Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits (vol 12, 108, 2019)

被引：0

作者：

Glicksberg, Benjamin S. ^{[1
,2
,15
]}

Amadori, Letizia ^{[1
,3
,4
]}

Akers, Nicholas K. ^{[1
]}

Sukhavasi, Katyayani ^{[5
]}

Franzen, Oscar ^{[1
,6
,16
]}

Li, Li ^{[1
,2
]}

Belbin, Gillian M. ^{[1
,7
]}

Ayers, Kristin L. ^{[1
,8
]}

Shameer, Khader ^{[1
,2
]}

Badgeley, Marcus A. ^{[1
,2
]}

Johnson, Kipp W. ^{[1
,2
]}

Readhead, Ben ^{[1
,2
]}

Darrow, Bruce J. ^{[3
,4
]}

Kenny, Eimear E. ^{[7
,9
]}

Betsholtz, Christer ^{[10
]}

Ermel, Raili ^{[11
]}

Skogsberg, Josefin ^{[12
]}

Ruusalepp, Arno ^{[6
,10
]}

Schadt, Eric E. ^{[1
,2
,6
,8
]}

Dudley, Joel T. ^{[1
,2
,13
]}

Ren, Hongxia ^{[14
]}

Kovacic, Jason C. ^{[3
,4
]}

Giannarelli, Chiara ^{[1
,3
,4
]}

Li, Shuyu D. ^{[1
,8
]}

Bjorkegren, Johan L. M. ^{[1
,5
,6
,12
]}

Chen, Rong ^{[1
,8
]}

机构：

[1] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, Icahn Inst Genom & Multiscale Biol, One Gustave L Levy Pl, New York, NY 10029 USA

[2] Icahn Sch Med Mt Sinai, Inst Next Generat Healthcare, One Gustave L Levy Pl, New York, NY 10029 USA

[3] Icahn Sch Med Mt Sinai, Cardiovasc Res Ctr, One Gustave L Levy Pl, New York, NY 10029 USA

[4] Icahn Sch Med Mt Sinai, Cardiovasc Inst, One Gustave L Levy Pl, New York, NY 10029 USA

[5] Univ Tartu, Dept Pathophysiol, Inst Biomed & Translat Med, Biomeedikum, Ravila 19, EE-50411 Tartu, Estonia

[6] Clin Gene Networks AB, Jungfrugatan 10, S-11444 Stockholm, Sweden

[7] Icahn Sch Med Mt Sinai, Charles Bronfman Inst Personalized Med, One Gustave L Levy Pl, New York, NY 10029 USA

[8] Sema4, Stamford, CT 06902 USA

[9] Icahn Sch Med Mt Sinai, Dept Prevent Med, One Gustave L Levy Pl, New York, NY 10029 USA

[10] Uppsala Univ, Dept Immunol Genet & Pathol, S-75185 Uppsala, Sweden

[11] Tartu Univ Hosp, Dept Cardiac Surg, 1a Ludwig Puusepa St, EE-50406 Tartu, Estonia

[12] Karolinska Inst, Integrated Cardio Metab Ctr, Dept Med, Karolinska Univ Sjukhuset Huddinge, S-14186 Stockholm, Sweden

[13] Icahn Sch Med Mt Sinai, Dept Hlth Policy & Res, One Gustave L Levy Pl, New York, NY 10029 USA

[14] Indiana Univ, Herman B Wells Ctr Pediat Res, Ctr Diabet & Metab Dis, Dept Pediat,Stark Neurosci Res Inst, 635 Barnhill Dr,MS2049, Indianapolis, IN 46202 USA

[15] Univ Calif San Francisco, Bakar Computat Hlth Sci Inst, San Francisco, CA 94158 USA

[16] Karolinska Inst, Integrated Cardio Metab Ctr, Dept Med, S-14157 Huddinge, Sweden

