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1

Sex, Violence, and the Avant-Garde: Anarchism in Interwar France

Windpassinger, Gwendolyn

Journal:

Journal of Contemporary European Studies

Année:

2011

Langue:

english

Fichier:

PDF, 63 KB

english, 2011

2

Towards Enhancement of Early-Stage Chilling Tolerance and Root Development in Sorghum F1 Hybrids

Windpassinger, S., Friedt, W., Deppé, I., Werner, C., Snowdon, R., Wittkop, B.

Journal:

Journal of Agronomy and Crop Science

Année:

2016

Langue:

english

Fichier:

PDF, 364 KB

english, 2016

3

Women in Executive Power: A Global Overview

Windpassinger, Gwendolyn

Journal:

Journal of Contemporary European Studies

Année:

2012

Langue:

english

Fichier:

PDF, 66 KB

english, 2012

4

Candidate region for Gilles de la Tourette syndrome at 7q31

Peter M. Kroisel, Erwin Petek, Werner Emberger, Christian Windpassinger, Wolfgang Wladika, Klaus Wagner

Journal:

American Journal of Medical Genetics Part A

Année:

2001

Langue:

english

Fichier:

PDF, 67 KB

english, 2001

5

De novo translocation t(5;18)(q33.1;q12.1) associated with autistic disorder

Peter M. Kroisel, Christian Windpassinger, Klaus Wagner, Erwin Petek, John B. Vincent, Stephen W. Scherer, Georg Spiel, Vida Artner, Erich Valtiner

Journal:

American Journal of Medical Genetics Part A

Année:

2004

Langue:

english

Fichier:

PDF, 104 KB

english, 2004

6

Tunable Gauge Potential for Neutral and Spinless Particles in Driven Optical Lattices

Struck, J., Ölschläger, C., Weinberg, M., Hauke, P., Simonet, J., Eckardt, A., Lewenstein, M., Sengstock, K., Windpassinger, P.

Journal:

Physical Review Letters

Année:

2012

Langue:

english

Fichier:

PDF, 577 KB

english, 2012

7

[IEEE GLOBECOM '03. IEEE Global Telecommunications Conference - San Francisco, CA, USA (1-5 Dec. 2003)] GLOBECOM '03. IEEE Global Telecommunications Conference (IEEE Cat. No.03CH37489) - Improved MIMO precoding for decentralized receivers resembling concepts from lattice reduction

Fischer, R.F.H., Windpassinger, C.A.

Année:

2003

Langue:

english

Fichier:

PDF, 289 KB

english, 2003

8

Feynmans Idee wird Realität

Windpassinger, Patrick

Journal:

Physik in unserer Zeit

Année:

2014

Langue:

german

Fichier:

PDF, 948 KB

german, 2014

9

Queering anarchism in post-2001 Buenos Aires

Windpassinger, G.

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 134 KB

english, 2010

10

Anarchism and sexuality

Windpassinger, Gwendolyn, Cleminson, Richard

Journal:

International Journal of Iberian Studies

Année:

2012

Langue:

english

Fichier:

PDF, 328 KB

english, 2012

11

Three different profiles: Early socio-communicative capacities in typical Rett syndrome, the preserved speech variant and normal development

Marschik, Peter B., Bartl-Pokorny, Katrin D., Tager-Flusberg, Helen, Kaufmann, Walter E., Pokorny, Florian, Grossmann, Tobias, Windpassinger, Christian, Petek, Erwin, Einspieler, Christa

Journal:

Developmental Neurorehabilitation

Année:

2014

Langue:

english

Fichier:

PDF, 217 KB

english, 2014

12

A compact and robust diode laser system for atom interferometry on a sounding rocket

Schkolnik, V., Hellmig, O., Wenzlawski, A., Grosse, J., Kohfeldt, A., Döringshoff, K., Wicht, A., Windpassinger, P., Sengstock, K., Braxmaier, C., Krutzik, M., Peters, A.

Journal:

Applied Physics B: Lasers and Optics

Année:

2016

Langue:

english

Fichier:

PDF, 1.24 MB

english, 2016

13

Opioid use after propofol or sevoflurane anesthesia: a randomized trial

Windpassinger, Marita, Plattner, Olga, Gemeiner, Jana, Böhler, Kornelia, Luntzer, Robert, Klimscha, Walter, Yang, Dongsheng, Mascha, Edward J., Sessler, Daniel I.

