팀:AllSeminarBioEMRxMutantSysBiolMAInfoJ.ClubTopicSemBookReading   발표자: All강성훈국수경권호식김나영김민정김재환김지헌문성희민유정배소정부은경안선주안세환유경훈유승원유승원유준기윤미선이시은인턴임성수전예진정문경조동영조민아조원일차재현채정환최선최선한봄허지허지연홍진희...AlexanderBaby Anusha SatravadaBaby Anusha SatravadaBaby Anusha SatravadaDesok KimHJInternJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young Jasmine CHOIJee-Young Jasmine CHOIJee-Young Jasmine CHOIJee-Young Jasmine Choi KelseyKwangsung AhnLiliaMike JacksonNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLPPPrabinRockySo Jeongabe torkeltonbenhjkyutest강기원강병희강병희강병희강석훈강소영고인석김경화김경화김기태김도균김동호김민구김보성김승빈김승호김영성김영훈김주연김주한김준호김지미김지훈김지희김진환김현대김형준김혜현김효정김효진나영지류영재민병주박원준박유랑박유미박은영박이영박정수박지연박지혜박찬희박호경백수연서명의서희원손경아송영수심재현심재현심혜진안빈안선주양웅철엄세인오가희우정훈윤선민윤영조이계화이수연이수연S이수현이우승이정우이정훈이현임영균임재현임준호전은주정상원정승원정용정태수정해원정희준조성범조용래주경민초빙강연최광윤최윤영최준영한미령한지예한현욱홍승권홍주영황동현源����������臾닿�����理���ㅼ��김기원김미현김세영김예진김옥구김윤희김지훈(H)박지연박지연변상재서화정신용준신현정온정헌윤혜성이석호이영주이정애이혜원임수아안성준권혜진유방암센터유수영유의혁(세종대)이권무황기태unknown세종대외부특강전체정혜림팀원권창혁송유림윤준희정제균   제목/키워드:    날짜:   

14	부은경	Assessment of variant combinatorial effects using multifactor-dimensionality reduction		TopicSem
31	부은경	Comparison of the multivariate genetic architecture of eight major psychiatric disorders across sex		J.Club

19	부은경	Identification of variant combinations that significantly affect PD susceptibility		TopicSem
29	부은경	GxGrare: gene-gene interaction analysis method for rare variants from high-throughput sequencing data		J.Club

05	부은경	Evaluating associations with variant combinations		TopicSem
22	부은경	Prioritizing effector genes at trait-associated loci using multimodal evidence		J.Club
26	부은경	Evaluating associations of variant combinations with PD		TopicSem

07	부은경	Pervasive biases in proxy genome-wide association studies based on parental history of Alzheimer’s disease		J.Club
19	부은경	Evaluating association of variant combinations with PD		TopicSem

02	부은경	Integration of variant annotations using deep set networks boosts rare variant association testing		J.Club
11	부은경			TopicSem
25	부은경	Exploring gene pairs potentially associated with Parkinson's disease		TopicSem

05	부은경	Exploration of gene pair distributions before and after permutation tests		TopicSem
21	부은경	Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK Biobank		J.Club
26	부은경	Enrichment analyses and modification of network graphs		TopicSem

08	부은경	Finding gene pairs specific to Parkinson’s disease		TopicSem
17	부은경	Gene selection by incorporating genetic networks into case-control association studies		J.Club

06	부은경	Calibrated prediction intervals for polygenic scores across diverse contexts		J.Club
29	부은경	Permutation tests of pgvb using PPMI dataset		TopicSem

02	부은경	Investigation of the properties of GVB-based PD network		TopicSem
25	부은경	Genetic mapping across autoimmune diseases reveals shared associations and mechanisms		J.Club
30	부은경	Ideas to interpret the pair-GVB based network		TopicSem

11	부은경	Exploration of characteristics in clusters of PD		TopicSem
20	부은경	Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease		J.Club

16	부은경	Inferring compound heterozygosity from large-scale exome sequencing data		J.Club
21	부은경	Analysis of trends among k-cores for understanding PD		TopicSem

15	부은경	Variant- and gene-wise analyses in Parkinson’s Disease		TopicSem
27	부은경	Network-guided search for genetic heterogeneity between gene pairs		J.Club

09	부은경	Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder		J.Club
18	부은경	Clinical variable selection strategies for prediction modelling		TopicSem

11	부은경	Age-dependent topic modeling of comorbidities in UK Biobank identifies disease subtypes with differential genetic risk		J.Club
23	부은경	Regression analysis in Parkinson’s disease		TopicSem

07	부은경	Variant- and gene-wise analyses of Parkinson’s disease		TopicSem
16	부은경	Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies		J.Club

05	부은경	Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases		J.Club
14	부은경	Variant- and gene-wise analyses of PD		TopicSem

17	부은경	Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine		J.Club
22	부은경	Pair gvb-based network analysis in parkinson’s disease		TopicSem

