Publications Authored by Michael E Reschen

A retrospective analysis of outcomes in low- and intermediate-high-risk pulmonary embolism patients managed on an ambulatory medical unit in the UK.

Authors:

Michael E Reschen Jonathan Raby Jordan Bowen Sudhir Singh Daniel Lasserson Christopher A O'Callaghan

ERJ Open Res 2019 Apr 8;5(2). Epub 2019 Apr 8.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

Download full-text PDF	Source
http://openres.ersjournals.com/lookup/doi/10.1183/23120541.0	Publisher Site
http://dx.doi.org/10.1183/23120541.00184-2018	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452043	PMC

April 2019

A retrospective analysis of the utility and safety of kidney transplant biopsies by nephrology trainees and consultants.

Authors:

Michael E Reschen Andrea Mazzella Edward Sharples

Ann Med Surg (Lond) 2018 Apr 9;28:6-10. Epub 2018 Feb 9.

Oxford Kidney Unit, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Old Road, Oxford, OX3 7LE, United Kingdom.

View Article

Download full-text PDF	Source
http://dx.doi.org/10.1016/j.amsu.2018.02.001	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852268	PMC

April 2018

Outcomes of Elderly Patients with Anti-Neutrophil Cytoplasmic Autoantibody-Associated Vasculitis Treated with Immunosuppressive Therapy.

Authors:

Parminder K Judge Michael E Reschen Richard Haynes Edward J Sharples

Nephron 2016 20;133(4):223-31. Epub 2016 Jul 20.

Oxford Kidney Unit, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

View Article

Download full-text PDF	Source
http://dx.doi.org/10.1159/000447018	DOI Listing

February 2017

Genetic and environmental risk factors for atherosclerosis regulate transcription of phosphatase and actin regulating gene PHACTR1.

Authors:

Michael E Reschen Da Lin Anil Chalisey Elizabeth J Soilleux Christopher A O'Callaghan

Atherosclerosis 2016 07 2;250:95-105. Epub 2016 May 2.

Wellcome Trust Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, United Kingdom. Electronic address:

View Article

Download full-text PDF	Source
http://dx.doi.org/10.1016/j.atherosclerosis.2016.04.025	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917897	PMC

July 2016

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.

Authors:

Kyle J Gaulton Teresa Ferreira Yeji Lee Anne Raimondo Reedik Mägi Michael E Reschen Anubha Mahajan Adam Locke N William Rayner Neil Robertson Robert A Scott Inga Prokopenko Laura J Scott Todd Green Thomas Sparso Dorothee Thuillier Loic Yengo Harald Grallert Simone Wahl Mattias Frånberg Rona J Strawbridge Hans Kestler Himanshu Chheda Lewin Eisele Stefan Gustafsson Valgerdur Steinthorsdottir Gudmar Thorleifsson Lu Qi Lennart C Karssen Elisabeth M van Leeuwen Sara M Willems Man Li Han Chen Christian Fuchsberger Phoenix Kwan Clement Ma Michael Linderman Yingchang Lu Soren K Thomsen Jana K Rundle Nicola L Beer Martijn van de Bunt Anil Chalisey Hyun Min Kang Benjamin F Voight Gonçalo R Abecasis Peter Almgren Damiano Baldassarre Beverley Balkau Rafn Benediktsson Matthias Blüher Heiner Boeing Lori L Bonnycastle Erwin P Bottinger Noël P Burtt Jason Carey Guillaume Charpentier Peter S Chines Marilyn C Cornelis David J Couper Andrew T Crenshaw Rob M van Dam Alex S F Doney Mozhgan Dorkhan Sarah Edkins Johan G Eriksson Tonu Esko Elodie Eury João Fadista Jason Flannick Pierre Fontanillas Caroline Fox Paul W Franks Karl Gertow Christian Gieger Bruna Gigante Omri Gottesman George B Grant Niels Grarup Christopher J Groves Maija Hassinen Christian T Have Christian Herder Oddgeir L Holmen Astradur B Hreidarsson Steve E Humphries David J Hunter Anne U Jackson Anna Jonsson Marit E Jørgensen Torben Jørgensen Wen-Hong L Kao Nicola D Kerrison Leena Kinnunen Norman Klopp Augustine Kong Peter Kovacs Peter Kraft Jasmina Kravic Cordelia Langford Karin Leander Liming Liang Peter Lichtner Cecilia M Lindgren Eero Lindholm Allan Linneberg Ching-Ti Liu Stéphane Lobbens Jian'an Luan Valeriya Lyssenko Satu Männistö Olga McLeod Julia Meyer Evelin Mihailov Ghazala Mirza Thomas W Mühleisen Martina Müller-Nurasyid Carmen Navarro Markus M Nöthen Nikolay N Oskolkov Katharine R Owen Domenico Palli Sonali Pechlivanis Leena Peltonen John R B Perry Carl G P Platou Michael Roden Douglas Ruderfer Denis Rybin Yvonne T van der Schouw Bengt Sennblad Gunnar Sigurðsson Alena Stančáková Gerald Steinbach Petter Storm Konstantin Strauch Heather M Stringham Qi Sun Barbara Thorand Emmi Tikkanen Anke Tonjes Joseph Trakalo Elena Tremoli Tiinamaija Tuomi Roman Wennauer Steven Wiltshire Andrew R Wood Eleftheria Zeggini Ian Dunham Ewan Birney Lorenzo Pasquali Jorge Ferrer Ruth J F Loos Josée Dupuis Jose C Florez Eric Boerwinkle James S Pankow Cornelia van Duijn Eric Sijbrands James B Meigs Frank B Hu Unnur Thorsteinsdottir Kari Stefansson Timo A Lakka Rainer Rauramaa Michael Stumvoll Nancy L Pedersen Lars Lind Sirkka M Keinanen-Kiukaanniemi Eeva Korpi-Hyövälti Timo E Saaristo Juha Saltevo Johanna Kuusisto Markku Laakso Andres Metspalu Raimund Erbel Karl-Heinz Jöcke Susanne Moebus Samuli Ripatti Veikko Salomaa Erik Ingelsson Bernhard O Boehm Richard N Bergman Francis S Collins Karen L Mohlke Heikki Koistinen Jaakko Tuomilehto Kristian Hveem Inger Njølstad Panagiotis Deloukas Peter J Donnelly Timothy M Frayling Andrew T Hattersley Ulf de Faire Anders Hamsten Thomas Illig Annette Peters Stephane Cauchi Rob Sladek Philippe Froguel Torben Hansen Oluf Pedersen Andrew D Morris Collin N A Palmer Sekar Kathiresan Olle Melander Peter M Nilsson Leif C Groop Inês Barroso Claudia Langenberg Nicholas J Wareham Christopher A O'Callaghan Anna L Gloyn David Altshuler Michael Boehnke Tanya M Teslovich Mark I McCarthy Andrew P Morris

Nat Genet 2015 Dec 9;47(12):1415-25. Epub 2015 Nov 9.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF	Source
http://dx.doi.org/10.1038/ng.3437	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666734	PMC

December 2015

Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding.

Authors:

Michael E Reschen Kyle J Gaulton Da Lin Elizabeth J Soilleux Andrew J Morris Susan S Smyth Christopher A O'Callaghan

PLoS Genet 2015 Apr 2;11(4):e1005061. Epub 2015 Apr 2.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.

View Article

Download full-text PDF	Source
https://dx.plos.org/10.1371/journal.pgen.1005061	Publisher Site
http://dx.doi.org/10.1371/journal.pgen.1005061	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383549	PMC