Moritz Meins

1.6k citations

27 papers · 894 indexed · h-index 17

Co-authors: F. Hanefeld Franco Laccone Peter Huppke Ralf Ulrich Trappe Wolfgang Engel Joana Cobilanschi Jane C. Sowden Eckart Apfelstedt-Sylla
Topics: RNA regulation and disease (7 papers)Genomic variations and chromosomal abnormalities (6 papers)RNA Research and Splicing (6 papers)
Cited by: Sensory Systems Genetics Molecular Biology
Journals: The American Journal of Human Genetics Human Molecular Genetics Genomics
Partner nations: Germany United States United Kingdom

In The Last Decade

Moritz Meins

27 papers receiving 862 citations

Peers

Countries citing papers authored by Moritz Meins

Since Specialization

Citations

This map shows the geographic impact of Moritz Meins's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Moritz Meins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Moritz Meins more than expected).

Fields of papers citing papers by Moritz Meins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Moritz Meins. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Moritz Meins. The network helps show where Moritz Meins may publish in the future.

Co-authorship network of co-authors of Moritz Meins

This figure shows the co-authorship network connecting the top 25 collaborators of Moritz Meins. A scholar is included among the top collaborators of Moritz Meins based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Moritz Meins. Moritz Meins is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin 2012 ·Cytogenetic and Genome Research ·Elisabeth Klein,Mariano Rocchi,(unknown),Nadezda Kosyakova,Anja Weise,Monika Ziegler,Moritz Meins,Susanne Morlot,W. Fischer,Marianne Volleth,A. Polityko,Caroline Mackie Ogilvie,Cornelia Kraus,Thomas Liehr	15
2	10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences 2009 ·Cytogenetic and Genome Research ·Thomas Liehr,Markus Stümm,R.‐D. Wegner,Samarth Bhatt,(unknown),Philippos C. Patsalis,Moritz Meins,Susanne Morlot,(unknown),Elisabeth Ewers,Sophie Hinreiner,Kristin Mrasek,Nadezda Kosyakova,(unknown),Sau Wai Cheung,Anja Weise	27
3	Mice deficient for RNA‐binding protein brunol1 show reduction of spermatogenesis but are fertile 2007 ·Molecular Reproduction and Development ·Arvind Dev,Karim Nayernia,Moritz Meins,Ibrahim M. Adham,(unknown),Wolfgang Engel	22
4	Novel Mutations in Exon 6 of the GFAP Gene Affect a Highly Conserved IF Motif in the Rod Domain 2B and are Associated with Early Onset Infantile Alexander Disease 2007 ·Neuropediatrics ·Hans Hartmann,(unknown),Ulrich Stephani,(unknown),Frank Donnerstag,Thomas Lücke,(unknown),H.‐J. Christen,(unknown),Moritz Meins	4
5	Severe Guillain–Barré syndrome associated with chromosome 17p11.2‐12 duplication 2007 ·Muscle & Nerve ·Christoph Münch,Jörg T. Epplen,Moritz Meins,R. Scott Meyer,Jörg R. Weber,Thomas Meyer	11
6	Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2) 2006 ·BMC Medical Genetics ·(unknown),Matthias Vorgerd,(unknown),(unknown),(unknown),Jörg T. Epplen,Moritz Meins	56
7	Electrophoresis of DNA in human genetic diagnostics – state‐of‐the‐art, alternatives and future prospects 2006 ·Electrophoresis ·(unknown),(unknown),Larissa Arning,Gabriele Dekomien,(unknown),Erdmute Kunstmann,Moritz Meins,Stefan Wieczorek,Jörg T. Epplen,Sabine Hoffjan	16
8	Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24‐q26.31 with minimal overlap to the dup(3q) critical region 2004 ·American Journal of Medical Genetics Part A ·Moritz Meins,(unknown),(unknown),(unknown),(unknown),(unknown),Jörg T. Epplen	15
