Siren Berland

1.9k total citations
28 papers, 478 citations indexed

About

Siren Berland is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Siren Berland has authored 28 papers receiving a total of 478 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 16 papers in Genetics and 4 papers in Physiology. Recurrent topics in Siren Berland's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and RNA modifications and cancer (4 papers). Siren Berland is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and RNA modifications and cancer (4 papers). Siren Berland collaborates with scholars based in Norway, United Kingdom and Sweden. Siren Berland's co-authors include Gunnar Houge, Per M. Knappskog, Emmanuel Tubacher, Stefan Johansson, Sheela Nampoothiri, Pierre‐Simon Jouk, Anne‐Louise Leutenegger, Charles Marcaillou, Audrey Labalme and Patrick Edery and has published in prestigious journals such as Science, The Journal of Clinical Endocrinology & Metabolism and PEDIATRICS.

In The Last Decade

Siren Berland

27 papers receiving 471 citations

Peers

Countries citing papers authored by Siren Berland

Since Specialization

Citations

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

Fields of papers citing papers by Siren Berland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Siren Berland

This figure shows the co-authorship network connecting the top 25 collaborators of Siren Berland. A scholar is included among the top collaborators of Siren Berland 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 Siren Berland. Siren Berland 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	Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies 2024 ·Investigative Ophthalmology & Visual Science ·(unknown), Ingvild Aukrust, Laurie L. Molday, (unknown), (unknown), Siren Berland, Eyvind Rødahl, Cecilie Bredrup, Ragnheiður Bragadóttir, Eirik Bratland, Robert S. Molday, Per M. Knappskog	0
2	Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study 2024 ·Annals of Clinical and Translational Neurology ·(unknown), (unknown), Siren Berland, Claus Klingenberg, Eylert Brodtkorb, Magnhild Rasmussen, Trine Tangeraas, Yngve Thomas Bliksrud, Shamima Rahman, Laurence A. Bindoff, Omar Hikmat	3
3	Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study 2024 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Janne Molnes, Siren Berland, Pål R. Njølstad, Anders Molven	3
4	The spectrum of pyridoxine dependent epilepsy across the age span: A nationwide retrospective observational study 2023 ·Epilepsy Research ·(unknown), (unknown), Trine Tangeraas, (unknown), Alma Sikiric, (unknown), (unknown), Siren Berland, Yngve Sejersted, Thorsten Gerstner, Bjørnar Hassel, Laurence A. Bindoff, Eylert Brodtkorb	7
5	Improving diagnostic precision in primary ovarian insufficiency using comprehensive genetic and autoantibody testing 2023 ·Human Reproduction ·(unknown), Eirik Bratland, Siren Berland, (unknown), Agnethe Lund, Sigríður Björnsdóttir, Eystein S. Husebye, Marianne Øksnes	6
6	Further characterization of Borjeson‐Forssman‐Lehmann syndrome in females due to de novo variants in PHF6 2022 ·Clinical Genetics ·(unknown), (unknown), Oliver Bartsch, Siren Berland, (unknown), (unknown), Ian Hayes, Purificación Marín Reina, Paul R. Mark, Francisco Martı́nez, Isabelle Maystadt, (unknown), Katharina Steindl, Antje Wiesener, Markus Zweier, Heinrich Sticht, Christiane Zweier	3
7	Fat Malabsorption and Ursodeoxycholic Acid Treatment in Children With Reduced Organic Solute Transporter‐α (SLC51A) Expression 2022 ·JPGN Reports ·Rune Rose Tronstad, Siren Berland, Erling Tjora, (unknown), Ingvild Aukrust, Kurt Kristensen, (unknown), Anders Molven, Hanns–Ulrich Marschall, Anuradha Rao, Paul A. Dawson	2
