Detalhe da pesquisa
1.
Somatic Evolution in Non-neoplastic IBD-Affected Colon.
Cell
; 182(3): 672-684.e11, 2020 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32697969
2.
Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway.
Cell
; 155(1): 57-69, 2013 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24035192
3.
shaPRS: Leveraging shared genetic effects across traits or ancestries improves accuracy of polygenic scores.
Am J Hum Genet
; 2024 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38703768
4.
Somatic mutations provide important and unique insights into the biology of complex diseases.
Trends Genet
; 37(10): 872-881, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34226062
5.
An Integrated Taxonomy for Monogenic Inflammatory Bowel Disease.
Gastroenterology
; 162(3): 859-876, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34780721
6.
Fine-mapping inflammatory bowel disease loci to single-variant resolution.
Nature
; 547(7662): 173-178, 2017 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-28658209
7.
Common and Rare Variant Prediction and Penetrance of IBD in a Large, Multi-ethnic, Health System-based Biobank Cohort.
Gastroenterology
; 160(5): 1546-1557, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33359885
8.
Rapid at-line early cell death quantification using capacitance spectroscopy.
Biotechnol Bioeng
; 119(3): 857-867, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34927241
9.
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
; 15(5): e1008190, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31145742
10.
HLA-DQA1*05 Carriage Associated With Development of Anti-Drug Antibodies to Infliximab and Adalimumab in Patients With Crohn's Disease.
Gastroenterology
; 158(1): 189-199, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31600487
11.
Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis.
PLoS Genet
; 14(12): e1007833, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30507971
12.
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
; 14(5): e1007329, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29795570
13.
Terahertz Time of Flight Spectroscopy as a Coating Thickness Reference Method for Partial Least Squares Near Infrared Spectroscopy Models.
Anal Chem
; 92(5): 3658-3665, 2020 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32020798
14.
Factors Associated With Outcomes of Patients With Primary Sclerosing Cholangitis and Development and Validation of a Risk Scoring System.
Hepatology
; 69(5): 2120-2135, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30566748
15.
Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease.
JAMA
; 321(8): 773-785, 2019 02 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30806694
16.
Feedforward and Feedback Control of a Pharmaceutical Coating Process.
AAPS PharmSciTech
; 20(4): 157, 2019 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30937727
17.
Method Development and Validation of an Inline Process Analytical Technology Method for Blend Monitoring in the Tablet Feed Frame Using Raman Spectroscopy.
Anal Chem
; 90(14): 8436-8444, 2018 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-29905065
18.
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Nature
; 491(7422): 119-24, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23128233
19.
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.
Am J Hum Genet
; 94(2): 295-302, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24462371
20.
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.
Am J Hum Genet
; 94(6): 915-23, 2014 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24906020