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1

The Ethics of Gamification in a Marketing Context

Thorpe, Andrea Stevenson, Roper, Stephen

Journal:

Journal of Business Ethics

Year:

2017

Language:

english

File:

PDF, 529 KB

english, 2017

2

Individual Radiosensitivity Measured With Lymphocytes May Predict the Risk of Acute Reaction After Radiotherapy

Kerstin Borgmann, Ulrike Hoeller, Sven Nowack, Michael Bernhard, Barbara Röper, Sophie Brackrock, Cordula Petersen, Silke Szymczak, Andreas Ziegler, Petra Feyer, Winfried Alberti, Ekkehard Dikomey

Journal:

International Journal of Radiation Oncology*Biology*Physics

Year:

2008

Language:

english

File:

PDF, 291 KB

english, 2008

3

Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathies

Andrea Klein, Suzanne Lillis, Iulia Munteanu, Mariacristina Scoto, Haiyan Zhou, Ros Quinlivan, Volker Straub, Adnan Y. Manzur, Helen Roper, Pierre-Yves Jeannet, Wojtek Rakowicz, David Hilton Jones, Uf

Journal:

Year:

2012

Language:

english

File:

PDF, 326 KB

english, 2012

4

Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia–Parkinsonism (DYT3)

Andrea H. Németh, Dagmar Nolte, Eimear Dunne, Stephan Niemann, Markus Kostrzewa, Usha Peters, Eileen Fraser, Elena Bochukova, Robin Butler, Julie Brown, Roger D. Cox, Elaine R. Levy, Hans-Hilger Roper

Journal:

Year:

1999

Language:

english

File:

PDF, 156 KB

english, 1999

5

Knowledge, Capabilities and Manufacturing Innovation: A USA–Europe Comparison

Roper, Stephen, Youtie, Jan, Shapira, Philip, Fernández-Ribas, Andrea

Journal:

Regional Studies

Year:

2010

Language:

english

File:

PDF, 321 KB

english, 2010

6

Terrain‐aided navigation for long‐endurance and deep‐rated autonomous underwater vehicles

Salavasidis, Georgios, Munafò, Andrea, Harris, Catherine A., Prampart, Thomas, Templeton, Robert, Smart, Micheal, Roper, Daniel T., Pebody, Miles, McPhail, Stephen D., Rogers, Eric, Phillips, Alexande

Journal:

Journal of Field Robotics

Year:

2018

Language:

english

File:

PDF, 11.69 MB

english, 2018

7

Cosegregation of T108A Elk-1 with mental retardation

Andreas Schröer, Maurice P. Scheer, Sylvia Zacharias, Silke Schneider, Hans Hilger Ropers, Hans Gerd Nothwang, Jamel Chelly, Ben Hamel, Jean-Pierre Fryns, Peter Shaw, Claude Moraine

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 99 KB

english, 2000

8

Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences

Andreas Tzschach, Ines Krause-Plonka, Corinna Menzel, Vera Kalscheuer, Holger Toennies, Harry Scherthan, Andreas Knoblauch, Michael Radke, Hans-Hilger Ropers, Maria Hoeltzenbein

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 181 KB

english, 2006

9

Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion

Andreas Tzschach, Ines Krause-Plonka, Corinna Menzel, Andreas Knoblauch, Holger Toennies, Maria Hoeltzenbein, Michael Radke, Hans-Hilger Ropers, Vera Kalscheuer

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 104 KB

english, 2006

10

Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH

Andreas Tzschach, Corinna Menzel, Fikret Erdogan, Marei Schubert, Maria Hoeltzenbein, Gotthold Barbi, Christine Petzenhauser, Hans-Hilger Ropers, Reinhard Ullmann, Vera Kalscheuer

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 149 KB

english, 2007

11

Characterization of interstitial Xp duplications in two families by tiling path array CGH

Andreas Tzschach, Wei Chen, Fikret Erdogan, Adelheid Hoeller, Hans-Hilger Ropers, Claudio Castellan, Reinhard Ullmann, Albert Schinzel

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 241 KB

english, 2008

12

Chromosome deletions in 13q33–34: Report of four patients and review of the literature

Joanna Walczak-Sztulpa, Marzena Wisniewska, Anna Latos-Bielenska, Maja Linné, Christina Kelbova, Britta Belitz, Lutz Pfeiffer, Vera Kalscheuer, Fikret Erdogan, Andreas W. Kuss, Hans-Hilger Ropers, Rei

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 166 KB

english, 2008

13

Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis

Ariana Kariminejad, Roxana Kariminejad, Andreas Tzschach, Reinhard Ullmann, Alisho Ahmed, Alaleh Asghari-Roodsari, Shadab Salehpour, Fariba Afroozan, Hans-Hilger Ropers, Mohammad Hasan Kariminejad

