Diana Mitter

2.3k total citations
28 papers, 923 citations indexed

About

Diana Mitter is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Diana Mitter has authored 28 papers receiving a total of 923 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 13 papers in Genetics and 5 papers in Cell Biology. Recurrent topics in Diana Mitter's work include Genomic variations and chromosomal abnormalities (5 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (3 papers). Diana Mitter is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (3 papers). Diana Mitter collaborates with scholars based in Germany, Poland and Netherlands. Diana Mitter's co-authors include Gudrun Ahnert‐Hilger, Karin Buiting, Deniz Kanber, Hanno J. Bolz, Sowmya V. Yelamanchili, Elena Aller, J. Lamprecht, Peter Charbel Issa, Hendrik P. N. Scholl and Bernhard Jurklies and has published in prestigious journals such as Annals of Neurology, Journal of Neurochemistry and PLoS Genetics.

In The Last Decade

Diana Mitter

28 papers receiving 865 citations

Peers

Countries citing papers authored by Diana Mitter

Since Specialization

Citations

This map shows the geographic impact of Diana Mitter'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 Diana Mitter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Diana Mitter more than expected).

Fields of papers citing papers by Diana Mitter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Diana Mitter. 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 Diana Mitter. The network helps show where Diana Mitter may publish in the future.

Co-authorship network of co-authors of Diana Mitter

This figure shows the co-authorship network connecting the top 25 collaborators of Diana Mitter. A scholar is included among the top collaborators of Diana Mitter 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 Diana Mitter. Diana Mitter 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	Diagnose einer myotonen Dystrophie Typ1 (DM1) bei Kind mit pränatal gesicherter Trisomie 21 nach Erstdiagnose einer DM1 bei der Mutter 2022 ·Ultraschall in der Medizin - European Journal of Ultrasound ·(unknown), Diana Mitter, (unknown), Axel Sauerwald, (unknown)	1
2	Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities 2017 ·American Journal of Medical Genetics Part A ·Denise Horn, Eberhard Siebert, Ulrich Seidel, Imma Rost, Karin Mayer, Rami Abou Jamra, Diana Mitter, Uwe Kornak	20
3	Identification of a Novel Point Mutation in theLEMD3Gene in an Infant With Buschke-Ollendorff Syndrome 2016 ·JAMA Dermatology ·(unknown), Diana Mitter, Mirjana Ziemer, Jürgen Kohlhase, Harald Voth	1
4	Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C 2013 ·Aging ·(unknown), Peter Meinke, Daria Camozzi, Elisabetta Mattioli, Roland Pfaeffle, (unknown), W. Hirsch, Lars Christian Horn, Uwe Paasch, Diana Mitter, Giovanna Lattanzi, Manfred Wehnert, Wieland Kieß	12
5	MOTA Syndrome: Molecular Genetic Confirmation of the Diagnosis in a Newborn with Previously Unreported Clinical Features 2012 ·Molecular Syndromology ·Diana Mitter, Denny Schanze, Ina Sterker, D. P. R. Muller, Holger Till, Martin Zenker	9
6	Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin 2012 ·Molecular Syndromology ·Mahdi Ghani, Peter N. Robinson, Susanne Morlot, Diana Mitter, Marc Trimborn, (unknown), Raymonda Varon, Karl Sperling, Heidemarie Neitzel	15
7	A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring 2012 ·European Journal of Human Genetics ·Andreas Rump, (unknown), Andreas Tzschach, Reinhard Ullmann, Evelin Schröck, Diana Mitter	14
8	Genotype–phenotype correlations in patients with retinoblastoma and interstitial 13q deletions 2011 ·European Journal of Human Genetics ·Diana Mitter, Reinhard Ullmann, (unknown), Ludger Klein‐Hitpaß, Deniz Kanber, Katrin Õunap, Marc Kaulisch, (unknown)	76
9	Genotype–phenotype correlation in eight new patients with a deletion encompassing 2q31.1 2010 ·American Journal of Medical Genetics Part A ·Diana Mitter, Barbara Delle Chiaie, Hermann‐Josef Lüdecke, Gabriele Gillessen‐Kaesbach, Axel Bohring, Jürgen Kohlhase, Almuth Caliebe, Reiner Siebert, (unknown), María A. Ramos-Arroyo, (unknown), Björn Menten, Bart Loeys, Geert Mortier, Dagmar Wieczorek	39
10	The Human Retinoblastoma Gene Is Imprinted 2009 ·PLoS Genetics ·Deniz Kanber, Tea Berulava, Ole Ammerpohl, Diana Mitter, Julia Richter, Reiner Siebert, Bernhard Horsthemke, Dietmar Lohmann, Karin Buiting	92
11	Expanded clinical spectrum of spondylocarpotarsal synostosis syndrome and possible manifestation in a heterozygous father 2008 ·American Journal of Medical Genetics Part A ·Diana Mitter, Deborah Krakow, (unknown), Peter Meinecke	18
12	Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma 2008 ·Familial Cancer ·Diana Mitter, Diane Rushlow, (unknown), (unknown), Brenda L. Gallie, Dietmar Lohmann	8
13	Estrogen receptor β1 exerts antitumoral effects on SK-OV-3 ovarian cancer cells 2007 ·Journal of Endocrinology ·Oliver Treeck, Georg Pfeiler, Diana Mitter, Claus Lattrich, (unknown), Olaf Ortmann	89
14	Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation‐specific PCR 2006 ·American Journal of Medical Genetics Part A ·Diana Mitter, Karin Buiting, Ferdinand von Eggeling, Alma Kuechler, Thomas Liehr, Ulrike A. Mau‐Holzmann, Eva‐Christina Prott, Dagmar Wieczorek, Gabriele Gillessen‐Kaesbach	71
15	A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss 2006 ·Human Genetics ·Inga Ebermann, Hendrik P. N. Scholl, Peter Charbel Issa, Elvir Bećirović, J. Lamprecht, Bernhard Jurklies, José M. Millán, Elena Aller, Diana Mitter, Hanno J. Bolz	173
16	Östrogenrezeptor-β-Isoformen -Funktionen und klinische Bedeutung bei Brustkrebs 2005 ·Zentralblatt für Gynäkologie ·Diana Mitter, Olaf Ortmann, Oliver Treeck	2
17	The synaptophysin/synaptobrevin complex dissociates independently of neuroexocytosis 2004 ·Journal of Neurochemistry ·Clemens Reisinger, Sowmya V. Yelamanchili, (unknown), Diana Mitter, Anja Becher, Hans Bigalke, Gudrun Ahnert‐Hilger	40
18	The synaptophysin/synaptobrevin interaction critically depends on the cholesterol content 2002 ·Journal of Neurochemistry ·Diana Mitter, Clemens Reisinger, (unknown), Susanne Hollmann, Sowmya V. Yelamanchili, S. Treiber-Held, Thomas G. Ohm, Andreas Herrmann, Gudrun Ahnert‐Hilger	102
19	Meine Erfahrungen als Tutorin einer Anamnesegruppe 2001 ·Diana Mitter, Jens Jakob	1
20	Activity-dependent changes of the presynaptic synaptophysin-synaptobrevin complex in adult rat brain 2001 ·European Journal of Cell Biology ·(unknown), Anja Becher, Diana Mitter, Katrin Schulze, Uwe Heinemann, Andreas Draguhn, Gudrun Ahnert‐Hilger	52

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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