Journal:

Canadian Journal of Anesthesia/Journal canadien d'anesthésie

Année:

2016

Fichier:

PDF, 623 KB

2016

14

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

Harripaul, R, Vasli, N, Mikhailov, A, Rafiq, M A, Mittal, K, Windpassinger, C, Sheikh, T I, Noor, A, Mahmood, H, Downey, S, Johnson, M, Vleuten, K, Bell, L, Ilyas, M, Khan, F S, Khan, V, Moradi, M, Ay

Journal:

Molecular Psychiatry

Année:

2017

Langue:

english

Fichier:

PDF, 2.77 MB

english, 2017

15

[IEEE 2017 Conference on Lasers and Electro-Optics Pacific Rim (CLEO-PR) - Singapore, Singapore (2017.7.31-2017.8.4)] 2017 Conference on Lasers and Electro-Optics Pacific Rim (CLEO-PR) - Design of a compact diode laser system for dual-species atom interferometry with rubidium and potassium in space

Anton, Oliver, Doringshoff, Klaus, Schkolnik, Vladimir, Kanthak, Simon, Kurbis, Christian, Grose, Jens, Elsen, Michael, Wenzlawski, Andre, Mihm, Moritz, Windpassinger, Patrick, Krutzik, Markus, Peters

Année:

2017

Langue:

english

Fichier:

PDF, 2.90 MB

english, 2017

16

Systematic optimization of laser cooling of dysprosium

Mühlbauer, Florian, Petersen, Niels, Baumgärtner, Carina, Maske, Lena, Windpassinger, Patrick

Journal:

Applied Physics B Photophysics and Laser Chemistry

Année:

2018

Langue:

english

Fichier:

PDF, 1.52 MB

english, 2018

17

Micro-lensing-induced line shapes in a single-mode cold-atom–hollow-core-fiber interface

Noaman, Mohammad, Langbecker, Maria, Windpassinger, Patrick

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 1.56 MB

english, 2018

18

Spectroscopy of the 1001-nm transition in atomic dysprosium

Petersen, N., TrÃ¼mper, M., Windpassinger, P.

Journal:

Physical Review A

Année:

2020

Fichier:

PDF, 433 KB

2020

19

Effect of Ketamine on Limbic GABA and Glutamate: A Human In Vivo Multivoxel Magnetic Resonance Spectroscopy Study

Silberbauer, Leo R., Spurny, Benjamin, Handschuh, Patricia, KlÃ¶bl, Manfred, Bednarik, Petr, Reiter, Birgit, Ritter, Vera, Trost, Patricia, Konadu, Melisande E., Windpassinger, Marita, Stimpfl, Thomas

Journal:

Frontiers in Psychiatry

Année:

2020

Fichier:

PDF, 1.22 MB

2020

20

Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: Confirmation and refinement of the DFNA25 locus

Erwin Petek, Christian Windpassinger, Monika Mach, Ludwig Rauter, Stephen W. Scherer, Klaus Wagner, Peter M. Kroisel

Journal:

American Journal of Medical Genetics Part A

Année:

2003

Langue:

english

Fichier:

PDF, 155 KB

english, 2003

21

A new 3p interstitial deletion including the entire MITF gene causes a variation of Tietz/Waardenburg type IIA syndromes

Thomas Schwarzbraun, Lisa Ofner, Gabriele Gillessen-Kaesbach, Barbara Schaperdoth, Karl-Heinz Preisegger, Christian Windpassinger, Klaus Wagner, Erwin Petek, Peter M. Kroisel

Journal:

American Journal of Medical Genetics Part A

Année:

2007

Langue:

english

Fichier:

PDF, 224 KB

english, 2007

22

Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q

John B. Vincent, Abdul Noor, Christian Windpassinger, Peter J. Gianakopoulos, Thomas Schwarzbraun, Simon E. Alfred, Beata Stachowiak, Stephen W. Scherer, Wendy Roberts, Klaus Wagner, Peter M. Kroisel,

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 359 KB

english, 2009

23

Mutations in MECP2 exon 1 in classical rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2

Peter J. Gianakopoulos, Yuzhi Zhang, Nela Pencea, Marija Orlic-Milacic, Kirti Mittal, Christian Windpassinger, Sara-Jane White, Peter M. Kroisel, Eva W.C. Chow, Carol J. Saunders, Berge A. Minassian,

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 239 KB

english, 2012

24

Lattice-reduction-aided MMSE equalization and the successive estimation of correlated data

Robert F.H. Fischer, Christoph Windpassinger, Clemens Stierstorfer, Christian Siegl, Andreas Schenk, Ümit Abay

