Anna Birve

2.2k citations

20 papers · 729 indexed · h-index 14

Neurology top 5%
- Amyotrophic Lateral Sclerosis Research 13
- Parkinson's Disease Mechanisms and Treatments 5
- Neurological diseases and metabolism 2
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 10
Neurology top 10%
- Amyotrophic Lateral Sclerosis Research 13
- Parkinson's Disease Mechanisms and Treatments 5
- Neurological diseases and metabolism 2
Aging
Molecular Biology
- Glycosylation and Glycoproteins Research 3
- Epigenetics and DNA Methylation 3
- Cancer-related gene regulation 3
- Genomics and Chromatin Dynamics 3

Co-authors: Åsa Rasmuson-Lestander Peter M. Andersen Jan Larsson Jürg Müller Dirk Beuchle James A. Kennison Aditya K. Sengupta Feng Tie
Cited by: Neurology Genetics Aging
Journals: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (4 papers)Human Molecular Genetics (3 papers)PLoS ONE (2 papers)
Partner nations: Sweden United States Germany

In The Last Decade

Anna Birve

19 papers receiving 717 citations

Peers

Countries citing papers authored by Anna Birve

Since Specialization

Citations

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

Fields of papers citing papers by Anna Birve

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Anna Birve, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna Birve Line = papers co-authored together Anna Birve links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Comprehensive analysis to explain reduced or increased SOD1 enzymatic activity in ALS patients and their relatives Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·岩西浩,Anna Birve,Mariusz Berdyński,Sathish Kumar Thellakanthiah Ekambaram,Reza Rofougaran,Torbjörn Nilsson,Jonathan D. Glass,Stefan L. Marklund,Peter M. Andersen	2017	23
2	Effects of Cellular Pathway Disturbances on Misfolded Superoxide Dismutase-1 in Fibroblasts Derived from ALS Patients PLoS ONE ·岩西浩,P. Raibaud,Dale J. Lange,Markus Weber,Anna Birve,Matthis Synofzik,Jonathan D. Gilthorpe,Peter M. Andersen,Stefan L. Marklund	2016	21
3	A 50 bp deletion in the SOD1 promoter lowers enzyme expression but is not associated with ALS in Sweden Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Caroline Ingre,Anna Wuolikainen,Stefan L. Marklund,Anna Birve,Rayomand Press,Peter M. Andersen	2016	7
4	Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD Human Molecular Genetics ·Angelica Nordin,Chizuru Akimoto,Anna Wuolikainen,Joe Wexler,Pär Jonsson,Anna Birve,Stefan L. Marklund,Karin S. Graffmo,Karin Forsberg,Thomas Brännström,Peter M. Andersen	2015	76
5	The Drosophila Midkine/Pleiotrophin Homologues Miple1 and Miple2 Affect Adult Lifespan but Are Dispensable for Alk Signaling during Embryonic Gut Formation PLoS ONE ·Fredrik Hugosson,Camilla Sjögren,Anna Birve,Taye Demissie Beshi,Therése Eriksson,Ruth H. Palmer	2014	12
6	No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Caroline Ingre,Susana Pinto,Anna Birve,Rayomand Press,Olof Danielsson,Mamede de Carvalho,Grétar Guðmundsson,Peter M. Andersen	2013	10
7	No GGGGCC-hexanucleotide repeat expansion inC9ORF72in parkinsonism patients in Sweden Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Chizuru Akimoto,Lars Forsgren,Jan Linder,Anna Birve,A. Sochan,Tilahun Dessie,بهنوش کریمی مفرح,Joe Wexler,Peter M. Andersen	2012	20
8	Mutant superoxide dismutase-1 indistinguishable from wild-type causes ALS Human Molecular Genetics ·Matthis Synofzik,Dario Ronchi,岩西浩,A. Nazlı Başak,Christian Wilhelm,Claudio Gobbi,Anna Birve,Saskia Biskup,Chiara Zecca,Rubén Fernández‐Santiago,Long Sirui,Lüdger Schöls,Stefan L. Marklund,Peter M. Andersen	2012	45
9	A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany Neurobiology of Aging ·Jochen H. Weishaupt,Stefan Waibel,Anna Birve,Alexander E. Volk,Benjamin Mayer,Thomas Meyer,Albert C. Ludolph,Peter M. Andersen	2012	42