来源：

BMC MEDICAL GENOMICS | 2019年 / 12卷 / 01期

关键词：

D O I：

10.1186/s12920-019-0573-9

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页数：1

共 12 条

[1] Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits
Benjamin S. Glicksberg
Letizia Amadori
Nicholas K. Akers
Katyayani Sukhavasi
Oscar Franzén
Li Li
Gillian M. Belbin
Kristin L. Akers
Khader Shameer
Marcus A. Badgeley
Kipp W. Johnson
Ben Readhead
Bruce J. Darrow
Eimear E. Kenny
Christer Betsholtz
Raili Ermel
Josefin Skogsberg
Arno Ruusalepp
Eric E. Schadt
Joel T. Dudley
Hongxia Ren
Jason C. Kovacic
Chiara Giannarelli
Shuyu D. Li
Johan L. M. Björkegren
Rong Chen
BMC Medical Genomics, 12
[2] Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits
Glicksberg, Benjamin S.
Amadori, Letizia
Akers, Nicholas K.
Sukhavasi, Katyayani
Franzen, Oscar
Li, Li
Belbin, Gillian M.
Akers, Kristin L.
Shameer, Khader
Badgeley, Marcus A.
Johnson, Kipp W.
Readhead, Ben
Darrow, Bruce J.
Kenny, Eimear E.
Betsholtz, Christer
Ermel, Raili
Skogsberg, Josefin
Ruusalepp, Arno
Schadt, Eric E.
Dudleyt, Joel T.
Ren, Hongxia
Kovacic, Jason C.
Giannarelli, Chiara
Liu, Shuyu D.
Bjorkegren, Johan L. M.
Chen, Rong
BMC MEDICAL GENOMICS, 2019, 12 (Suppl 6)
[3] Correction to: Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits
Benjamin S. Glicksberg
Letizia Amadori
Nicholas K. Akers
Katyayani Sukhavasi
Oscar Franzén
Li Li
Gillian M. Belbin
Kristin L. Ayers
Khader Shameer
Marcus A. Badgeley
Kipp W. Johnson
Ben Readhead
Bruce J. Darrow
Eimear E. Kenny
Christer Betsholtz
Raili Ermel
Josefin Skogsberg
Arno Ruusalepp
Eric E. Schadt
Joel T. Dudley
Hongxia Ren
Jason C. Kovacic
Chiara Giannarelli
Shuyu D. Li
Johan L. M. Björkegren
Rong Chen
BMC Medical Genomics, 12
[4] Comprehensive functional analysis of chymotrypsin C (CTRC) variants reveals distinct loss-of-function mechanisms associated with pancreatitis risk
Beer, Sebastian
Zhou, Jiayi
Szabo, Andras
Keiles, Steven
Chandak, Giriraj Ratan
Witt, Heiko
Sahin-Toth, Miklos
GUT, 2013, 62 (11) : 1616 - 1624
[5] Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants
Griswold, Anthony J.
Dueker, Nicole D.
Van Booven, Derek
Rantus, Joseph A.
Jaworski, James M.
Slifer, Susan H.
Schmidt, Michael A.
Hulme, William
Konidari, Ioanna
Whitehead, Patrice L.
Cuccaro, Michael L.
Martin, Eden R.
Haines, Jonathan L.
Gilbert, John R.
Hussman, John P.
Pericak-Vance, Margaret A.
MOLECULAR AUTISM, 2015, 6
[6] QTL analysis reveals genomic variants linked to high-temperature fermentation performance in the industrial yeast (vol 12, 59, 2019)
Wang, Zhen
Qi, Qi
Lin, Yuping
Guo, Yufeng
Liu, Yanfang
Wang, Qinhong
BIOTECHNOLOGY FOR BIOFUELS, 2019, 12 (1)
[7] Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants
Anthony J. Griswold
Nicole D. Dueker
Derek Van Booven
Joseph A. Rantus
James M. Jaworski
Susan H. Slifer
Michael A. Schmidt
William Hulme
Ioanna Konidari
Patrice L. Whitehead
Michael L. Cuccaro
Eden R. Martin
Jonathan L. Haines
John R. Gilbert
John P. Hussman
Margaret A. Pericak-Vance
Molecular Autism, 6
[8] Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease (vol 17, e1009679, 2021)
Audain, Enrique
Wilsdon, Anna
Breckpot, Jeroen
Izarzugaza, Jose M. G.
Fitzgerald, Tomas W.
Kahlert, Anne-Karin
Sifrim, Alejandro
Wunnemann, Florian
Perez-Riverol, Yasset
Abdul-Khaliq, Hashim
Bak, Mads
Bassett, Anne S.
Benson, D. Woodrow
Berger, Felix
Daehnert, Ingo
Devriendt, Koenraad
Dittrich, Sven
Daubeney, Piers E. F.
Garg, Vidu
Hackmann, Karl
Hoff, Kirstin
Hofmann, Philipp
Dombrowsky, Gregor
Pickardt, Thomas
Bauer, Ulrike
Keavney, Bernard D.
Klaassen, Sabine
Kramer, Hans-Heiner
Marshall, Christian R.
Milewicz, Dianna M.
Lemaire, Scott
Coselli, Joseph S.
Mitchell, Michael E.
Tomita-Mitchell, Aoy
Prakash, Siddharth K.
Stamm, Karl
Stewart, Alexandre F. R.
Silversides, Candice K.
Siebert, Reiner
Stiller, Brigitte
Rosenfeld, Jill A.
Vater, Inga
Postma, Alex V.
Caliebe, Almuth
Brook, J. David
Andelfinger, Gregor
Hurles, Matthew E.
Thienpont, Bernard
Larsen, Lars Allan
Hitz, Marc-Phillip
PLOS GENETICS, 2021, 17 (09):
[9] An integrative transcriptomic and genomic analysis reveals novel insights into the hub genes and regulatory networks associated with rubber synthesis in H. brasiliensis
Ding, Zehong
Fu, Lili
Tan, Deguan
Sun, Xuepiao
Zhang, Jiaming
INDUSTRIAL CROPS AND PRODUCTS, 2020, 153 (153)
[10] Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (vol 15, 22, 2023)
Matuozzo, Daniela
Talouarn, Estelle
Marchal, Astrid
Zhang, Peng
Manry, Jeremy
Seeleuthner, Yoann
Zhang, Yu
Bolze, Alexandre
Chaldebas, Matthieu
Milisavljevic, Baptiste
Gervais, Adrian
Bastard, Paul
Asano, Takaki
Bizien, Lucy
Barzaghi, Federica
Abolhassani, Hassan
Tayoun, Ahmad Abou
Aiuti, Alessandro
Darazam, Ilad Alavi
Allende, Luis M.
Alonso-Arias, Rebeca
Arias, Andres Augusto
Aytekin, Gokhan
Bergman, Peter
Bondesan, Simone
Bryceson, Yenan T.
Bustos, Ingrid G.
Cabrera-Marante, Oscar
Carcel, Sheila
Carrera, Paola
Casari, Giorgio
Chaibi, Khalil
Colobran, Roger
Condino-Neto, Antonio
Covill, Laura E.
Delmonte, Ottavia M.
Zein, Loubna El
Flores, Carlos
Gregersen, Peter K.
Gut, Marta
Haerynck, Filomeen
Halwani, Rabih
Hancerli, Selda
Hammarstroem, Lennart
Hatipoglu, Nevin
Karbuz, Adem
Keles, Sevgi
Kyheng, Christele
Leon-Lopez, Rafael
Franco, Jose Luis
GENOME MEDICINE, 2024, 16 (01)

← 1 2 →