Scientific Publications

Reponse to De Leeuw and Houge

A.K. Arndt
C.A. Macrae
S. Klaassen

Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients

S. Sasse-Klaassen
B. Gerull
E. Oechslin
R. Jenni
L. Thierfelder

Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15

S. Sasse-Klaassen
S. Probst
B. Gerull
E. Oechslin
P. Nuernberg
A. Heuser
R. Jenni
H.C. Hennies
L. Thierfelder

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

B. Gerull
A. Heuser
T. Wichter
M. Paul
C.T. Basson
D.A. McDermott
B.B. Lerman
S.M. Markowitz
P.T. Ellinor
C.A. MacRae
S. Peters
K.S. Grossmann
J. Drenckhahn
B. Michely
S. Sasse-Klaassen
W. Birchmeier
R. Dietz
G. Breithardt
E. Schulze-Bahr
L. Thierfelder

Response to correspondence by Dr. Finsterer and Dr. Stoellberger: Heterogenous myopathic background of left ventricular hypertrabeculation/noncompaction

L. Thierfelder
S. Sasse-Klaassen
B. Gerull
R. Jenni
E. Oechslin

Lack of association of the G protein-coupled receptor for asthma susceptibility gene with atopic dermatitis

C. Soederhaell
I. Marenholz
R. Nickel
C. Grueber
R. Kehrt
K. Rohde
R.W. Griffioen
P. Meglio
L. Tarani
D. Gustafsson
U. Hoffmann
B. Gerstner
S. Mueller
U. Wahn
Y.A. Lee

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

B. Gerull
M. Gramlich
J. Atherton
M. McNabb
K. Trombitas
S. Sasse-Klaassen
J.G. Seidman
C. Seidman
H. Granzier
S. Labeit
M. Frenneaux
L. Thierfelder

SARS-CoV-2 infection dynamics revealed by wastewater sequencing analysis and deconvolution

V.F. Schumann
R.R. de Castro Cuadrat
E. Wyler
R. Wurmus
A. Deter
C. Quedenau
J. Dohmen
M. Faxel
T. Borodina
A. Blume
J. Freimuth
M. Meixner
J.H. Grau
K. Liere
T. Hackenbeck
F. Zietzschmann
R. Gnirss
U. Böckelmann
B. Uyar
V. Franke
N. Barke
J. Altmüller
N. Rajewsky
M. Landthaler
A. Akalin

An interdisciplinary approach to characterize peanut-allergic patients - first data from the FOOD@ consortium

M. Worm
A. Alexiou
V. Höfer
T. Birkner
A.C.S.N. Jeanrenaud
F. Fauchère
K. Pazur
C. Steinert
A. Arnau-Soler
P. Banerjee
A. Diefenbach
J. Dobbertin-Welsch
S. Dölle-Bierke
W. Francuzik
A. Ghauri
S. Heller
B. Kalb
U. Löber
I. Marenholz
L. Markó
J. Scheffel
O. Potapenko
St. Roll
S. Lau
Y.A. Lee
J. Braun
A. Thiel
M. Babina
S. Altrichter
S.K. Forslund
K. Beyer

July 29, 2021 / PLoS Genet

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

E. Audain
A. Wilsdon
J. Breckpot
J.M. Izarzugaza
T.W. Fitzgerald
A.K. Kahlert
A. Sifrim
F. Wünnemann
Y. Perez-Riverol
H. Abdul-Khaliq
M. Bak
A.S. Bassett
W.D. Benson
F. Berger
I. Daehnert
K. Devriendt
S. Dittrich
P.E. Daubeney
V. Garg
K. Hackmann
K. Hoff
P. Hofmann
G. Dombrowsky
T. Pickardt
U. Bauer
B.D. Keavney
S. Klaassen
H.H. Kramer
C.R. Marshall
D.M. Milewicz
S. Lemaire
J.S. Coselli
M.E. Mitchell
A. Tomita-Mitchell
S.K. Prakash
K. Stamm
A.F.R. Stewart
C.K. Silversides
R. Siebert
B. Stiller
J.A. Rosenfeld
I. Vater
A.V. Postma
A. Caliebe
J.D. Brook
G. Andelfinger
M.E. Hurles
B. Thienpont
L.A. Larsen
M.P. Hitz