Browse by Research Team

2023

BLN protein induces cardiac hypertrophy and failure.
Sperling, S.R.
Nature Cardiovascular Research 2 (11): 964-965. November 2023

2018

Diverging roads to the heart.
Kelly, R.G. and Sperling, S.R.
Science 359 (6380): 1098-1099. 9 March 2018

CRISPR correction of the PRKAG2 gene mutation in the patient's iPSC-derived cardiomyocytes eliminates the electrophysiological and structural abnormalities.
Ben Jehuda, R. and Eisen, B. and Shemer, Y. and Mekies, L.N. and Szantai, A. and Reiter, I. and Cui, H. and Guan, K. and Haron-Khun, S. and Freimark, D. and Sperling, S.R. and Gherghiceanu, M. and Arad, M. and Binah, O.
Heart Rhythm 15 (2): 267-276. February 2018

2017

Severe DCM phenotype of patient harboring RBM20 mutation S635A can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytes.
Streckfuss-Boemeke, K. and Tiburcy, M. and Fomin, A. and Luo, X. and Li, W. and Fischer, C. and Oezcelik, C. and Perrot, A. and Sossalla, S. and Haas, J. and Vidal, R.O. and Rebs, S. and Khadjeh, S. and Meder, B. and Bonn, S. and Linke, W.A. and Zimmermann, W.H. and Hasenfuss, G. and Guan, K.
Journal of Molecular and Cellular Cardiology 113 : 9-21. December 2017

Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.
Montag, J. and Syring, M. and Rose, J. and Weber, A.L. and Ernstberger, P. and Mayer, A.K. and Becker, E. and Keyser, B. and Dos Remedios, C. and Perrot, A. and van der Velden, J. and Francino, A. and Navarro-Lopez, F. and Ho, C.Y. and Brenner, B. and Kraft, T.
Journal of Muscle Research and Cell Motility 38 (3-4): 291-302. August 2017

Muscle-relevant genes marked by stable H3K4me2/3 profiles and enriched MyoD binding during myogenic differentiation.
Cui, H. and Bansal, V. and Grunert, M. and Malecova, B. and Dall Agnese, A. and Latella, L. and Gatto, S. and Ryan, T. and Schulz, K. and Chen, W. and Dorn, C. and Puri, P.L. and Sperling, S.R.
PLoS ONE 12 (6): e0179464. 13 June 2017

2016

Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.
Grunert, M. and Dorn, C. and Cui, H. and Dunkel, I. and Schulz, K. and Schoenhals, S. and Sun, W. and Berger, F. and Chen, W. and Sperling, S.R.
Cardiovascular Research 112 (1): 464-477. 1 October 2016

Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers.
Claes, G.R.F. and van Tienen, F.H.J. and Lindsey, P. and Krapels, I.P.C. and Helderman-van den Enden, A.T.J.M. and Hoos, M.B. and Barrois, Y.E.G. and Janssen, J.W.H. and Paulussen, A.D.C. and Sels, J.W.E.M. and Kuijpers, S.H.H. and van Tintelen, J.P. and van den Berg, M.P. and Heesen, W.F. and Garcia-Pavia, P. and Perrot, A. and Christiaans, I. and Salemink, S. and Marcelis, C.L.M. and Smeets, H.J.M. and Brunner, H.G. and Volders, P.G.A. and van den Wijngaard, A.
European Heart Journal 37 (23): 1815-1822. 14 June 2016

Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA.
Cui, H. and Schlesinger, J. and Schoenhals, S. and Toenjes, M. and Dunkel, I. and Meierhofer, D. and Cano, E. and Schulz, K. and Berger, M.F. and Haack, T. and Abdelilah-Seyfried, S. and Bulyk, M.L. and Sauer, S. and Sperling, S.R.
Nucleic Acids Research 44 (6): 2538-2553. 7 April 2016

Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.
Perrot, A. and Tomasov, P. and Villard, E. and Faludi, R. and Melacini, P. and Lossie, J. and Lohmann, N. and Richard, P. and De Bortoli, M. and Angelini, A. and Varga-Szemes, A. and Sperling, S.R. and Simor, T. and Veselka, J. and Oezcelik, C. and Charron, P.
Archives of Medical Science 12 (2): 263-278. April 2016

Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology-a position statement of the development, anatomy, and pathology ESC Working Group.
Perez-Pomares, J.M. and de la Pompa, J.L. and Franco, D. and Henderson, D. and Ho, S.Y. and Houyel, L. and Kelly, R.G. and Sedmera, D. and Sheppard, M. and Sperling, S. and Thiene, G. and van den Hoff, M. and Basso, C.
Cardiovascular Research 109 (2): 204-216. 1 February 2016

Cardiac transcription factors and regulatory networks.
Grunert, M. and Dorn, C. and Rickert-Sperling, S.
In: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. Springer, Vienna, 139-152. ISBN 978-3-7091-1882-5 2016

Congenital heart diseases: the broken heart : clinical features, human genetics and molecular pathways.
Rickert-Sperling, S. and Kelly, R.G. and Driscoll, D.J.
Springer, Vienna. ISBN 978-3-7091-1882-5 2016

Human genetics of defects of situs.
Perrot, A. and Rickert-Sperling, S.
In: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. Springer, Vienna, 463-472. ISBN 978-3-7091-1882-5 2016

Human genetics of tetralogy of fallot and double outlet right ventricle.
Dorn, C. and Perrot, A. and Rickert-Sperling, S.
In: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. Springer, Vienna, 403-416. ISBN 978-3-7091-1882-5 2016

Human genetics of ventricular septal defect.
Bellmann, K. and Perrot, A. and Rickert-Sperling, S.
In: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. Springer, Vienna, 307-328. ISBN 978-3-7091-1882-5 2016

Preface.
Rickert-Sperling, S. and Kelly, R.G. and Driscoll, D.J.
Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways : ix-x. 2016

Technologies to study genetics and molecular pathways.
Dorn, C. and Grunert, M. and Dopazo, A. and Sanchez-Cabo, F. and Gatto, A. and Vazquez, J. and Rickert-Sperling, S. and Lara-Pezzi, E.
In: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. Springer, Vienna, 251-269. ISBN 978-3-7091-1882-5 2016

2015

ZBTB17 (MIZ1) is important for the cardiac stress response and a novel candidate gene for cardiomyopathy and heart failure.
Buyandelger, B. and Mansfield, C. and Kostin, S. and Choi, O. and Roberts, A.M. and Ware, J.S. and Mazzarotto, F. and Pesce, F. and Buchan, R. and Isaacson, R.L. and Vouffo, J. and Gunkel, S. and Knoell, G. and McSweeney, S.J. and Wei, H. and Perrot, A. and Pfeiffer, C. and Toliat, M.R. and Ilieva, K. and Krysztofinska, E. and López-Olañeta, M.M. and Gómez-Salinero, J.M. and Schmidt, A. and Ng, K.E. and Teucher, N. and Chen, J. and Teichmann, M. and Eilers, M. and Haverkamp, W. and Regitz-Zagrosek, V. and Hasenfuss, G. and Braun, T. and Pennell, D.J. and Gould, I. and Barton, P.J.R. and Lara-Pezzi, E. and Schäfer, S. and Hübner, N. and Felkin, L.E. and O'Regan, D.P. and Petretto, E. and Brand, T. and Milting, H. and Nürnberg, P. and Schneider, M.D. and Prasad, S. and Knöll, R.
Circulation Cardiovascular Genetics 8 (5): 643-652. October 2015

The proepicardium keeps a potential for glomerular marker expression which supports its evolutionary origin from the pronephros.
Cano, E. and Carmona, R. and Velecela, V. and Martinez-Estrada, O. and Munoz-Chapuli, R.
Evolution & Development 17 (4): 224-230. July 2015

CCN1 mutation is associated with atrial septal defect.
Perrot, A. and Schmitt, K.R. and Roth, E.M. and Stiller, B. and Posch, M.G. and Browne, E.N.L. and Timmann, C. and Horstmann, R.D. and Berger, F. and Ozcelik, C.
Pediatric Cardiology 36 (2): 295-299. February 2015

A promoter polymorphism -945C>G in the connective tissue growth factor in heart failure patients with mechanical circulatory support: a new marker for bridge to recovery?
Posch, M.G. and Schmidt, G. and Steinhoff, L. and Perrot, A. and Drews, T. and Dandel, M. and Krabatsch, T. and Hetzer, R. and Potapov, E.V.
European Journal of Cardio-Thoracic Surgery 47 (1): e29-e33. 2015

