A Systematic Approach for Identifying Causal Variants and Their Target Genes on JIA Risk Haplotypes

被引：0

作者：

Jiang, Kaiyu ^{[1
]}

liu, tao ^{[2
]}

Tewhey, Ryan ^{[3
]}

Kales, Susan ^{[3
]}

Park, Yungki ^{[4
]}

Jarvis, James N. ^{[5
]}

机构：

[1] SUNY Buffalo, Buffalo, NY USA

[2] Roswell Pk Canc Inst, Buffalo, NY USA

[3] Jackson Labs, Bar Harbor, ME USA

[4] SUNY Buffalo, Jacobs Sch Med & Biomed Sci, Buffalo, NY USA

[5] SUNY Buffalo, Jacobs Sch Med, Buffalo, NY USA

来源：

ARTHRITIS & RHEUMATOLOGY | 2023年 / 75卷

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

0031

引用

页码：51 / 52

页数：2

共 50 条

[31] Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach
Versmissen, Jorie
Oosterveer, Daniella M.
Yazdanpanah, Mojgan
Dehghan, Abbas
Holm, Hilma
Erdman, Jeanette
Aulchenko, Yurii S.
Thorleifsson, Gudmar
Schunkert, Heribert
Huijgen, Roeland
Vongpromek, Ranitha
Uitterlinden, Andre G.
Defesche, Joep C.
van Duijn, Cornelia M.
Mulder, Monique
Dadd, Tony
Karlsson, Hrobjartur D.
Ordovas, Jose
Kindt, Iris
Jarman, Amelia
Hofman, Albert
van Vark-van der Zee, Leonie
Blommesteijn-Touw, Adriana C.
Kwekkeboom, Jaap
Liem, Anho H.
van der Ouderaa, Frans J.
Calandra, Sebastiano
Bertolini, Stefano
Averna, Maurizio
Langslet, Gisle
Ose, Leiv
Ros, Emilio
Almagro, Fatima
de Leeuw, Peter W.
Civeira, Fernando
Masana, Luis
Pinto, Xavier
Simoons, Maarten L.
Schinkel, Arend F. L.
Green, Martin R.
Zwinderman, Aeilko H.
Johnson, Keith J.
Schaefer, Arne
Neil, Andrew
Witteman, Jacqueline C. M.
Humphries, Steve E.
Kastelein, John J. P.
Sijbrands, Eric J. G.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (03) : 381 - 387
[32] Identifying causal risk factors of metabolic syndrome for renal cell carcinoma. A Mendelian randomization approach
Carreras-Torres, Robert
Johansson, Mattias
Scelo, Ghislaine
Haycock, Philip
Purdue, Mark
Wu, Xifeng
Houlston, Richard
Chanock, Stephen
Brennan, Paul
CANCER RESEARCH, 2016, 76
[33] IL-27 variants might be genetic risk factors for preeclampsia: based on genetic polymorphisms, haplotypes and in silico approach
Jahantigh, Danial
Ghazaey Zidanloo, Saeedeh
Forghani, Forough
Doroudian, Mohammad
MOLECULAR BIOLOGY REPORTS, 2020, 47 (10) : 7929 - 7940
[34] Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Aragam, Krishna G.
Jiang, Tao
Goel, Anuj
Kanoni, Stavroula
Wolford, Brooke N.
Atri, Deepak S.
Weeks, Elle M.
Wang, Minxian
Hindy, George
Zhou, Wei
Grace, Christopher
Roselli, Carolina
Marston, Nicholas A.
Kamanu, Frederick K.
Surakka, Ida
Venegas, Loreto Munoz
Sherliker, Paul
Koyama, Satoshi
Ishigaki, Kazuyoshi
Asvold, Bjorn O.
Brown, Michael R.
Brumpton, Ben
de Vries, Paul S.
Giannakopoulou, Olga
Giardoglou, Panagiota
Gudbjartsson, Daniel F.
Gueldener, Ulrich
Haider, Syed M. Ijlal