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 136 KB

english, 2009

14

Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement

Andreas Tzschach, Corinna Menzel, Fikret Erdogan, Erman Salih Istifli, Martin Rieger, Angela Ovens-Raeder, Alfons Macke, Hans-Hilger Ropers, Reinhard Ullmann, Vera Kalscheuer

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 138 KB

english, 2010

15

11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features

Ariana Kariminejad, Roxana Kariminejad, Andreas Tzschach, Hamid Najafi, Alischo Ahmed, Reinhard Ullmann, Hans-Hilger Ropers, Mohamad Hasan Kariminejad

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 121 KB

english, 2010

16

A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian family

Masoud Garshasbi, Kimia Kahrizi, Masoumeh Hosseini, Leila Nouri Vahid, Masoumeh Falah, Sahel Hemmati, Hao Hu, Andreas Tzschach, Hans Hilger Ropers, Hossein Najmabadi, Andreas Walter Kuss

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 2.05 MB

english, 2011

17

Novel GDI1 mutation in a large family with nonsyndromic X-linked intellectual disability

Gertrud Strobl-Wildemann, Vera M. Kalscheuer, Hao Hu, Klaus Wrogemann, Hans-Hilger Ropers, Andreas Tzschach

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 951 KB

english, 2011

18

Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis

Alexander Herr, Dominique Meunier, Ines Müller, Andreas Rump, Reinald Fundele, H.-Hilger Ropers, Ulrike A. Nuber

Journal:

Developmental Dynamics

Year:

2003

Language:

english

File:

PDF, 963 KB

english, 2003

19

Novel JARID1C/SMCX mutations in patients with X-linked mental retardation

Andreas Tzschach, Steffen Lenzner, Bettina Moser, Richard Reinhardt, Jamel Chelly, Jean-Pierre Fryns, Tjitske Kleefstra, Martine Raynaud, Gillian Turner, Hans-Hilger Ropers, Andreas Kuss, Lars Riff Je

Journal:

Year:

2006

Language:

english

File:

PDF, 172 KB

english, 2006

20

Luminescence studies of interacting metal complexes in two dimensions

Howard H. Patterson, Gerald Roper, John Biscoe, Andreas Ludi, Nils Blom

Journal:

Journal of Luminescence

Year:

1984

Language:

english

File:

PDF, 136 KB

english, 1984

21

Social networks and getting a home: Do contacts matter?

Andrea Röper, Beate Völker, Henk Flap

Journal:

Social Networks

Year:

2009

Language:

english

File:

PDF, 267 KB

english, 2009

22

X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome

Ursula Friedrich, Mette Warburg, Peter Wieacker, Thomas F. Wienker, Andreas Gal, Hans-Hilger Ropers

Journal:

Year:

1985

Language:

english

File:

PDF, 543 KB

english, 1985

23

Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literature

Yousef Shafeghati, Kimia Kahrizi, Hossein Najmabadi, Andreas Walter Kuss, Hans-Hilger Ropers, Andreas Tzschach

Journal:

European Journal of Pediatrics

Year:

2010

Language:

english

File:

PDF, 206 KB

english, 2010

24

Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

Hao Hu, Klaus Wrogemann, Vera Kalscheuer, Andreas Tzschach, Hugues Richard, Stefan A. Haas, Corinna Menzel, Melanie Bienek, Guy Froyen, Martine Raynaud, Hans Van Bokhoven, Jamel Chelly, Hilger Ropers,

Journal:

The HUGO Journal

Year:

2009

Language:

english

File:

PDF, 349 KB

english, 2009

25

Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

Hao Hu, Klaus Wrogemann, Vera Kalscheuer, Andreas Tzschach, Hugues Richard, Stefan A. Haas, Corinna Menzel, Melanie Bienek, Guy Froyen, Martine Raynaud, Hans Van Bokhoven, Jamel Chelly, Hilger Ropers,

Journal:

The HUGO Journal

Year:

2009

Language:

english

File:

PDF, 88 KB

english, 2009

26

Comparison of Telephone with World Wide Web-Based Responses by Parents and Teens to a Follow-Up Survey after Injury

Frederick P. Rivara, Thomas D. Koepsell, Jin Wang, Dennis Durbin, Kenneth M. Jaffe, Monica Vavilala, Andrea Dorsch, Maria Roper-Caldbeck, Eileen Houseknecht, Nancy Temkin

Journal:

Health Services Research

Year:

2011

Language:

english

File:

PDF, 191 KB

english, 2011

27

An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4

Kahrizi, Kimia, Najmabadi, Hossein, Kariminejad, Roxana, Jamali, Payman, Malekpour, Mahdi, Garshasbi, Masoud, Ropers, Hans Hilger, Kuss, Andreas Walter, Tzschach, Andreas