2014

Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.
Grunert, M. and Dorn, C. and Schueler, M. and Dunkel, I. and Schlesinger, J. and Mebus, S. and Alexi-Meskishvili, V. and Perrot, A. and Wassilew, K. and Timmermann, B. and Hetzer, R. and Berger, F. and Sperling, S.R.
Human Molecular Genetics 23 (12): 3115-3128. 15 June 2014

Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot.
Bansal, V. and Dorn, C. and Grunert, M. and Klaassen, S. and Hetzer, R. and Berger, F. and Sperling, S.R.
PLoS ONE 9 (1): e85375. 6 January 2014

Application of high-throughput sequencing for studying genomic variations in congenital heart disease.
Dorn, C. and Grunert, M. and Sperling, S.R.
Briefings in Functional Genomics 13 (1): 51-65. January 2014

2013

Variations in the human soluble epoxide hydrolase gene and recurrence of atrial fibrillation after catheter ablation.
Wutzler, A. and Kestler, C. and Perrot, A. and Loehr, L. and Huemer, M. and Parwani, A.S. and Attanasio, P. and Özcelik, C. and Schunck, W.H. and Gollasch, M. and Haverkamp, W. and Boldt, L.H.
International Journal of Cardiology 168 (4): 3647-3651. 9 October 2013

Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy.
Roncarati, R. and Viviani Anselmi, C. and Krawitz, P. and Lattanzi, G. and von Kodolitsch, Y. and Perrot, A. and di Pasquale, E. and Papa, L. and Portararo, P. and Columbaro, M. and Forni, A. and Faggian, G. and Condorelli, G. and Robinson, P.N.
European Journal of Human Genetics 21 (10): 1105-1111. October 2013

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
van Rijsingen, I.A.W. and Nannenberg, E.A. and Arbustini, E. and Elliott, P.M. and Mogensen, J. and Hermans-van Ast, J.F. and van der Kooi, A.J. and van Tintelen, J.P. and van den Berg, M.P. and Grasso, M. and Serio, A. and Jenkins, S. and Rowland, C. and Richard, P. and Wilde, A.A.M. and Perrot, A. and Pankuweit, S. and Zwinderman, A.H. and Charron, P. and Christiaans, I. and Pinto, Y.M.
European Journal of Heart Failure 15 (4): 376-384. April 2013

Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7.
van Engelen, K. and Postma, A.V. and van de Meerakker, J.B.A. and Roos-Hesselink, J.W. and Helderman-van den Enden, A.T.J.M. and Vliegen, H.W. and Rahman, T. and Baars, M.J.H. and Sels, J.W. and Bauer, U. and Pickardt, T. and Sperling, S.R. and Moorman, A.F.M. and Keavney, B. and Goodship, J. and Klaassen, S. and Mulder, B.J.
Netherlands Heart Journal 21 (3): 113-117. March 2013

Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.
Meyer, T. and Ruppert, V. and Ackermann, S. and Richter, A. and Perrot, A. and Sperling, S.R. and Posch, M.G. and Maisch, B. and Pankuweit, S.
European Journal of Human Genetics 21 (3): 294-300. March 2013

2012

Dynamics of Srf, p300 and histone modifications during cardiac maturation in mouse.
Schueler, M. and Zhang, Q. and Schlesinger, J. and Toenjes, M. and Sperling, S.R.
Molecular BioSystems 8 (2): 495-503. February 2012

Risk factors for malignant ventricular arrhythmias in lamin A/C mutation carriers a European cohort study.
van Rijsingen, I.A.W. and Arbustini, E. and Elliott, P.M. and Mogensen, J. and Hermans-van Ast, J.F. and van der Kooi, A.J. and van Tintelen, J.P. and van den Berg, M.P. and Pilotto, A. and Pasotti, M. and Jenkins, S. and Rowland, C. and Aslam, U. and Wilde, A.A.M. and Perrot, A. and Pankuweit, S. and Zwinderman, A.H. and Charron, P. and Pinto, Y.M.
Journal of the American College of Cardiology 59 (5): 493-500. 31 January 2012

2011

Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.
Posch, M.G. and Waldmuller, S. and Mueller, M. and Scheffold, T. and Fournier, D. and Andrade-Navarro, M.A. and De Geeter, B. and Guillaumont, S. and Dauphin, C. and Yousseff, D. and Schmitt, K.R. and Perrot, A. and Berger, F. and Hetzer, R. and Bouvagnet, P. and Ozcelik, C.
PLoS ONE 6 (12): e28872. 14 December 2011