9	A Novel <i>GFAP</i> Mutation and Disseminated White Matter Lesions: Adult Alexander Disease? 2003 ·European Neurology ·Knut Brockmann,Moritz Meins,(unknown),Ralf Ulrich Trappe,Martin Grond,F. Hanefeld	19
10	First non‐mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter → q22.1::q22.1 → pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome 2003 ·American Journal of Medical Genetics Part A ·Moritz Meins,(unknown),A. Großmann,Egbert Herting,Bernhard Fleckenstein,Christine Fauth,Michael R. Speicher,R. Schindler,Barbara Zoll,Iris Bartels,Peter Burfeind	7
11	Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10 2002 ·Human Mutation ·Barbara Zoll,(unknown),Katrin Lange,Peter Gabriel,Christiane Kiese-Himmel,(unknown),Joachim Berger,Bastian Pasche,Moritz Meins,Manfred Gross,(unknown),E. Kruse,(unknown),Karl Sperling,Franco Laccone	37
12	A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis 2002 ·Cytogenetic and Genome Research ·Ralf Ulrich Trappe,(unknown),Jürgen Kohlhase,Anja Weise,Thomas Liehr,(unknown),Moritz Meins,Barbara Zoll,Iris Bartels,Peter Burfeind	11
13	Infantile Alexander Disease: AGFAPMutation in Monozygotic Twins and Novel Mutations in Two Other Patients 2002 ·Neuropediatrics ·Moritz Meins,Knut Brockmann,Shobha Yadav,(unknown),(unknown),Ulrich Stephani,F. Hanefeld	25
14	Identification and characterization of murine <i>Brunol4</i>, a new member of the elav/bruno family 2002 ·Cytogenetic and Genome Research ·Moritz Meins,(unknown),Christian Wilhelm,(unknown),Shobha Yadav,Birgitta Gläser,Michal Grzmil,Patricia Burfeind,Franco Laccone	16
15	Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions 2001 ·Human Mutation ·Franco Laccone,Peter Huppke,F. Hanefeld,Moritz Meins	66
16	MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin 2001 ·The American Journal of Human Genetics ·Ralf Ulrich Trappe,Franco Laccone,Joana Cobilanschi,Moritz Meins,Peter Huppke,F. Hanefeld,Wolfgang Engel	187
17	Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retina. 2001 ·PubMed ·Jane C. Sowden,James K. L. Holt,Moritz Meins,Hazel K. Smith,Shomi S. Bhattacharya	33
18	Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis 2000 ·Human Mutation ·Ingrid Zwaenepoel,Elisabeth Verpy,S Blanchard,Moritz Meins,Eckart Apfelstedt-Sylla,Andreas Gal,Christine Petit	33
19	Characterization of the Human TBX20 Gene, a New Member of the T-Box Gene Family Closely Related to the Drosophila H15 Gene 2000 ·Genomics ·Moritz Meins,Deborah J. Henderson,(unknown),Jane C. Sowden	42
20	Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa 1994 ·Human Mutation ·(unknown),José M. Millán,Moritz Meins,Magdalena Beneyto,(unknown),Eckart Apfelstedt-Sylla,(unknown),Eberhart Zrenner,Félix Prieto,Andreas Gal	29

About Moritz Meins

Moritz Meins is a scholar working on Sensory Systems, Developmental Biology and Genetics, having authored 27 papers that have together received 894 indexed citations. Recurring topics across this work include RNA regulation and disease (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and RNA Research and Splicing (6 papers). The work is most often cited by research in Sensory Systems (105 citations), Genetics (394 citations) and Molecular Biology (615 citations). Moritz Meins has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include F. Hanefeld, Franco Laccone, Peter Huppke, Ralf Ulrich Trappe, Wolfgang Engel, Joana Cobilanschi, Jane C. Sowden, Eckart Apfelstedt-Sylla, Andreas Gal and Jörg T. Epplen. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics and Genomics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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