04	부은경	Progress of pair-gvb analysis in PD patients		TopicSem
13	부은경	Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models		J.Club
25	부은경	Single- and pair-gvb analysis in Parkinson’s disease		TopicSem

13	부은경	Study design using PWGVB in patients with PD		TopicSem
25	부은경	Network expansion of genetic associations defines a pleiotropy map of human cell biology		J.Club

06	부은경	PPMI Data Overview		TopicSem
11	부은경	Pairwise effects between lipid GWAS genes modulate lipid plasma levels and cellular uptake		J.Club

03	부은경	An integral genomic signature approach for tailored cancer therapy using genome-wide sequencing data		J.Club
08	부은경	Evaluation of pharmacogenetic influences on thiopurine-induced leukopenia in patients with inflammatory bowel disease (Results)		TopicSem

06	부은경	Evaluation of pharmacogenetic influences on thiopurine-induced leukopenia in patients with inflammatory bowel disease(Methods)		TopicSem
24	부은경	.		SysBiol
29	부은경	Integrative analysis of drug response and clinical outcome in acute myeloid leukemia		J.Club

01	부은경	Evaluation of association between genetic variants and thiopurine-induced leukopenia in inflammatory bowel disease		TopicSem
24	부은경	Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility		J.Club

11	부은경	Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study		J.Club
16	부은경	Effect of IFX on the associations between genetic variants and thiopurine-induced leukopenia		TopicSem

05	부은경	Exploration of genotype-phenotype interactions and prevalence of genetic variants		SysBiol
11	부은경	Figures for association between genetic variantsand TILin IBD patients		TopicSem
23	부은경	New insights into the genetic etiology of Alzheimer’s disease and related dementias		J.Club
28	부은경	Summary of evaluation of association between TIL and genetic risk factors in IBD		TopicSem

10	부은경	Evaluation of association between genetic variants and leukopenia in IBD patients using survival analysis		TopicSem
19	부은경	Whole-genome sequencing in diverse subjectsidentifies genetic correlates of leukocyte traits:The NHLBI TOPMed program		J.Club

09	부은경	Comparison of thiopurine-induced leukopenia incidence among genetic subgroups in IBD patients		TopicSem
14	부은경	Study ideas for analyzing recurrent event data and correcting potential bias		SysBiol
18	부은경	A polygenic-score-based approach for identification of gene-drug interactions stratifying breast cancer risk		J.Club

21	부은경	Evaluation of association between genetic variants and TIL in 3 IBD datasets		TopicSem
30	부은경	Polygenic basis and biomedical consequences of telomere length variation		J.Club

05	부은경	Genetic variants that increase susceptibility to thiopurine-induced leukopenia in IBD patients		TopicSem
10	부은경	Survival Analysis Using Frailty Models		SysBiol
28	부은경	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses		J.Club

12	부은경	Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson’s disease		J.Club
28	부은경	Association between genetic variants and Thiopurine-induced leukopenia in IBD patients		TopicSem

01	부은경	Genetics of 35 blood and urine biomarkers in the UK Biobank		J.Club
13	부은경	Association between genetic variants and Thiopurine-induced adverse reactions in IBD patients		TopicSem

13	부은경	Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture		J.Club
18	부은경	Additional data for interpreting thiopurine intolerance in patients with IBD		TopicSem
23	부은경	PGx of Inflammatory Bowel Disease		Seminar

11	부은경	Comparison of clinical outcomes according to pharmacogenetic information		TopicSem
23	부은경	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals		J.Club

09	부은경	Variant-level explanation for gender difference in PD		TopicSem
12	부은경	FastTargetPred: a program enabling the fast prediction of putative protein targets for input chemical databases		SysBiol
21	부은경	Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy		J.Club
30	부은경	Classification of IBD subjects into three types of drug metabolizers		TopicSem

12	부은경	Validation of PD-associated Variants Using UKBB data		TopicSem
24	부은경	Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale		J.Club

08	부은경	High-definition likelihood inference of genetic correlations across human complex traits		J.Club
20	부은경	Summary of Candidate PD-associated Variants and Plan for Validation		TopicSem

21	부은경	Comparison of genetic loads between males and females with PD		TopicSem
30	부은경	Complementary genes contribute sex-biased vulnerability in diverse disorders		J.Club

04	부은경	Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk		J.Club
23	부은경			TopicSem

22

부은경

Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts

J.Club

07	부은경	Gender Differences in Parkinson’s Disease		TopicSem
30	부은경	Discovering personalized driver mutation profiles of single samples in cancer by network control strategy		J.Club

26	부은경	Identifying Gender-Specific Variants in Parkinson		TopicSem
28	부은경	Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing		J.Club

06	부은경	Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk		J.Club
11	부은경	PPMI WES Data Overview and Analysis Plan		TopicSem

04	부은경	Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma		J.Club
30	부은경	Multiple Myeloma: Data Preprocessing		TopicSem