Unequal allelic expression of wild-type and mutated beta-myosin in familial hypertrophic cardiomyopathy.
Tripathi, S. and Schultz, I. and Becker, E. and Montag, J. and Borchert, B. and Francino, A. and Navarro-Lopez, F. and Perrot, A. and Oezcelik, C. and Osterziel, K.J. and McKenna, W.J. and Brenner, B. and Kraft, T.
Basic Research in Cardiology 106 (6): 1041-1055. November 2011

Systems biology approaches to heart development and congenital heart disease.
Sperling, S.R.
Cardiovascular Research 91 (2): 269-278. 15 July 2011

Mutations in the sarcomere protein gene MYH7 in Ebstein's anomaly.
Postma, A.V. and van Engelen, K. and van de Meerakker, J. and Rahman, T. and Probst, S. and Baars, M.J. and Bauer, U. and Pickardt, T. and Sperling, S.R. and Berger, F. and Moorman, A.F. and Mulder, B.J. and Thierfelder, L. and Keavney, B. and Goodship, J. and Klaassen, S.
Circulation Cardiovascular Genetics 4 (1): 43-50. February 2011

The cardiac transcription network modulated by Gata4, Mef2a, Nkx2.5, Srf, histone modifications, and microRNAs.
Schlesinger, J. and Schueler, M. and Grunert, M. and Fischer, J.J. and Zhang, Q. and Krueger, T. and Lange, M. and Toenjes, M. and Dunkel, I. and Sperling, S.R.
PLoS Genetics 7 (2): e1001313. February 2011

2010

The effect of micrococcal nuclease digestion on nucleosome positioning data.
Chung, H.R. and Dunkel, I. and Heise, F. and Linke, C. and Krobitsch, S. and Ehrenhofer-Murray, A.E. and Sperling, S.R. and Vingron, M.
PLoS ONE 5 (12): e15754. 29 December 2010

Identification of Y-box binding protein 1 as a core regulator of MEK/ERK pathway-dependent gene signatures in colorectal cancer cells.
Juerchott, K. and Kuban, R.J. and Krech, T. and Blüthgen, N. and Stein, U. and Walther, W. and Friese, C. and Kielbasa, S.M. and Ungethuem, U. and Lund, P. and Knoesel, T. and Kemmner, W. and Morkel, M. and Fritzmann, J. and Schlag, P.M. and Birchmeier, W. and Krueger, T. and Sperling, S. and Sers, C. and Royer, H.D. and Herzel, H. and Schaefer, R.
PLoS Genetics 6 (12): e1001231. 2 December 2010

Evaluation of the LightCycler 1536 Instrument for high-throughput quantitative real-time PCR.
Schlesinger, J. and Toenjes, M. and Schueler, M. and Zhang, Q. and Dunkel, I. and Sperling, S.R.
Methods 50 (4): S19-S22. April 2010

MicroRazerS: rapid alignment of small RNA reads.
Emde, A.K. and Grunert, M. and Weese, D. and Reinert, K. and Sperling, S.R.
Bioinformatics 26 (1): 123-124. 1 January 2010

2008

Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex.
Lange, M. and Kaynak, B. and Foerster, U.B. and Toenjes, M. and Fischer, J.J. and Grimm, C. and Schlesinger, J. and Just, S. and Dunkel, I. and Krueger, T. and Mebus, S. and Lehrach, H. and Lurz, R. and Gobom, J. and Rottbauer, W. and Abdelilah-Seyfried, S. and Sperling, S.
Genes & Development 22 (17): 2370-2384. 1 September 2008

Characterization of TBX20 in human hearts and its regulation by TFAP2.
Hammer, S. and Toenjes, M. and Lange, M. and Fischer, J.J. and Dunkel, I. and Mebus, S. and Grimm, C.H. and Hetzer, R. and Berger, F. and Sperling, S.
Journal of Cellular Biochemistry 104 (3): 1022-1033. 1 June 2008

BMPR IA downstream genes related to VSD.
Yang, D. and Zhang, J. and Chen, C. and Xie, M. and Sperling, S. and Fang, F. and Chen, B. and Li, X. and Zhang, H.
Pediatric Research 63 (6): 602-606. June 2008

