Ana Djarmati

2.1k total citations
29 papers, 1.3k citations indexed

About

Ana Djarmati is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Ana Djarmati has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Neurology, 16 papers in Cellular and Molecular Neuroscience and 12 papers in Molecular Biology. Recurrent topics in Ana Djarmati's work include Parkinson's Disease Mechanisms and Treatments (20 papers), Nuclear Receptors and Signaling (9 papers) and Neurological disorders and treatments (9 papers). Ana Djarmati is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (20 papers), Nuclear Receptors and Signaling (9 papers) and Neurological disorders and treatments (9 papers). Ana Djarmati collaborates with scholars based in Germany, Serbia and United States. Ana Djarmati's co-authors include Christine Klein, Katja Hedrich, Johann Hagenah, Peter P. Pramstaller, Henry L. Paulson, Vladimir Kostić, Thora Lohnau, Norbert Brüggemann, Hartwig R. Siebner and Robert Hering and has published in prestigious journals such as Molecular Cell, Neurology and Biological Psychiatry.

In The Last Decade

Ana Djarmati

29 papers receiving 1.3k citations

Peers

Countries citing papers authored by Ana Djarmati

Since Specialization

Citations

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

Fields of papers citing papers by Ana Djarmati

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ana Djarmati

This figure shows the co-authorship network connecting the top 25 collaborators of Ana Djarmati. A scholar is included among the top collaborators of Ana Djarmati 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 Ana Djarmati. Ana Djarmati 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	Recessively Inherited Parkinsonism 2010 ·Archives of Neurology ·Norbert Brüggemann, Johann Hagenah, Kathrin Reetz, Alexander Schmidt, Meike Kasten, Inga Buchmann, (unknown), (unknown), Alexander Münchau, Ana Djarmati, (unknown), Hartwig R. Siebner, Ferdinand Binkofski, Alfredo Ramı́rez, María Isabel Behrens, Christine Klein	68
2	The Machado–Joseph disease-associated mutant form of ataxin-3 regulates parkin ubiquitination and stability 2010 ·Human Molecular Genetics ·Thomas M. Durcan, Maria Kontogiannea, (unknown), Lara Fallon, Aislinn Williams, Ana Djarmati, Tadeu A. Fantaneanu, Henry L. Paulson, Edward A. Fon	123
3	Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15 2010 ·Movement Disorders ·Anne Weißbach, Ana Djarmati, Christine Klein, Nataša Dragašević, Christine Zühlke, Aleksandar Raković, Miodrag Gužvić, Elisabeth Butz, Holger Tönnies, Reiner Siebert, Igor Petrović, Marina Svetel, Vladimir Kostić, Katja Lohmann	2
4	Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers 2009 ·Parkinsonism & Related Disorders ·Norbert Brüggemann, Manfred Mitterer, (unknown), Ana Djarmati, Johann Hagenah, Karin Wiegers, Susen Winkler, Heike Pawlack, Thora Lohnau, Peter P. Pramstaller, Christine Klein, Katja Lohmann	35
5	Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study 2009 ·The Lancet Neurology ·Ana Djarmati, Susanne A. Schneider, Katja Lohmann, Susen Winkler, Heike Pawlack, Johann Hagenah, Norbert Brüggemann, Simone Zittel, Tania Fuchs, Aleksandar Raković, Alexander Schmidt, Hans‐Christian Jabusch, Robert A. Wilcox, Vladimir Kostić, Hartwig R. Siebner, Eckart Altenmüller, Alexander Münchau, Laurie J. Ozelius, Christine Klein	94
6	ATP13A2 variants in early‐onset Parkinson's disease patients and controls 2009 ·Movement Disorders ·Ana Djarmati, Johann Hagenah, Kathrin Reetz, Susen Winkler, María Isabel Behrens, Heike Pawlack, Katja Lohmann, Alfredo Ramı́rez, Vera Tadić, Norbert Brüggemann, Daniela Berg, Hartwig R. Siebner, Anthony E. Lang, Peter P. Pramstaller, Ferdinand Binkofski, Vladimir Kostić, Jens Volkmann, Thomas Gasser, Christine Klein	55
