Jerod Rasmussen Marcella Rietschel Mark Rijpkema Shannon L Risacher Joshua L Roffman Roberto Roiz-Santiañez Nina Romanczuk-Seiferth Emma J Rose Natalie A Royle Dan Rujescu Mina Ryten Perminder S Sachdev Alireza Salami Theodore D Satterthwaite Jonathan Savitz Andrew J Saykin Cathy Scanlon Lianne Schmaal Hugo G Schnack Andrew J Schork S Charles Schulz Remmelt Schür Larry Seidman Li Shen Jody M Shoemaker Andrew Simmons Sanjay M Sisodiya Colin Smith Jordan W Smoller Jair C Soares Scott R Sponheim Emma Sprooten John M Starr Vidar M Steen Stephen Strakowski Lachlan Strike Jessika Sussmann Philipp G Sämann Alexander Teumer Arthur W Toga Diana Tordesillas-Gutierrez Daniah Trabzuni Sarah Trost Jessica Turner Martijn Van den Heuvel Nic J van der Wee Kristel van Eijk Theo G M van Erp Neeltje E M van Haren Dennis van 't Ent Marie-Jose van Tol Maria C Valdés Hernández Dick J Veltman Amelia Versace Henry Völzke Robert Walker Henrik Walter Lei Wang Joanna M Wardlaw Michael E Weale Michael W Weiner Wei Wen Lars T Westlye Heather C Whalley Christopher D Whelan Tonya White Anderson M Winkler Katharina Wittfeld Girma Woldehawariat Christiane Wolf David Zilles Marcel P Zwiers Anbupalam Thalamuthu Peter R Schofield Nelson B Freimer Natalia S Lawrence Wayne Drevets

Brain Imaging Behav 2014 Jun;8(2):153-82

Imaging Genetics Center, Institute for Neuroimaging and Informatics, Keck School of Medicine, University of Southern California, 2001 N. Soto Street, Los Angeles, CA, 90033, USA,

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http://dx.doi.org/10.1007/s11682-013-9269-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008818PMC
June 2014

Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1.

Eur J Hum Genet 2014 May 18;22(5):688-95. Epub 2013 Sep 18.

1] School of Chemistry and Biochemistry, University of Western Australia, Crawley, WA, Australia [2] Centre for Genetic Origins of Health and Disease (GOHaD), University of Western Australia, Crawley, WA, Australia.

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http://www.nature.com/articles/ejhg2013208
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http://dx.doi.org/10.1038/ejhg.2013.208DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992570PMC
May 2014

Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22.

Pregnancy Hypertens 2014 Apr 22;4(2):178-85. Epub 2014 Mar 22.

Centre for Genetic Origins of Health and Disease, The University of Western Australia, Perth, WA 6009, Australia.

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http://dx.doi.org/10.1016/j.preghy.2014.03.005DOI Listing
April 2014

A genome-wide association study for malignant mesothelioma risk.

Lung Cancer 2013 Oct 1;82(1):1-8. Epub 2013 Jul 1.

Centre for Genetic Origins of Health and Disease, University of Western Australia, 35 Stirling Hwy, Crawley, Western Australia 6009, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.lungcan.2013.04.018DOI Listing
October 2013

Genome-wide association study of autistic-like traits in a general population study of young adults.

Front Hum Neurosci 2013 11;7:658. Epub 2013 Oct 11.

Centre for Genetic Origins of Health and Disease, University of Western Australia , Perth, WA , Australia.

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http://dx.doi.org/10.3389/fnhum.2013.00658DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795398PMC
October 2013

Identification of common variants associated with human hippocampal and intracranial volumes.