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 178 KB

english, 2008

28

Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11

Tzschach, Andreas, Bisgaard, Anne-Marie, Kirchhoff, Maria, Graul-Neumann, Luitgard M, Neitzel, Heidemarie, Page, Stephanie, Ahmed, Alischo, Müller, Ines, Erdogan, Fikret, Ropers, Hans-Hilger

Journal:

European Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 400 KB

english, 2009

29

Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3

Hu, Cougar Hao, Garshasbi, Masoud, Abedini, Seyedeh Sedigheh, Ghadami, Shirin, Kariminejad, Roxana, Ullmann, Reinhard, Chen, Wei, Ropers, H-Hilger, Kuss, Andreas W, Kahrizi, Kimia

Journal:

European Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 230 KB

english, 2010

30

Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3

Tzschach, Andreas, Hoeltzenbein, Maria, Hoffmann, Kirsten, Menzel, Corinna, Beyer, Alexander, Ocker, Volker, Wurster, Goetz, Raynaud, Martine, Ropers, Hans-Hilger, Kalscheuer, Vera

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 99 KB

english, 2006

31

Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation

Chen, Wei, Jensen, Lars R, Gecz, Jozef, Fryns, Jean-Pierre, Moraine, Claude, de Brouwer, Arjan, Chelly, Jamel, Moser, Bettina, Ropers, H Hilger, Kuss, Andreas W

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 97 KB

english, 2006

32

Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome

Moheb, Lia Abbasi, Tzschach, Andreas, Garshasbi, Masoud, Kahrizi, Kimia, Darvish, Hossein, Heshmati, Yaser, Kordi, Alireza, Najmabadi, Hossein, Ropers, Hans Hilger, Kuss, Andreas Walter

Journal:

European Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 108 KB

english, 2007

33

Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene associated myopathies

Andrea Klein, Suzanne Lillis, Iulia Munteanu, Mariacristina Scoto, Haiyan Zhou, Ros Quinlivan, Volker Straub, Adnan Y. Manzur, Helen Roper, Pierre-Yves Jeannet, Wojtek Rakowicz, David Hilton Jones, Uf

Journal:

Year:

2012

Language:

english

File:

PDF, 82 KB

english, 2012

34

Einzelbesprechungen

E. Streißler, R. Kerschagl, G. Hedtkamp, C. A. Andreae, A. Montaner, O. Weinberger, A. Nußbaumer, Th. Pütz, B. Röper, St. Wirlandner, A. Graziani, E. März, K. Socher, M. Scheithauer, W. Ehrlicher, H.

Journal:

Journal of Economics

Year:

1960

Language:

german

File:

PDF, 4.61 MB

german, 1960

35

Nome's disease: close linkage with genetic markers from the proximal short arm of the X chromosome

Andreas Gal, Christine Stolzenberger, Thomas Wienker, Peter Wieacker, Hans-Hilger Ropers, Ursula Friedrich, Liesbeth Bleeker-Wagemakers, Peter Pearson, Mette Warburg

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 115 KB

english, 1985

36

Site-Directed Mutagenesis of Conserved Charged Residues in the Helical Region of the Human C5a Receptor : Arg206 Determines High-Affinity Binding Sites of C5a Receptor

Ute Raffetseder, Detlef Röper, Laurence Mery, Claudia Gietz, Andreas Klos, Joachim Grötzinger, Axel Wollmer, François Boulay, Jörg Köhl, Wilfried Bautsch

Journal:

Year:

1996

Language:

english

File:

PDF, 1.36 MB

english, 1996

37

Cloning and Characterization of UXT, a Novel Gene in Human Xp11, which Is Widely and Abundantly Expressed in Tumor Tissue

Andreas Schröer, Silke Schneider, Hans-Hilger Ropers, Hans Gerd Nothwang

Journal:

Year:

1999

Language:

english

File:

PDF, 66 KB

english, 1999

38

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana Kariminejad, Farkhondeh Behjati, Andreas Tzschach, Hossein Najmabadi, Hans Hilger Ropers, Andreas Walter Kuss

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 1.14 MB

english, 2008

39

Cell Flow Reorients the Axis of Planar Polarity in the Wing Epithelium of Drosophila

Benoît Aigouy, Reza Farhadifar, Douglas B. Staple, Andreas Sagner, Jens-Christian Röper, Frank Jülicher, Suzanne Eaton

Journal:

Year:

2010

Language:

english

File:

PDF, 3.51 MB

english, 2010

40

Thromboelastography in patients with acute ischemic stroke

Andrea Elliott, Jeremy Wetzel, Tiffany Roper, Evan Pivalizza, James McCarthy, Cristina Wallace, Mary Jane Hess, Hui Peng, Mohammad H. Rahbar, Navdeep Sangha, James C. Grotta