Journal:

AEU - International Journal of Electronics and Communications

Année:

2011

Langue:

english

Fichier:

PDF, 304 KB

english, 2011

25

Signal processing in decision-feedback equalization of intersymbol-interference and multiple-input/multiple-output channels: a unified view

Robert Fischer, Johannes Huber, Christoph Windpassinger

Journal:

Signal Processing

Année:

2003

Langue:

english

Fichier:

PDF, 270 KB

english, 2003

26

Molecular characterization of a unique de novo 15q deletion associated with Prader–Willi syndrome and central visual impairment

C Windpassinger, E Petek, K Wagner, A Langmann, K Buiting, PM Kroisel

Journal:

Clinical Genetics

Année:

2003

Langue:

english

Fichier:

PDF, 2.93 MB

english, 2003

27

IT-Outsourcing - Gesundheitsreform oder Rosskur für Banken?

Carmen Koberstein-Windpassinger

Journal:

Année:

2004

Langue:

german

Fichier:

PDF, 97 KB

german, 2004

28

Alles ist Zahl

Gerhard Stahl, Carmen Koberstein-Windpassinger

Journal:

Année:

2005

Langue:

german

Fichier:

PDF, 79 KB

german, 2005

29

SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease

Carina Fischer, Slave Trajanoski, Lea Papić, Christian Windpassinger, Günther Bernert, Michael Freilinger, Maria Schabhüttl, Mine Arslan-Kirchner, Poupak Javaher-Haghighi, Barbara Plecko, Jan Senderek

Journal:

Journal of Neurology

Année:

2012

Langue:

english

Fichier:

PDF, 593 KB

english, 2012

30

Molecular and genomic studies ofIMMP2Land mutation screening in autism and Tourette syndrome

Erwin Petek, Thomas Schwarzbraun, Abdul Noor, Megha Patel, Kazuhiko Nakabayashi, Sanaa Choufani, Christian Windpassinger, Mara Stamenkovic, Mary M. Robertson, Harald N. Aschauer, Hugh M. D. Gurling, P

Journal:

Molecular Genetics and Genomics

Année:

2007

Langue:

english

Fichier:

PDF, 469 KB

english, 2007

31

Refinement of the "Silver syndrome locus" on chromosome 11q12-q14 in four families and exclusion of eight candidate genes

Christian Windpassinger, Klaus Wagner, Erwin Petek, Renate Fischer, Michaela Auer-Grumbach

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 301 KB

english, 2003

32

Molecular characterisation of a 15

Erwin Petek, Christian Windpassinger, Burkhard Simma, Thomas Mueller, Klaus Wagner, Peter M. Kroisel

Journal:

Journal of Human Genetics

Année:

2003

Langue:

english

Fichier:

PDF, 268 KB

english, 2003

33

Phenotypic and molecular characterisation of a de novo 5q deletion that includes theAPCgene

Lisa Ofner, Jochen Raedle, Christian Windpassinger, Thomas Schwarzbraun, Peter M. Kroisel, Klaus Wagner, Erwin Petek

Journal:

Journal of Human Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 306 KB

english, 2006

34

Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations

Miltenberger-Miltenyi, Gabriel, Schwarzbraun, Thomas, Löscher, Wolfgang N, Wanschitz, Julia, Windpassinger, Christian, Duba, Hans-Christoph, Seidl, Rainer, Albrecht, Gerhard, Weirich-Schwaiger, Helga,

Journal:

European Journal of Human Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 373 KB

english, 2009

35

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

Windpassinger, Christian, Auer-Grumbach, Michaela, Irobi, Joy, Patel, Heema, Petek, Erwin, Hörl, Gerd, Malli, Roland, Reed, Johanna A, Dierick, Ines, Verpoorten, Nathalie

Journal:

Nature Genetics

Année:

2004

Langue:

english

Fichier:

PDF, 1.36 MB

english, 2004

36

Multi-component quantum gases in spin-dependent hexagonal lattices

Soltan-Panahi, P., Struck, J., Hauke, P., Bick, A., Plenkers, W., Meineke, G., Becker, C., Windpassinger, P., Lewenstein, M., Sengstock, K.