8	The blended phenotype of a germline RIT1 and a mosaic PIK3CA variant 2021 ·Molecular Case Studies ·Siren Berland, (unknown), Nicholas Hickson, Hélene Schlecht, Gunnar Houge, Sofia Douzgou	3
9	Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith–Wiedemann spectrum features 2021 ·Molecular Case Studies ·Siren Berland, Cecilie F. Rustad, (unknown), (unknown), G Turowski, Stefan Johansson, Gunnar Houge, Bjørn Ivar Haukanes	5
10	Further delineation of the clinical spectrum of White–Sutton syndrome: 12 new individuals and a review of the literature 2021 ·European Journal of Human Genetics ·Oliver Murch, (unknown), (unknown), Kay Metcalfe, Emma Hobson, Katrina Prescott, Kate Chandler, Neeti Ghali, Jenny Carmichael, Nicola Foulds, Julie Paulsen, Marie Falkenberg Smeland, Siren Berland, Andrew E. Fry	6
11	Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents 2020 ·European Journal of Human Genetics ·(unknown), Ksenia Lavrichenko, Siren Berland, Øyvind Helgeland, Gun Peggy Knudsen, Marc Vaudel, Jan Haavik, Per M. Knappskog, Pål R. Njølstad, Gunnar Houge, Stefan Johansson	44
12	Clinical features and molecular genetics of patients with ABCA4‐retinal dystrophies 2020 ·Acta Ophthalmologica ·(unknown), Ingvild Aukrust, (unknown), Siren Berland, Ove Bruland, (unknown), Tomasz Stokowy, (unknown), Vegard A. Forsaa, Dordi Austeng, Eyvind Rødahl, Cecilie Bredrup, Per M. Knappskog, Ragnheiður Bragadóttir	12
13	Birt-Hogg-Dubé-syndrom 2020 ·Tidsskrift for Den norske legeforening ·(unknown), Siren Berland, (unknown), Henrik Aamodt, Jan Cezary Sitek, Kjersti Jørgensen, Truls E. Bjerklund Johansen	2
14	A de novo Ser111Thr variant in aquaporin-4 in a patient with intellectual disability, transient signs of brain ischemia, transient cardiac hypertrophy, and progressive gait disturbance 2018 ·Molecular Case Studies ·Siren Berland, Trine L. Toft‐Bertelsen, Ingvild Aukrust, Jan Byška, Marc Vaudel, Laurence A. Bindoff, Nanna MacAulay, Gunnar Houge	3
15	Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy 2015 ·Ophthalmic Genetics ·(unknown), Siren Berland, Cecilie Bredrup, Dordi Austeng, Sten Andréasson, (unknown)	7
16	Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome 2014 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Christiane Zweier, Olaf Rittinger, Ingrid Bader, Siren Berland, Trevor Cole, Franziska Degenhardt, Nataliya Di Donato, Luitgard Graul‐Neumann, Juliane Hoyer, Sally Ann Lynch, (unknown), Dagmar Wieczorek	20
17	Evidence for anticipation in Beckwith–Wiedemann syndrome 2013 ·European Journal of Human Genetics ·Siren Berland, (unknown), Ove Bruland, Jasmin Beygo, Karin Buiting, Deborah Mackay, I. Karen Temple, Gunnar Houge	22
18	Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA 2011 ·Science ·Patrick Edery, Charles Marcaillou, Mourad Sahbatou, Audrey Labalme, Joëlle Chastang, Renaud Touraine, Emmanuel Tubacher, (unknown), Michael B. Bober, Sheela Nampoothiri, Pierre‐Simon Jouk, Elisabeth Steichen, Siren Berland, Annick Toutain, Carol A. Wise, Damien Sanlaville, Francis Rousseau, Françoise Clerget‐Darpoux, Anne‐Louise Leutenegger	159
19	<i>PHF6</i> Deletions May Cause Borjeson-Forssman-Lehmann Syndrome in Females 2010 ·Molecular Syndromology ·Siren Berland, (unknown), (unknown), Gunnar Houge, Randi Hovland	28
20	Late-onset gain of skills and peculiar jugular pit in an 11-year-old girl with 5q14.3 microdeletion including MEF2C 2010 ·Clinical Dysmorphology ·Siren Berland, Gunnar Houge	16

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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