10	A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts Neurobiology of Aging ·Caroline Ingre,John E. Landers,Ezequias Márcio Silva de Santana Júnior,Alexander E. Volk,Chizuru Akimoto,Anna Birve,Annemarie Hübers,Pamela Keagle,Katarzyna Piotrowska,Rayomand Press,Peter M. Andersen,Albert C. Ludolph,Jochen H. Weishaupt	2012	67
11	A novel ALS SOD1 C6S mutation with implications for aggregation related toxicity and genetic counseling Amyotrophic Lateral Sclerosis ·Алленова Елена Николаевна,Meraida Polak,Crystal Kelly,Anna Birve,Peter M. Andersen,Stefan L. Marklund,Jonathan D. Glass	2010	18
12	A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysis Human Molecular Genetics ·Anna Birve,Christoph Neuwirth,Markus Weber,Stefan L. Marklund,بهنوش کریمی مفرح,P. Andreas Jonsson,Peter M. Andersen	2010	21
13	Analysis ofFGGYas a risk factor for sporadic amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis ·Michael A. van Es,Paul W.J. van Vught,Jan H. Veldink,Peter M. Andersen,Anna Birve,Robin Lemmens,Simon Cronin,Anneke J. van der Kooi,Marianne de Visser,Helenius J. Schelhaas,Orla Hardiman,Jiannis Ragoussis,Diether Lambrechts,Wim Robberecht,John H. J. Wokke,Roel A. Ophoff,Leonard H. van den Berg	2009	14
14	Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis ·Timotej Draksler,L H Blumgart,Jan H. Veldink,Peter Andersen,Anna Birve,Robin Lemmens,Simon Cronin,Anneke J. van der Kooi,Marianne de Visser,Helenius J. Schelhaas,Orla Hardiman,Jiannis Ragoussis,Diether Lambrechts,Wim Robberecht,John H. J. Wokke,Roel A. Ophoff,Leonard van den Berg	2009	2
15	In vivo analysis of Suppressor of zeste 12´s different isoforms Carolina Gabriela González Olivares,Khalil Shujaee,Голованова Наталья Геннадьевна,Anna Birve,刘成霞	2009	0
16	In vivo analysis of Drosophila SU(Z)12 function Molecular Genetics and Genomics ·Sa Chen,Anna Birve,Åsa Rasmuson-Lestander	2007	9
17	Sequence analyses of fimbriae subunit FimA proteins on Actinomyces naeslundii genospecies 1 and 2 and Actinomyces odontolyticus with variant carbohydrate binding specificities BMC Microbiology ·Mirva Drobni,K. Hallberg,Hongjie Zhang,Anna Birve,Karina Persson,Ingegerd Johansson,Nicklas Strömberg	2006	23
18	Miple1 and miple2 encode a family of MK/PTN homologues in Drosophila melanogaster Development Genes and Evolution ·Camilla Englund,Anna Birve,K. Shivprakash,Caroline Grabbe,Ruth H. Palmer	2005	29
19	A 1-Megadalton ESC/E(Z) Complex from Drosophila That Contains Polycomblike and RPD3 Molecular and Cellular Biology ·Feng Tie,M. Haïssinsky.,Anna Birve,Åsa Rasmuson-Lestander,Peter J. Harte	2003	113
20	Su(z)12, a novelDrosophilaPolycomb group gene that is conserved in vertebrates and plants Development ·Anna Birve,Aditya K. Sengupta,Dirk Beuchle,Jan Larsson,James A. Kennison,Åsa Rasmuson-Lestander,Jürg Müller	2001	177

About Anna Birve

Anna Birve is a scholar working on Genetics, Neurology, Neurology, Biochemistry and Molecular Biology, having authored 20 papers that have together received 729 indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (13 papers), Neurogenetic and Muscular Disorders Research (10 papers), Parkinson's Disease Mechanisms and Treatments (5 papers), Glycosylation and Glycoproteins Research (3 papers), Epigenetics and DNA Methylation (3 papers), Cancer-related gene regulation (3 papers), Genomics and Chromatin Dynamics (3 papers) and Neurological diseases and metabolism (2 papers). The work is most often cited by research in Neurology (311 citations), Genetics (186 citations), Neurology (84 citations), Aging (11 citations) and Molecular Biology (411 citations). Anna Birve has collaborated with scholars based in Sweden, United States and Germany. Frequent co-authors include Åsa Rasmuson-Lestander, Peter M. Andersen, Jan Larsson, Jürg Müller, Dirk Beuchle, James A. Kennison, Aditya K. Sengupta, Feng Tie, Peter J. Harte and Stefan L. Marklund. Their work appears in journals such as Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Human Molecular Genetics, PLoS ONE, Neurobiology of Aging and 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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