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 1.63 MB

english, 2011

37

Echo spectroscopy of atomic dynamics in a Gaussian trap via phase imprints

D. Oblak, J. Appel, P. J. Windpassinger, U. B. Hoff, N. Kjærgaard, E. S. Polzik

Journal:

The European Physical Journal D / Atomic, Molecular, Optical and Plasma Physics

Année:

2008

Langue:

english

Fichier:

PDF, 535 KB

english, 2008

38

CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa

Abdul Noor, Christian Windpassinger, Megha Patel, Beata Stachowiak, Anna Mikhailov, Matloob Azam, Muhammad Irfan, Zahid Kamal Siddiqui, Farooq Naeem, Andrew D. Paterson, Muhammad Lutfullah, John B. Vi

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 1.21 MB

english, 2008

39

CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa

Abdul Noor, Christian Windpassinger, Megha Patel, Beata Stachowiak, Anna Mikhailov, Matloob Azam, Muhammad Irfan, Andrew D. Paterson, Muhammad Lutufullah, Dan Doherty, John B. Vincent, Muhammad Ayub

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 32 KB

english, 2008

40

Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3

Abdul Noor, Christian Windpassinger, Irina Vitcu, Marija Orlic, Muhammad Arshad Rafiq, Mahwish Khalid, Mahmood Nasir Malik, Muhammad Ayub, Benjamin Alman, John B. Vincent

Journal:

The American Journal of Human Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 521 KB

english, 2009

41

Lattice-reduction-aided broadcast precoding

Windpassinger, C., Fischer, R.F.H., Huber, J.B.

Journal:

IEEE Transactions on Communications

Année:

2004

Langue:

english

Fichier:

PDF, 259 KB

english, 2004

42

Multiple-symbol differential sphere decoding

Lampe, L., Schober, R., Pauli, V., Windpassinger, C.

Journal:

IEEE Transactions on Communications

Année:

2005

Langue:

english

Fichier:

PDF, 289 KB

english, 2005

43

Precoding in multiantenna and multiuser communications

Windpassinger, C., Fischer, R.F.H., Vencel, T., Huber, J.B.

Journal:

IEEE Transactions on Wireless Communications

Année:

2004

Langue:

english

Fichier:

PDF, 497 KB

english, 2004

44

Clinical and Electrophysiological Features in Charcot-Marie-Tooth Disease With Mutations in the NEFL Gene

Windpassinger, C., Auer-Grumbach, M., Loscher, W. N., Miltenberger-Miltenyi, G., Janecke, A. R., Wanschitz, J. V., Timmerman, V.

Journal:

Archives of Neurology

Année:

2007

Langue:

english

Fichier:

PDF, 127 KB

english, 2007

45

Quantum Simulation of Frustrated Classical Magnetism in Triangular Optical Lattices

Struck, J., Olschlager, C., Le Targat, R., Soltan-Panahi, P., Eckardt, A., Lewenstein, M., Windpassinger, P., Sengstock, K.

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 552 KB

english, 2011

46

An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1

Christian Windpassinger, Benedikt Schoser, Volker Straub, Sonja Hochmeister, Abdul Noor, Birgit Lohberger, Natalie Farra, Erwin Petek, Thomas Schwarzbraun, Lisa Ofner, Wolfgang N. Löscher, Klaus Wagne

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 1.29 MB

english, 2008

47

Thin corpus callosum and amyotrophy in spastic paraplegia—Case report and review of literature

Beate Winner, Claudia Gross, Gökhan Uyanik, Wilhelm Schulte-Mattler, Ralf Lürding, Jörg Marienhagen, Ulrich Bogdahn, Christian Windpassinger, Ute Hehr, Jürgen Winkler

Journal:

Clinical Neurology and Neurosurgery

Année:

2006

Langue:

english

Fichier:

PDF, 287 KB

english, 2006

48

Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS)

Thomas Schwarzbraun, Christian Windpassinger, Lisa Ofner, John B. Vincent, Joseph Cheung, Stephen W. Scherer, Klaus Wagner, Peter M. Kroisel, Erwin Petek

Journal:

European Journal of Medical Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 552 KB

english, 2006

49

Membrane topology of the human seipin protein

Carolina Lundin, Rickard Nordström, Klaus Wagner, Christian Windpassinger, Helena Andersson, Gunnar von Heijne, IngMarie Nilsson

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 164 KB

english, 2006

50

G.P.14.13 Phenotypic characterization of two unrelated UK families with X-linked myopathy and an identical mutation in the FHL1 gene

A. Sarkozy, K. Bushby, D. Hilton-Jones, C.F. Dougan, H. Lochmüller, C. Windpassinger, V. Straub

Journal:

Neuromuscular Disorders

Année:

2008

Langue:

english

Fichier:

PDF, 50 KB

english, 2008