EXOME SEQUENCING OF MULTIPLY AFFECTED BIPOLAR DISORDER FAMILIES AND FOLLOW-UP RESEQUENCING IMPLICATE RARE VARIANTS IN NEURONAL GENES CONTRIBUTING TO DISEASE ETIOLOGY

被引：0

作者：

Forstner, Andreas J. ^{[1
]}

Maaser, Anna ^{[1
]}

Strohmaier, Jana ^{[2
]}

Ludwig, Kerstin U. ^{[1
]}

Degenhardt, Franziska ^{[1
]}

Streit, Fabian ^{[2
]}

Thiele, Holger ^{[3
]}

Nuernberg, Peter ^{[3
]}

Herms, Stefan ^{[1
,4
]}

Hoffmann, Per ^{[1
,4
]}

Cichon, Sven ^{[1
,4
]}

Rietschel, Marcella ^{[5
]}

Noethen, Markus M. ^{[1
]}

机构：

[1] Univ Bonn, Bonn, Germany

[2] Heidelberg Univ, Med Fac Mannheim, Heidelberg, Germany

[3] Univ Cologne, Cologne Ctr Genom, Cologne, Germany

[4] Univ Basel, Basel, Switzerland

[5] Heidelberg Univ, Med Fac Mannheim, Cent Inst Mental Hlth, Heidelberg, Germany