Helgadottir, Anna
Ibrahim, Maysson
Kastrati, Adnan
Kessler, Thorsten
Kyriakou, Theodosios
Konopka, Tomasz
Li, Ling
Ma, Lijiang
Meitinger, Thomas
Mucha, Soeren
Munz, Matthias
Murgia, Federico
Nielsen, Jonas B.
Noethen, Markus M.
Pang, Shichao
Reinberger, Tobias
Schnitzler, Gavin
Smedley, Damian
Thorleifsson, Gudmar
von Scheidt, Moritz
Ulirsch, Jacob C.
Arnar, David O.
NATURE GENETICS, 2022, 54 (12) : 1803 - 1815
[35] IL-27 variants might be genetic risk factors for preeclampsia: based on genetic polymorphisms, haplotypes and in silico approach
Danial Jahantigh
Saeedeh Ghazaey Zidanloo
Forough Forghani
Mohammad Doroudian
Molecular Biology Reports, 2020, 47 : 7929 - 7940
[36] Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Krishna G. Aragam
Tao Jiang
Anuj Goel
Stavroula Kanoni
Brooke N. Wolford
Deepak S. Atri
Elle M. Weeks
Minxian Wang
George Hindy
Wei Zhou
Christopher Grace
Carolina Roselli
Nicholas A. Marston
Frederick K. Kamanu
Ida Surakka
Loreto Muñoz Venegas
Paul Sherliker
Satoshi Koyama
Kazuyoshi Ishigaki
Bjørn O. Åsvold
Michael R. Brown
Ben Brumpton
Paul S. de Vries
Olga Giannakopoulou
Panagiota Giardoglou
Daniel F. Gudbjartsson
Ulrich Güldener
Syed M. Ijlal Haider
Anna Helgadottir
Maysson Ibrahim
Adnan Kastrati
Thorsten Kessler
Theodosios Kyriakou
Tomasz Konopka
Ling Li
Lijiang Ma
Thomas Meitinger
Sören Mucha
Matthias Munz
Federico Murgia
Jonas B. Nielsen
Markus M. Nöthen
Shichao Pang
Tobias Reinberger
Gavin Schnitzler
Damian Smedley
Gudmar Thorleifsson
Moritz von Scheidt
Jacob C. Ulirsch
David O. Arnar
Nature Genetics, 2022, 54 : 1803 - 1815
[37] Reverse PCA, a Systematic Approach for Identifying Genes Important for the Physical Interaction between Protein Pairs
Lev, Ifat
Volpe, Marina
Goor, Liron
Levinton, Nelly
Emuna, Liach
Ben-Aroya, Shay
PLOS GENETICS, 2013, 9 (10):
[38] Uncovering the functional variants and target genes of the 7q32 pancreatic cancer risk locus
O'Brien, Aidan
Hoskins, Jason W.
Eiser, Daina R.
Connelly, Katelyn E.
Zhong, Jun
Andresson, Thorkell
Collins, Irene
Chanock, Stephen J.
Klein, Alison P.
Arda, H. Efsun
Amundadottir, Laufey T.
CANCER RESEARCH, 2022, 82 (12)
[39] Single-Nucleotide Variants in microRNAs Sequences or in their Target Genes Might Influence the Risk of Epilepsy: A Review
Renata Parissi Buainain
Matheus Negri Boschiero
Bruno Camporeze
Paulo Henrique Pires de Aguiar
Fernando Augusto Lima Marson
Manoela Marques Ortega
Cellular and Molecular Neurobiology, 2022, 42 : 1645 - 1658
[40] Chromatin architecture reveals cell type-specific target genes for kidney disease risk variants
Aiping Duan
Hong Wang
Yan Zhu
Qi Wang
Jing Zhang
Qing Hou
Yuexian Xing
Jinsong Shi
Jinhua Hou
Zhaohui Qin
Zhaohong Chen
Zhihong Liu
Jingping Yang
BMC Biology, 19

← 1 2 3 4 5 →