Suchergebnisse - "Hu, Fengyuan"

PubPharm (32)

11

A minimal role for synonymous variation in human disease

enthalten in: bioRxiv.org | 2022

von Dhindsa, R. | Wang, Q. | Vitsios, D. | +7

12

HumanMine : advanced data searching, analysis and cross-species comparison

enthalten in: Database : the journal of biological databases and curation | 2022

von Lyne, R. | Bazaga, A. | Butano, D. | +11

13

Correction to : ORFLine: a bioinformatic pipeline to prioritize small open reading frames identifies candidate secreted small proteins from lymphocytes

enthalten in: Bioinformatics (Oxford, England) | 2022

von Hu, F. | Lu, J. | Matheson, L. | +3

ErratumFor: Bioinformatics. 2021 May 10;:. - PMID 33970232

14

ORFLine: a bioinformatic pipeline to prioritise small open reading frames identifies candidate secreted small proteins from lymphocytes

enthalten in: bioRxiv.org | 2021

von Hu, F. | Lu, J. | Munoz, M. | +2

15

ORFLine : a bioinformatic pipeline to prioritize small open reading frames identifies candidate secreted small proteins from lymphocytes

enthalten in: Bioinformatics (Oxford, England) | 2021

von Hu, F. | Lu, J. | Matheson, L. | +4

ErratumIn: Bioinformatics. 2022 Mar 29;:null. - PMID 35349648

16

Rare variant contribution to human disease in 281,104 UK Biobank exomes

enthalten in: Nature | 2021

von Wang, Q. | Dhindsa, R. | Carss, K. | +57

17

Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

enthalten in: The Journal of allergy and clinical immunology | 2020

von Lorenzini, T. | Fliegauf, M. | Klammer, N. | +173

ErratumIn: J Allergy Clin Immunol. 2021 Nov;148(5):1345. - PMID 34743834

18

Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children

enthalten in: Intensive care medicine | 2019

von French, C. | Delon, I. | Dolling, H. | +81

19

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

enthalten in: Blood | 2016

von Simeoni, I. | Stephens, J. | Hu, F. | +76

CommentIn: Blood. 2016 Jun 9;127(23 ):2781-2. - PMID 27282940

20

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

enthalten in: Blood | 2016

von Simeoni, I. | Stephens, J. | Hu, F. | +76