University of Cambridge

University / College


Location: Cambridge, United Kingdom (GB) GB

ISNI: 0000000121885934

ROR: https://ror.org/013meh722

Show on Map:


close-button

Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents (2016) Khetarpal SA, Schjoldager KT, Christoffersen C, Raghavan A, Edmondson AC, Reutter HM, Ahmed B, et al. Journal article Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer (2016) Hampras SS, Sucheston-Campbell LE, Cannioto R, Chang-Claude J, Modugno F, Doerk T, Hillemanns P, et al. Journal article Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia (2016) Meyer E, Carss KJ, Rankin J, Nichols JME, Grozeva D, Joseph AP, Mencacci NE, et al. Journal article GRS 1739-278 Observed at Very Low Luminosity with XMM-Newton and NuSTAR (2016) Furst F, Tomsick JA, Yamaoka K, Dauser T, Miller JM, Clavel M, Corbel S, et al. Journal article ATI718PLUS® - New nickel based disc alloy and its capability (2016) Huenert D, Pröbstle M, Casanova A, Schlütter R, Krakow R, Büscher M, Randelzhofer P, et al. Conference contribution, Conference Contribution SPECTRO-TIMING STUDY of GX 339-4 in A HARD INTERMEDIATE STATE (2016) Furst F, Grinberg V, Tomsick JA, Bachetti M, Boggs SE, Brightman M, Christensen FE, et al. Journal article, Original article Athena Wide Field Imager key science drivers (2016) Rau A, Nandra K, Aird J, Comastri A, Dauser T, Merloni A, Pratt GW, et al. Conference contribution, Conference Contribution Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status (2016) Luedeke M, Rinckleb AE, Fitzgerald LM, Geybels MS, Schleutker J, Eeles RA, Teixeira MR, et al. Journal article Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum (2016) Smogavec M, Cleall A, Hoyer J, Lederer D, Nassogne MC, Palmer EE, Deprez M, et al. Journal article Variational Depth from Focus Reconstruction (2015) Moeller M, Benning M, Schoenlieb C, Cremers D Journal article