7	Genetic association study of the P‐type ATPase ATP13A2 in late‐onset Parkinson's disease 2008 ·Movement Disorders ·Aleksandar Raković, Barbara Stiller, Ana Djarmati, Antònia Flaquer, Jan Freudenberg, (unknown), Michael Linnebank, Vladimir Kostić, Katja Lohmann, Sebastian Paus, Peter Nürnberg, Christian Kubisch, Christine Klein, Ullrich Wüllner, Alfredo Ramı́rez	10
8	LRRK2 and Parkin mutations in a family with parkinsonism—Lack of genotype–phenotype correlation 2008 ·Neurobiology of Aging ·Connie Marras, Christine Klein, Anthony E. Lang, Yosuke Wakutani, Danielle Moreno, Christine Sato, (unknown), Renato P. Munhoz, Katja Lohmann, Ana Djarmati, Andrew S. Bi, Ekaterina Rogaeva	7
9	Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations 2008 ·Journal of Neurology Neurosurgery & Psychiatry ·J. Hagenah, Björn Becker, Norbert Brüggemann, Ana Djarmati, Katja Lohmann, Andreas Sprenger, Christine Klein, G. Seidel	45
10	Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation‐dependent probe amplification 2007 ·Movement Disorders ·Ana Djarmati, Miodrag Gužvić, Anne Grünewald, Anthony E. Lang, Peter P. Pramstaller, David K. Simon, Angela M. Kaindl, P. Vieregge, Anders O.H. Nygren, Christian Beetz, Katja Hedrich, Christine Klein	9
11	MECP2 mutations in Serbian Rett syndrome patients 2007 ·Acta Neurologica Scandinavica ·Ana Djarmati, Valerija Dobričić, (unknown), Phil Marsh, (unknown), C Klein, Milena Djurić, Stanka Romac	2
12	Phenotypic spectrum of PINK1‐associated parkinsonism in 15 mutation carriers from 1 family 2006 ·Movement Disorders ·Anja Hiller, Johann Hagenah, Ana Djarmati, Katja Hedrich, Kathrin Reetz, Christiane Schneider‐Gold, (unknown), Alexander Münchau, Christine Klein	18
13	Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations 2006 ·Journal of Neurology Neurosurgery & Psychiatry ·Susanne Steinlechner, (unknown), (unknown), Ana Djarmati, Jannis Hagenah, Anja Hiller, Katja Hedrich, Inke R. König, Christine Klein, Rebekka Lencer	50
14	Intrafamilial phenotypic and genetic heterogeneity of dystonia 2006 ·Journal of the Neurological Sciences ·Vladimir Kostić, Marina Svetel, Kemal Kabakci, Aleksandar J. Ristić, Igor Petrović, Birgitt Schüle, Norman Kock, Ana Djarmati, Stanka Romac, Christine Klein	9
15	Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients 2006 ·Movement Disorders ·Cindy Zadikoff, Ekaterina Rogaeva, Ana Djarmati, Christine Sato, Shabnam Salehi‐Rad, Peter St George‐Hyslop, Christine Klein, Anthony E. Lang	25
16	PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism 2005 ·European Journal of Human Genetics ·Christine Klein, Ana Djarmati, Katja Hedrich, (unknown), Cesa Scaglione, Roberta Marchese, Norman Kock, Birgitt Schüle, Anja Hiller, Thora Lohnau, Susen Winkler, Karin Wiegers, Robert Hering, Peter Bauer, Olaf Rieß, Giovanni Abbruzzese, Paolo Martinelli, Peter P. Pramstaller	92
17	Co‐occurrence of restless legs syndrome and Parkin mutations in two families 2005 ·Movement Disorders ·(unknown), Ana Djarmati, Kemal Kabakci, Irene Pichler, (unknown), Thora Lohnau, Norman Kock, Johann Hagenah, Katja Hedrich, E. Schwinger, Patricia L. Kramer, Peter P. Pramstaller, Christine Klein	26
18	Detection ofParkin(PARK2) andDJ1(PARK7) mutations in early-onset Parkinson disease:Parkinmutation frequency depends on ethnic origin of patients 2004 ·Human Mutation ·Ana Djarmati, Katja Hedrich, Marina Svetel, (unknown), Vladislava Juric, Slobodanka Vukosavić, Robert Hering, Olaf Rieß, Stanka Romac, Christine Klein, Vladimir Kostić	66
19	Spinocerebellar ataxia type 17 in the Yugoslav population 2003 ·Acta Neurologica Scandinavica ·Andrej Alendar, (unknown), (unknown), Ana Djarmati, (unknown), Aleksandar J. Ristić, Nataša Dragašević, (unknown), Stanka Romac	5
20	SCA2 and SCA3 mutations in young‐onset dopa‐responsive parkinsonism 2003 ·European Journal of Neurology ·Marina Svetel, Ana Djarmati, Nataša Dragašević, (unknown), Biljana Čuljković, Stanka Romac, Vladimir Kostić	4

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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