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Unpublished / Preprint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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Abstract

Journal

Whole-Exome sequencing enables a precision medicine approach for kidney transplant recipients (2019) Mann N, Braun DA, Amann K, Tan W, Shril S, Connaughton DM, Nakayama M, et al. Journal article Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility Locus (2019) Buckley MA, Woods NT, Tyrer JP, Mendoza-Fandino G, Lawrenson K, Hazelett DJ, Najafabadi HS, et al. Journal article The human lung cell atlas: A high-resolution reference map of the human lung in health and disease (2019) Schiller HB, Montoro DT, Simon LM, Rawlins EL, Meyer KB, Strunz M, Braga FAV, et al. Journal article, Review article Correction to: Gap Analysis Regarding Prognostication in Neurocritical Care: A Joint Statement from the German Neurocritical Care Society and the Neurocritical Care Society (2019) Wartenberg KE, Hwang DY, Haeusler KG, Muehlschlegel S, Sakowitz OW, Madžar D, Hamer H, et al. Journal article, Erratum Gap Analysis Regarding Prognostication in Neurocritical Care: A Joint Statement from the German Neurocritical Care Society and the Neurocritical Care Society (2019) Wartenberg KE, Hwang DY, Häusler KG, Muehlschlegel S, Sakowitz OW, Madžar D, Hamer H, et al. Journal article Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children (2019) Vivante A, Chacham OS, Shril S, Schreiber R, Mane SM, Pode-Shakked B, Soliman NA, et al. Journal article Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment (2018) Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, et al. Journal article 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