Prediction of cardiac transcription networks based on molecular data and complex clinical phenotypes.
Toenjes, M. and Schueler, M. and Hammer, S. and Pape, U.J. and Fischer, J.J. and Berger, F. and Vingron, M. and Sperling, S.
Molecular BioSystems 4 (6): 589-598. June 2008

Combinatorial effects of four histone modifications in transcription and differentiation.
Fischer, J.J. and Toedling, J. and Krueger, T. and Schueler, M. and Huber, W. and Sperling, S.
Genomics 91 (1): 41-51. January 2008

2007

Transcriptional regulation at a glance.
Sperling, S.
BMC Bioinformatics 8 (Suppl 6): S2. 27 September 2007

Ringo--an R/Bioconductor package for analyzing ChIP-chip readouts.
Toedling, J. and Skylar, O. and Krueger, T. and Fischer, J.J. and Sperling, S. and Huber, W.
BMC Bioinformatics 8 : 221. 26 June 2007

Genomic organization of transcriptomes in mammals: Coregulation and cofunctionality.
Purmann, A. and Toedling, J. and Schueler, M. and Carninci, P. and Lehrach, H. and Hayashizaki, Y. and Huber, W. and Sperling, S.
Genomics 89 (5): 580-587. May 2007

2006

A new statistical model to select target sequences bound by transcription factors.
Pape, U.J. and Grossmann, S. and Hammer, S. and Sperling, S. and Vingron, M.
Genome Informatics 17 (1): 134-140. 2006

Array analysis applied to malformed hearts: Molecular dissection of tetralogy of Fallot.
Sperling, S.
Methods in Molecular Medicine 1 (126): 233-246. 2006

2005

Identification and functional analysis of CITED2 mutations in patients with congenital heart defects.
Sperling, S. and Grimm, C.H. and Dunkel, I. and Mebus, S. and Sperling, H.P. and Ebner, A. and Galli, R. and Lehrach, H. and Fusch, C. and Berger, F. and Hammer, S.
Human Mutation 26 (6): 575-582. December 2005

A physiogenomic approach to study the regulation of blood pressure.
Westhoff, T.H. and Scheid, S. and Toelle, M. and Kaynak, B. and Schmidt, S. and Zidek, W. and Sperling, S. and van der Giet, M.
Physiological Genomics 23 (1): 46-53. 21 September 2005

Chromosomal clustering of a human transcriptome reveals regulatory background.
Vogel, J.H. and von Heydebreck, A. and Purmann, A. and Sperling, S.
BMC Bioinformatics 6 : 230. 19 September 2005

