Philipp G Maass 个人学术档案

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引用	2198	1593
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A. Rasim BarutcuSenior Bioinformatician, ScitoVation在 scitovation.com 的电子邮件经过验证
Marta MeléGroup Leader at Barcelona Supercomputing Center在 bsc.es 的电子邮件经过验证
Kaia MattioliPostdoctoral Fellow, Brigham & Women's Hospital / Harvard Medical School在 dfci.harvard.edu 的电子邮件经过验证
David M. ShechnerAssistant Professor of Pharmacology, University of Washington在 uw.edu 的电子邮件经过验证
Andreas Rump在 tu-dresden.de 的电子邮件经过验证
Mary GoldringProfessor of Cell & Developmental Biology, Hospital for Special Surgery, Weill Cornell Medical College在 hss.edu 的电子邮件经过验证
Sigmar StrickerFreie Universität Berlin在 fu-berlin.de 的电子邮件经过验证
Nikolaus RajewskyProfessor, Systems Biology, Max Delbruck Center for Molecular Medicine, Berlin在 mdc-berlin.de 的电子邮件经过验证
Alessandro AiutiTIGET; Istituto Scientifico San Raffaele; Università Vita Salute San Raffaele在 hsr.it 的电子邮件经过验证
sebastian memczakAltos Labs在 altoslabs.com 的电子邮件经过验证
Petar GlažarMax Planck Institute for Molecular Genetics, Berlin, Germany在 molgen.mpg.de 的电子邮件经过验证
Arya M SharmaUniversity of Alberta在 ualberta.ca 的电子邮件经过验证
Maik GollaschProfessor of Medicine, University Medicine Greifswald & Charité/MDC Berlin在 charite.de 的电子邮件经过验证
Hakan R. Toka, MD, PhD, FASNManatee Memorial Hospital在 uhsinc.com 的电子邮件经过验证
Jordan Lewandowski PhDDirector, Flagship Labs在 fas.harvard.edu 的电子邮件经过验证
Pieter-Jan VoldersBioinformatician (Jessa Hospital), Guest professor (Ghent University)在 ugent.be 的电子邮件经过验证
Rafael A IrizarryProfessor, Biostatistics and Computational Biology, Dana-Farber and Harvard在 ds.dfci.harvard.edu 的电子邮件经过验证
Keegan KorthauerAssistant Professor, University of British Columbia在 stat.ubc.ca 的电子邮件经过验证
Chinmay J ShuklaChief of Staff, BridgeBio在 fas.harvard.edu 的电子邮件经过验证
Daniel AndergassenIndependent Junior Group Leader Technische Universität München在 tum.de 的电子邮件经过验证

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Philipp G Maass

Scientist, SickKids Research Institute - Assistant Professor, University of Toronto

在 sickkids.ca 的电子邮件经过验证 - 首页

Non-coding Genome Inter-chromosomal contacts lncRNAs Human Disease


标题按引用次数排序按年份排序按标题排序	引用次数引用次数	年份
A map of human circular RNAs in clinically relevant tissues PG Maass, P Glažar, S Memczak, G Dittmar, I Hollfinger, L Schreyer, ... Journal of molecular medicine 95, 1179-1189, 2017	324	2017
Long non-coding RNA in health and disease PG Maass, FC Luft, S Bähring Journal of molecular medicine 92, 337-346, 2014	268	2014
PDE3A mutations cause autosomal dominant hypertension with brachydactyly PG Maass, A Aydin, FC Luft, C Schächterle, A Weise, S Stricker, ... Nature genetics 47 (6), 647-653, 2015	186	2015
A misplaced lncRNA causes brachydactyly in humans PG Maass, A Rump, H Schulz, S Stricker, L Schulze, K Platzer, A Aydin, ... The Journal of clinical investigation 122 (11), 3990-4002, 2012	131	2012
A TAD boundary is preserved upon deletion of the CTCF-rich Firre locus AR Barutcu, PG Maass, JP Lewandowski, CL Weiner, JL Rinn Nature communications 9 (1), 1444, 2018	128	2018
High-throughput functional analysis of lncRNA core promoters elucidates rules governing tissue specificity K Mattioli, PJ Volders, C Gerhardinger, JC Lee, PG Maass, M Melé, ... Genome research 29 (3), 344-355, 2019	119	2019
High‐throughput identification of RNA nuclear enrichment sequences CJ Shukla, AL McCorkindale, C Gerhardinger, KD Korthauer, MN Cabili, ... The EMBO journal 37 (6), e98452, 2018	113	2018
Interchromosomal interactions: a genomic love story of kissing chromosomes PG Maass, AR Barutcu, JL Rinn Journal of Cell Biology 218 (1), 27-38, 2019	111	2019
Spatiotemporal allele organization by allele-specific CRISPR live-cell imaging (SNP-CLING) PG Maass, AR Barutcu, DM Shechner, CL Weiner, M Melé, JL Rinn Nature structural & molecular biology 25 (2), 176-184, 2018	91	2018
Inter-chromosomal contact properties in live-cell imaging and in Hi-C PG Maass, AR Barutcu, CL Weiner, JL Rinn Molecular cell 69 (6), 1039-1045. e3, 2018	84	2018
The BK channel β1 subunit gene is associated with human baroreflex and blood pressure regulation M Gollasch, J Tank, FC Luft, J Jordan, P Maass, C Krasko, AM Sharma, ... Journal of hypertension 20 (5), 927-933, 2002	84	2002
A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E PG Maass, J Wirth, A Aydin, A Rump, S Stricker, S Tinschert, M Otero, ... Human molecular genetics 19 (5), 848-860, 2010	71	2010
Systematic mapping of nuclear domain-associated transcripts reveals speckles and lamina as hubs of functionally distinct retained introns AR Barutcu, M Wu, U Braunschweig, BJA Dyakov, Z Luo, KM Turner, ... Molecular cell 82 (5), 1035-1052. e9, 2022	49	2022
Phosphodiesterase 3A and arterial hypertension M Ercu, L Markó, C Schächterle, D Tsvetkov, Y Cui, S Maghsodi, ... Circulation 142 (2), 133-149, 2020	45	2020
Gene silencing and a novel monoallelic expression pattern in distinct CD177 neutrophil subsets C Eulenberg-Gustavus, S Bähring, PG Maass, FC Luft, R Kettritz Journal of Experimental Medicine 214 (7), 2089-2101, 2017	45	2017
Cis and trans effects differentially contribute to the evolution of promoters and enhancers K Mattioli, W Oliveros, C Gerhardinger, D Andergassen, PG Maass, ... Genome biology 21, 1-22, 2020	43	2020
Clinical effects of phosphodiesterase 3A mutations in inherited hypertension with brachydactyly O Toka, J Tank, C Schaechterle, A Aydin, PG Maass, S Elitok, ... Hypertension 66 (4), 800-808, 2015	41	2015
Glioma gene therapy with soluble transforming growth factor-β receptors II and III U Naumann, P Maass, AK Gleske, S Aulwurm, M Weller, G Eisele International journal of oncology 33 (4), 759-765, 2008	38	2008
A noncoding single-nucleotide polymorphism at 8q24 drives IDH1-mutant glioma formation C Yanchus, KL Drucker, TM Kollmeyer, R Tsai, W Winick-Ng, M Liang, ... Science 378 (6615), 68-78, 2022	34	2022
Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNA S Bähring, M Kann, Y Neuenfeld, M Gong, D Chitayat, HR Toka, O Toka, ... Hypertension 51 (2), 426-431, 2008	32	2008

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