来源：

EUROPEAN NEUROPSYCHOPHARMACOLOGY | 2019年 / 29卷

关键词：

D O I：

10.1016/j.euroneuro.2017.08.099

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

SA27

引用

页码：S836 / S837

页数：2

共 17 条

[1] Exome sequencing of multiply affected bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology
Maaser, A.
Strohmaier, J.
Ludwig, K. U.
Degenhardt, F.
Streit, F.
Schenk, L. M.
Koller, A. C.
Fischer, S. B.
Thiele, H.
Nuernberg, P.
Guzman-Parra, J.
Orozco Diaz, G.
Auburger, G.
Albus, M.
Borrmann-Hassenbach, M.
Jose Gonzalez, M.
Gil Flores, S.
Cabaleiro Fabeiro, F. J.
del Rio Noriega, F.
Perez Perez, F.
Haro Gonzalez, J.
Rivas, F.
Mayoral, F.
Herms, S.
Hoffmann, P.
Cichon, S.
Rietschel, M.
Noethen, M. M.
Forstner, A. J.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 373 - 374
[2] Exome sequencing of multiplex bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology
Maaser, A.
Strohmaier, J.
Ludwig, K. U.
Henschel, L.
Streit, F.
Degenhardt, F.
Sivalingam, S.
Schenk, L. M.
Koller, A. C.
Fischer, S. B.
Thiele, H.
Nuernberg, P.
Guzman Parra, J.
Orozco Diaz, G.
Auburger, G.
Albus, M.
Borrmann-Hassenbach, M.
Jose Gonzalez, M.
Gil Flores, S.
Cabaleiro Fabeiro, F. J.
del Rio Noriega, F.
Perez Perez, F.
Haro Gonzalez, J.
Rivas, F.
Mayoral, F.
Herms, S.
Hoffmann, P.
Cichon, S.
Rietschel, M.
Noethen, M. M.
Forstner, A. J.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 261 - 262
[3] WHOLE EXOME SEQUENCING OF MULTIPLEX BIPOLAR DISORDER FAMILIES AND FOLLOW-UP RESEQUENCING IMPLICATE RARE VARIANTS IN CELL ADHESION GENES CONTRIBUTING TO DISEASE ETIOLOGY
Maaser, Anna
Streit, Fabian
Ludwig, Kerstin U.
Koller, Anna C.
Degenhardt, Franziska
Thiele, Holger
Parra, Jose Guzman
Rivas, Fabio
Mayoral, Fermin
Herms, Stefan
Hoffmann, Per
Cichon, Sven
Rietschel, Marcella
Noethen, Markus M.
Forstner, Andreas J.
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : 1088 - 1089
[4] Exome Sequencing of 75 Individuals from Multiply Affected Coeliac Families and Large Scale Resequencing Follow Up
Mistry, Vanisha
Bockett, Nicholas A.
Levine, Adam P.
Mirza, Muddassar M.
Hunt, Karen A.
Ciclitira, Paul J.
Hummerich, Holger
Neuhausen, Susan L.
Simpson, Michael A.
Plagnol, Vincent
van Heel, David A.
PLOS ONE, 2015, 10 (01):
[5] Identification of rare risk variants in 12 multiply affected families with bipolar disorder
Vettiger, A.
Fischer, S.
Herms, S.
Hoffmann, P.
Cichon, S.
Maaser, A.
Streit, F.
Witt, S. H.
Guzman-Parra, J.
Orozco-Diaz, G.
Auburger, G.
Albus, M.
Borrmann-Hassenbach, M.
Gonzalez, M.
Gil-Flores, S.
Cabaleiro-Fabeiro, F.
Noriega, F. Del Rio
Perez-Perez, F.
Haro-Gonzalez, J.
Rivas, F.
Mayoral, F.
Rietschel, M.
Noethen, M.
Foerstner, P.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 379 - 379
[6] FOLLOW-UP OF 27 CANDIDATE GENES FROM A WHOLE-EXOME SEQUENCING STUDY IN LARGE FAMILIES WITH BIPOLAR DISORDER BY RESEQUENCING OF AN INDEPENDENT PATIENT-CONTROL COHORT
Fischer, Sascha
Hoffmann, Per
Reinbold, Celine
Burger, Bettina
Herms, Stefan
Streit, Fabian
Rivas, Fabio
Mayoral, Fermin
Parra, Jose Guzman
Arias, Barbara
Schulze, Thomas
Rietschel, Marcella
Noethen, Markus
Forstner, Andreas
Cichon, Sven
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2021, 51 : E62 - E63
[7] Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families
Andreas J. Forstner
Sascha B. Fischer
Lorena M. Schenk
Jana Strohmaier
Anna Maaser-Hecker
Céline S. Reinbold
Sugirthan Sivalingam
Julian Hecker
Fabian Streit
Franziska Degenhardt
Stephanie H. Witt
Johannes Schumacher
Holger Thiele
Peter Nürnberg
José Guzman-Parra
Guillermo Orozco Diaz
Georg Auburger
Margot Albus
Margitta Borrmann-Hassenbach
Maria José González
Susana Gil Flores
Francisco J. Cabaleiro Fabeiro
Francisco del Río Noriega
Fermin Perez Perez
Jesus Haro González
Fabio Rivas
Fermin Mayoral
Michael Bauer
Andrea Pfennig
Andreas Reif
Stefan Herms
Per Hoffmann
Mehdi Pirooznia
Fernando S. Goes
Marcella Rietschel
Markus M. Nöthen
Sven Cichon
Translational Psychiatry, 10
[8] Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families
Forstner, Andreas J.
Fischer, Sascha B.
Schenk, Lorena M.
Strohmaier, Jana
Maaser-Hecker, Anna
Reinbold, Celine S.
Sivalingam, Sugirthan
Hecker, Julian
Streit, Fabian
Degenhardt, Franziska
Witt, Stephanie H.
Schumacher, Johannes
Thiele, Holger
Nuernberg, Peter
Guzman-Parra, Jose
Orozco Diaz, Guillermo
Auburger, Georg
Albus, Margot
Borrmann-Hassenbach, Margitta
Jose Gonzalez, Maria
Gil Flores, Susana
Cabaleiro Fabeiro, Francisco J.
del Rio Noriega, Francisco
Perez Perez, Fermin
Haro Gonzalez, Jesus
Rivas, Fabio
Mayoral, Fermin
Bauer, Michael
Pfennig, Andrea
Reif, Andreas
Herms, Stefan
Hoffmann, Per
Pirooznia, Mehdi
Goes, Fernando S.
Rietschel, Marcella
Noethen, Markus M.
Cichon, Sven
TRANSLATIONAL PSYCHIATRY, 2020, 10 (01)
[9] WHOLE GENOME SEQUENCING APPROACH TO IDENTIFY SUSCEPTIBILITY RARE VARIANTS IN A MULTIPLEX NUCLEAR FAMILY OF SCHIZOPHRENIA AND FOLLOW-UP RESEQUENCING
Yu, Shun-Chun
Chen, Hsuan-Yu
Yu, Sung-Liang
Liu, Chih-Min
Hwu, Hai-Gwo
Chen, Wei J.
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : S1011 - S1012
[10] Novel Rare Missense Variations and Risk of Autism Spectrum Disorder: Whole-Exome Sequencing in Two Families with Affected Siblings and a Two-Stage Follow-Up Study in a Japanese Population
Egawa, Jun
Watanabe, Yuichiro
Wang, Chenyao
Inoue, Emiko
Sugimoto, Atsunori
Sugiyama, Toshiro
Igeta, Hirofumi
Nunokawa, Ayako
Shibuya, Masako
Kushima, Itaru
Orime, Naoki
Hayashi, Taketsugu
Okada, Takashi
Uno, Yota
Ozaki, Norio
Someya, Toshiyuki
PLOS ONE, 2015, 10 (03):

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