The transcriptional landscape of the mammalian genome.
Carninci, P. and Kasukawa, T. and Katayama, S. and Gough, J. and Frith, M.C. and Maeda, N. and Oyama, R. and Ravasi, T. and Lenhard, B. and Wells, C. and Kodzius, R. and Shimokawa, K. and Bajic, V.B. and Brenner, S.E. and Batalov, S. and Forrest, A.R.R. and Zavolan, M. and Davis, M.J. and Wilming, L.G. and Aidinis, V. and Allen, J.E. and Ambesi-Impiombato, A. and Apweiler, R. and Aturaliya, R.N. and Bailey, T.L. and Bansal, M. and Baxter, L. and Beisel, K.W. and Bersano, T. and Bono, H. and Chalk, A.M. and Chiu, K.P. and Choudhary, V. and Christoffels, A. and Clutterbuck, D.R. and Crowe, M.L. and Dalla, E. and Dalrymple, B.P. and de Bono, B. and Della Gatta, G. and di Bernardo, D. and Down, T. and Engstrom, P. and Fagiolini, M. and Faulkner, G. and Fletcher, C.F. and Fukushima, T. and Furuno, M. and Futaki, S. and Gariboldi, M. and Georgii-Hemming, P. and Gingeras, G.R. and Gojobori, T. and Green, R.E. and Gustincich, S. and Harbers, M. and Hayashi, Y. and Hensch, T.K. and Hirokawa, N. and Hill, D. and Huminiecki, L. and Iacono, I. and Ikeo, K. and Iwama, A. and Ishikawa, T. and Jakt, M. and Kanapin, A. and Katoh, M. and Kawasawa, Y. and Kelso, J. and Kitamura, H. and Kitano, H. and Kollias, G. and Krishnan, S.P.T. and Kruger, A. and Kummerfeld, S.K. and Kurochkin, I.V. and Lareau, L.F. and Lazarevic, D. and Lipovich, L. and Liu, J. and Liuni, S. and McWilliam, S. and Madan Babu, M. and Madera, M. and Marchionni, L. and Matsuda, H. and Matsuzawa, S. and Miki, H. and Mignone, F. and Miyake, S. and Morris, K. and Mottagui-Tabar, S. and Mulder, N. and Nakano, N. and Nakauchi, H. and Ng, P. and Nilsson, R. and Nishiguchi, S. and Nishikawa, S. and Nori, F. and Ohara, O. and Okazaki, Y. and Orlando, V. and Pang, K.C. and Pavan, W.J. and Pavesi, G. and Pesole, G. and Petrovsky, N. and Piazza, S. and Reed, J. and Reid, J.F. and Ring, B.Z. and Ringwald, M. and Rost, B. and Ruan, Y. and Salzberg, S.L. and Sandelin, A. and Schneider, C. and Schönbach, C. and Sekiguchi, S. and Semple, C.A.M. and Seno, S. and Sessa, L. and Sheng, Y. and Shibata, Y. and Shimada, H. and Shimada, K. and Silva, D. and Sinclair, B. and Sperling, S. and Stupka, E. and Sugiura, S. and Sultana, R. and Takenaka, Y. and Taki, K. and Tammoja, K. and Tan, S.L. and Tang, S. and Taylor, M.S. and Tegner, J. and Teichmann, S.A. and Ueda, H.R. and van Nimwegen, E. and Verardo, R. and Wei, C.L. and Yagi, K. and Yamanishi, H. and Zabarovsky, E. and Zhu, S. and Zimmer, A. and Hide, W. and Bult, C. and Grimmond, S.M. and Teasdale, R.D. and Liu, E.T. and Brusic, V. and Quackenbush, J. and Wahlestedt, C. and Mattick, J.S. and Hume, D.A. and Kai, C. and Sasaki, D. and Tomaru, Y. and Fukuda, S. and Kanamori-Katayama, M. and Suzuki, M. and Aoki, J. and Arakawa, T. and Iida, J. and Imamura, K. and Itoh, M. and Kato, T. and Kawaji, H. and Kawagashira, N. and Kawashima, T. and Kojima, M. and Kondo, S. and Konno, H. and Nakano, K. and Ninomiya, N. and Nishio, T. and Okada, M. and Plessy, C. and Shibata, K. and Shiraki, T. and Suzuki, S. and Tagami, M. and Waki, K. and Watahiki, A. and Okamura-Oho, Y. and Suzuki, H. and Kawai, J. and Hayashizaki, Y.
Science 309 (5740): 1559-1563. 2 September 2005

From single cells to whole organisms.
Sperling, S.
Genome Biology 6 (13): 365. 2005

2004

d-matrix - database exploration, visualization and analysis.
Seelow, D. and Galli, R. and Mebus, S. and Sperling, H.P. and Lehrach, H. and Sperling, S.
BMC Bioinformatics 5 : 168. 28 October 2004

Multiplexed real-time PCR using universal reporters.
Rickert, A.M. and Lehrach, H. and Sperling, S.
Clinical Chemistry 50 (9): 1680-1683. September 2004

Refinement of single-nucleotide polymorphism genotyping methods on human genomic DNA: amplifluor allele-specific polymerase chain reaction versus ligation detection reaction-TaqMan.
Rickert, A.M. and Borodina, T.A. and Kuhn, E.J. and Lehrach, H. and Sperling, S.
Analytical Biochemistry 330 (2): 288-297. 15 July 2004

2003

Genome-wide array analysis of normal and malformed human hearts.
Kaynak, B. and von Heydebreck, A. and Mebus, S. and Seelow, D. and Hennig, S. and Vogel, J. and Sperling, H.P. and Pregla, R. and Alexi-Meskishvili, V. and Hetzer, R. and Lange, P.E. and Vingron, M. and Lehrach, H. and Sperling, S.
Circulation 107 (19): 2467-2474. 20 May 2003

2001

Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene.
Handschug, K. and Sperling, S. and Yoon, S.J. and Hennig, S. and Clark, A.J. and Huebner, A.
Human Molecular Genetics 10 (3): 283-290. 1 February 2001