Journal:

International Journal of Stroke

Year:

2012

Language:

english

File:

PDF, 666 KB

english, 2012

41

Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome “tiling path” BAC array in a girl with heart defect, cleft palate, and developmental delay

Fikret Erdogan, Reinhard Ullmann, Wei Chen, Marei Schubert, Sabine Adolph, Claus Hultschig, Vera Kalscheuer, Hans-Hilger Ropers, Christiane Spaich, Andreas Tzschach

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 202 KB

english, 2007

42

The PERDaix detector

Bachlechner, Andreas, Beischer, Bastian, Greim, Roman, Kirn, Thomas, Mai, Carsten, Yearwood, Gregorio Roper, Schael, Stefan, Schug, David, Tholen, Heiner, Wienkenhöver, Jens

Journal:

Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment

Year:

2012

Language:

english

File:

PDF, 1.08 MB

english, 2012

43

A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family

Püttmann, Lucia, Stehr, Henning, Garshasbi, Masoud, Hu, Hao, Kahrizi, Kimia, Lipkowitz, Bettina, Jamali, Payman, Tzschach, Andreas, Najmabadi, Hossein, Ropers, Hans-Hilger, Musante, Luciana, Kuss, And

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 326 KB

english, 2013

44

A CT-BASED SCORE TO PREDICT THE SUCCESS OF INTERVENTIONAL REVASCULARIZATION OF CHRONIC TOTAL CORONARY OCCLUSIONS

Schuhbaeck, Annika, Lehnhardt, Stephanie, Pflederer, Tobias, Ropers, Dieter, Rixe, Johannes, Schneider, Christian, Rolf, Andreas, Hamm, Christian, Achenbach, Stephan

Journal:

Journal of the American College of Cardiology

Year:

2012

Language:

english

File:

PDF, 90 KB

english, 2012

45

Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome in a Girl with Chromosome Translocation t(2;3)(q33;q23)

Tzschach, Andreas, Kelbova, Christina, Weidensee, Sabine, Peters, Hartmut, Ropers, Hans-Hilger, Ullmann, Reinhard, Erdogan, Fikret, Jurkatis, Jan, Menzel, Corinna, Kalscheuer, Vera, Demuth, Stephanie

Journal:

Ophthalmic Genetics

Year:

2008

Language:

english

File:

PDF, 1.42 MB

english, 2008

46

Optimale Schlaganfallprävention bei geriatrischen Patienten mit Vorhofflimmern

Bahrmann, Philipp, Wehling, Martin, Ropers, Dieter, Flohr, Jürgen, Leischker, Andreas, Röther, Joachim

Journal:

MMW - Fortschritte der Medizin

Year:

2014

Language:

german

File:

PDF, 441 KB

german, 2014

47

Mutations in the candidate gene for Norrie disease

Berger, Wolfgang, de Pol, Dorien van, Warburg, Mette, Gal, Andreas, Bleeker-Wagemakers, Liesbeth, de Silva, Harendra, Meindl, Alfons, Meitinger, Thomas, Cremers, Frans, Ropers, Hans-Hilger

Journal:

Human Molecular Genetics

Year:

1992

Language:

english

File:

PDF, 4.28 MB

english, 1992

48

Safety, Efficacy, and Indications of β-Adrenergic Receptor Blockade to Reduce Heart Rate prior to Coronary CT Angiography 1

Mahabadi, Amir A., Achenbach, Stephan, Burgstahler, Christof, Dill, Thorsten, Fischbach, Roman, Knez, Andreas, Moshage, Werner, Richartz, Barbara M., Ropers, Dieter, Schröder, Stephen, Silber, Sigmund

Journal:

Year:

2010

Language:

english

File:

PDF, 572 KB

english, 2010

49

Schnelle Simulation des TI-TMS320C54x DSP

Pees, Stefan, Hoffmann, Andreas, Ropers, Andreas, Meyr, Heinrich

Journal:

it - Information Technology

Year:

1999

File:

PDF, 612 KB

1999

50

[IEEE 2015 Forum on Specification and Design Languages (FDL) - Barcelona, Spain (2015.9.14-2015.9.16)] 2015 Forum on Specification and Design Languages (FDL) - Virtual hardware-in-the-loop co-simulation for multi-domain automotive systems via the functional mock-up interface

Bucs, Robert Lajos, Murillo, Luis Gabriel, Korotcenko, Ekaterina, Dugge, Gaurav, Leupers, Rainer, Ascheid, Gerd, Ropers, Andreas, Wedler, Markus, Hoffmann, Andreas

Year:

2015

Language:

english

File:

PDF, 725 KB

english, 2015

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