Authors:
Jason L Stein Sarah E Medland Alejandro Arias Vasquez Derrek P Hibar Rudy E Senstad Anderson M Winkler Roberto Toro Katja Appel Richard Bartecek Ørjan Bergmann Manon Bernard Andrew A Brown Dara M Cannon M Mallar Chakravarty Andrea Christoforou Martin Domin Oliver Grimm Marisa Hollinshead Avram J Holmes Georg Homuth Jouke-Jan Hottenga Camilla Langan Lorna M Lopez Narelle K Hansell Kristy S Hwang Sungeun Kim Gonzalo Laje Phil H Lee Xinmin Liu Eva Loth Anbarasu Lourdusamy Morten Mattingsdal Sebastian Mohnke Susana Muñoz Maniega Kwangsik Nho Allison C Nugent Carol O'Brien Martina Papmeyer Benno Pütz Adaikalavan Ramasamy Jerod Rasmussen Mark Rijpkema Shannon L Risacher J Cooper Roddey Emma J Rose Mina Ryten Li Shen Emma Sprooten Eric Strengman Alexander Teumer Daniah Trabzuni Jessica Turner Kristel van Eijk Theo G M van Erp Marie-Jose van Tol Katharina Wittfeld Christiane Wolf Saskia Woudstra Andre Aleman Saud Alhusaini Laura Almasy Elisabeth B Binder David G Brohawn Rita M Cantor Melanie A Carless Aiden Corvin Michael Czisch Joanne E Curran Gail Davies Marcio A A de Almeida Norman Delanty Chantal Depondt Ravi Duggirala Thomas D Dyer Susanne Erk Jesen Fagerness Peter T Fox Nelson B Freimer Michael Gill Harald H H Göring Donald J Hagler David Hoehn Florian Holsboer Martine Hoogman Norbert Hosten Neda Jahanshad Matthew P Johnson Dalia Kasperaviciute Jack W Kent Peter Kochunov Jack L Lancaster Stephen M Lawrie David C Liewald René Mandl Mar Matarin Manuel Mattheisen Eva Meisenzahl Ingrid Melle Eric K Moses Thomas W Mühleisen Matthias Nauck Markus M Nöthen Rene L Olvera Massimo Pandolfo G Bruce Pike Ralf Puls Ivar Reinvang Miguel E Rentería Marcella Rietschel Joshua L Roffman Natalie A Royle Dan Rujescu Jonathan Savitz Hugo G Schnack Knut Schnell Nina Seiferth Colin Smith Vidar M Steen Maria C Valdés Hernández Martijn Van den Heuvel Nic J van der Wee Neeltje E M Van Haren Joris A Veltman Henry Völzke Robert Walker Lars T Westlye Christopher D Whelan Ingrid Agartz Dorret I Boomsma Gianpiero L Cavalleri Anders M Dale Srdjan Djurovic Wayne C Drevets Peter Hagoort Jeremy Hall Andreas Heinz Clifford R Jack Tatiana M Foroud Stephanie Le Hellard Fabio Macciardi Grant W Montgomery Jean Baptiste Poline David J Porteous Sanjay M Sisodiya John M Starr Jessika Sussmann Arthur W Toga Dick J Veltman Henrik Walter Michael W Weiner Joshua C Bis M Arfan Ikram Albert V Smith Vilmundur Gudnason Christophe Tzourio Meike W Vernooij Lenore J Launer Charles DeCarli Sudha Seshadri Ole A Andreassen Liana G Apostolova Mark E Bastin John Blangero Han G Brunner Randy L Buckner Sven Cichon Giovanni Coppola Greig I de Zubicaray Ian J Deary Gary Donohoe Eco J C de Geus Thomas Espeseth Guillén Fernández David C Glahn Hans J Grabe John Hardy Hilleke E Hulshoff Pol Mark Jenkinson René S Kahn Colm McDonald Andrew M McIntosh Francis J McMahon Katie L McMahon Andreas Meyer-Lindenberg Derek W Morris Bertram Müller-Myhsok Thomas E Nichols Roel A Ophoff Tomas Paus Zdenka Pausova Brenda W Penninx Steven G Potkin Philipp G Sämann Andrew J Saykin Gunter Schumann Jordan W Smoller Joanna M Wardlaw Michael E Weale Nicholas G Martin Barbara Franke Margaret J Wright Paul M Thompson

Nat Genet 2012 Apr 15;44(5):552-61. Epub 2012 Apr 15.

Laboratory of Neuro Imaging, David Geffen School of Medicine, University of California, Los Angeles, California, USA.

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http://dx.doi.org/10.1038/ng.2250DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635491PMC
April 2012

Inherited thrombophilias and adverse pregnancy outcomes: a case-control study in an Australian population.

Acta Obstet Gynecol Scand 2012 Feb 9;91(2):250-5. Epub 2011 Nov 9.

Department of Perinatal Medicine, The Royal Women's Hospital, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1111/j.1600-0412.2011.01293.xDOI Listing
February 2012

Diverse biological activities of the vascular non-inflammatory molecules - the Vanin pantetheinases.

Biochem Biophys Res Commun 2012 Jan 1;417(2):653-8. Epub 2011 Dec 1.

School of Biomedical, Biomolecular and Chemical Sciences, University of Western Australia, Crawley, WA 6009, Australia.

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http://linkinghub.elsevier.com/retrieve/pii/S0006291X1102120
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http://dx.doi.org/10.1016/j.bbrc.2011.11.099DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259148PMC
January 2012

The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells.

J Med Genet 2011 Aug 5;48(8):563-6. Epub 2011 May 5.

Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX 78245-0549, USA.

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http://dx.doi.org/10.1136/jmg.2010.083303DOI Listing
August 2011

Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model.

Hum Genet 2011 Jan 8;129(1):25-34. Epub 2010 Oct 8.

Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Kvinne-barn senteret, 1.etg. Øst, 7006 Trondheim, Norway.

