Yale University

University / College


Location: New Haven, CT, United States (USA) (US) US

ISNI: 0000000419368710

ROR: https://ror.org/03v76x132

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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Unpublished / Preprint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

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To

Abstract

Journal

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome (2018) Braun DA, Lovric S, Schapiro D, Schneider R, Marquez J, Asif M, Hussain MS, et al. Journal article Braided Tensor Categories of Admissible Modules for Affine Lie Algebras (2018) Creutzig T, Huang YZ, Yang J Journal article Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract (2018) Van Der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, et al. Journal article GAPVD1 and ANKFY1 mutations implicate RAB5 regulation in nephrotic syndrome (2018) Hermle T, Schneider R, Schapiro D, Braun DA, Van Der Ven AT, Warejko JK, Daga A, et al. Journal article Impact of global mean normalization on regional glucose metabolism in the human brain (2018) Mortensen KN, Gjedde A, Thompson GJ, Herman P, Paret MJ, Rothman DL, Kupers R, et al. Journal article Mental health assessment of altruistic non-directed kidney donors: An EAPM consensus statement. (2018) Potts S, Vitinius F, Erim Y, Gazdag G, Gribble R, Ismail SY, Massey EK, et al. Journal article, Original article Quantum theory of continuum optomechanics (2018) Rakich P, Marquardt F Journal article Statistical Shape Modeling of the Left Ventricle: Myocardial Infarct Classification Challenge (2018) Suinesiaputra A, Ablin P, Alba X, Alessandrini M, Allen J, Bai W, Cimen S, et al. Journal article A cross-sectional study assessing the association between online ratings and clinical quality of care measures for US hospitals: results from an observational study. (2018) Emmert M, Meszmer N, Schlesinger M Journal article, Original article Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis (2018) Daga A, Majmundar AJ, Braun DA, Gee HY, Lawson JA, Shril S, Jobst-Schwan T, et al. Journal article