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http://dx.doi.org/10.1007/s00439-010-0893-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332147PMC
January 2011

A transcriptional profile of the decidua in preeclampsia.

Am J Obstet Gynecol 2011 Jan;204(1):84.e1-27

Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

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http://dx.doi.org/10.1016/j.ajog.2010.08.043DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011026PMC
January 2011

Molecular markers of preterm labor in the choriodecidua.

Reprod Sci 2010 Mar 15;17(3):297-310. Epub 2009 Dec 15.

Department of Obstetrics & Gynaecology, The University of Melbourne, Australia.

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http://dx.doi.org/10.1177/1933719109353454DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2852874PMC
March 2010

Genetic variation at the FTO locus influences RBL2 gene expression.

Diabetes 2010 Mar 15;59(3):726-32. Epub 2009 Dec 15.

Department of Genomics and Systems Biology, Baker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.2337/db09-1277DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828652PMC
March 2010

The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations.

Hum Genet 2009 Nov 4;126(5):655-66. Epub 2009 Jul 4.

Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, TX 78227, USA.

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http://dx.doi.org/10.1007/s00439-009-0714-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783187PMC
November 2009

Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study).

Eur J Hum Genet 2009 Feb 10;17(2):250-7. Epub 2008 Sep 10.

Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.

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http://dx.doi.org/10.1038/ejhg.2008.158DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696227PMC
February 2009

The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population.

Aust N Z J Obstet Gynaecol 2008 Dec;48(6):536-41

Department of Obstetrics and Gynaecology, The University of Melbourne, The Royal Women's Hospital, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1111/j.1479-828X.2008.00919.xDOI Listing
December 2008

Genetic association of preeclampsia to the inflammatory response gene SEPS1.

Am J Obstet Gynecol 2008 Mar 20;198(3):336.e1-5. Epub 2008 Feb 20.

Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, TX 78245-0549, USA.

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http://dx.doi.org/10.1016/j.ajog.2007.09.024DOI Listing
March 2008

Genetic determinants of mitochondrial content.

Hum Mol Genet 2007 Jun 27;16(12):1504-14. Epub 2007 Apr 27.

Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, TX 78227, USA.

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http://dx.doi.org/10.1093/hmg/ddm101DOI Listing
June 2007

The -56T HLA-G promoter polymorphism is not associated with pre-eclampsia/eclampsia in Australian and New Zealand women.

Hypertens Pregnancy 2006 ;25(2):63-71

Department of Perinatal Medicine, The Royal Women's Hospital, Carlton, Victoria, Australia.

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http://www.tandfonline.com/doi/full/10.1080/1064195050054378
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http://dx.doi.org/10.1080/10641950500543780DOI Listing
September 2006

5 Beta-dihydroprogesterone and steroid 5 beta-reductase decrease in association with human parturition at term.

Mol Hum Reprod 2005 Jul;11(7):495-501

Pregnancy Research Centre and University of Melbourne Department of Obstetrics and Gynaecology, Royal Women's Hospital, Carlton, Victoria, Australia.

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http://academic.oup.com/molehr/article/11/7/495/982788/5βDi
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http://dx.doi.org/10.1093/molehr/gah201DOI Listing
July 2005

An emerging role for comprehensive proteome analysis in human pregnancy research.

Reproduction 2005 Jun;129(6):685-96

Department of Obstetrics and Gynaecology, The University of Melbourne, Melbourne, Australia.

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http://dx.doi.org/10.1530/rep.1.00524DOI Listing
June 2005

Association of the TNF2 allele with eclampsia.

Gynecol Obstet Invest 2004 9;57(4):204-9. Epub 2004 Feb 9.

Department of Perinatal Medicine and University of Melbourne Department of Obstetrics and Gynaecology, Royal Women's Hospital, Carlton, Victoria, Australia.

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http://dx.doi.org/10.1159/000076689DOI Listing
August 2004

Proteomic approaches in endometriosis research.

Proteomics 2004 Jul;4(7):1897-902

Departments of Perinatal Medicine and Gynaecology, The Royal Women's Hospital, 132 Grattan Street, Carlton, Melbourne 3053, Australia.

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http://dx.doi.org/10.1002/pmic.200300791DOI Listing
July 2004

Recombinant human zona pellucida proteins ZP1, ZP2 and ZP3 co-expressed in a human cell line.

Asian J Androl 2004 Mar;6(1):3-13

Department of Obstetrics and Gynaecology, University of Melbourne, 320 Victoria Parade, East Melbourne 3002 VIC, Australia.

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March 2004

Thrombomodulin Ala455Val dimorphism is not associated with pre-eclampsia in Australian and New Zealand women.

Gynecol Obstet Invest 2002 ;54(1):43-5

Department of Perinatal Medicine, The Royal Women's Hospital, Carlton, Vic., Australia.

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http://dx.doi.org/10.1159/000064696DOI Listing
December 2002