Siren Berland

1.9k citations

28 papers · 478 indexed · h-index 11

Genetics top 10%
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 5
- Congenital Ear and Nasal Anomalies 3
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 3
Molecular Biology
- RNA modifications and cancer 4
- Retinal Development and Disorders 4
- Epigenetics and DNA Methylation 3
Ophthalmology top 10%
Genetics
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 5
- Congenital Ear and Nasal Anomalies 3
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 3
Pediatrics, Perinatology and Child Health

Co-authors: Gunnar Houge Per M. Knappskog Emmanuel Tubacher Stefan Johansson Sheela Nampoothiri Pierre‐Simon Jouk Anne‐Louise Leutenegger Charles Marcaillou
Cited by: Genetics Molecular Biology Ophthalmology
Partner nations: Norway United Kingdom Sweden

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

The 25 scholars most cited alongside Siren Berland, 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 Siren Berland Line = papers co-authored together Siren Berland links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies Sigrid Aslaksen,Ingvild Aukrust,Laurie L. Molday,Josephine Prener Holtan,Ragnhild Wivestad Jansson,Siren Berland,Eyvind Rødahl,Cecilie Bredrup,Ragnheiður Bragadóttir,Eirik Bratland,Robert S. Molday,Per M. Knappskog	2024	0
2	Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study Erle Kristensen,Linda Mathisen,Siren Berland,Claus Klingenberg,Eylert Brodtkorb,Magnhild Rasmussen,Trine Tangeraas,Yngve Thomas Bliksrud,Shamima Rahman,Laurence A. Bindoff,Omar Hikmat	2024	3
3	Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study Christoffer Drabløs Velde,Janne Molnes,Siren Berland,Pål R. Njølstad,Anders Molven	2024	3
4	The spectrum of pyridoxine dependent epilepsy across the age span: A nationwide retrospective observational study Ahmed Jamali,Erle Kristensen,Trine Tangeraas,Vibeke Arntsen,Alma Sikiric,Guste Kupliauskiene,Sverre Myren‐Svelstad,Siren Berland,Yngve Sejersted,Thorsten Gerstner,Bjørnar Hassel,Laurence A. Bindoff,Eylert Brodtkorb	2023	7
5	Improving diagnostic precision in primary ovarian insufficiency using comprehensive genetic and autoantibody testing Elinor Vogt,Eirik Bratland,Siren Berland,Ragnhild Drage Berentsen,Agnethe Lund,Sigríður Björnsdóttir,Eystein S. Husebye,Marianne Øksnes	2023	6
6	Further characterization of Borjeson‐Forssman‐Lehmann syndrome in females due to de novo variants in PHF6 Céline B. Gerber,Anna Fliedner,Oliver Bartsch,Siren Berland,Malin Dewenter,Marte G. Haug,Ian Hayes,Purificación Marín Reina,Paul R. Mark,Francisco Martı́nez,Isabelle Maystadt,Deniz Karadurmus,Katharina Steindl,Antje Wiesener,Markus Zweier,Heinrich Sticht,Christiane Zweier	2022	3
7	Fat Malabsorption and Ursodeoxycholic Acid Treatment in Children With Reduced Organic Solute Transporter‐α (SLC51A) Expression Rune Rose Tronstad,Siren Berland,Erling Tjora,Khadija El Jellas,Ingvild Aukrust,Kurt Kristensen,Dag Tveitnes,Anders Molven,Hanns–Ulrich Marschall,Anuradha Rao,Paul A. Dawson	2022	2
8	The blended phenotype of a germline RIT1 and a mosaic PIK3CA variant Siren Berland,Jørgen Jareld,Nicholas Hickson,Hélene Schlecht,Gunnar Houge,Sofia Douzgou	2021	3
9	Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith–Wiedemann spectrum features Siren Berland,Cecilie F. Rustad,Mariann H. L. Bentsen,Embjørg J. Wollen,G Turowski,Stefan Johansson,Gunnar Houge,Bjørn Ivar Haukanes	2021	5
10	Further delineation of the clinical spectrum of White–Sutton syndrome: 12 new individuals and a review of the literature Oliver Murch,Vani Jain,Andreas Benneche,Kay Metcalfe,Emma Hobson,Katrina Prescott,Kate Chandler,Neeti Ghali,Jenny Carmichael,Nicola Foulds,Julie Paulsen,Marie Falkenberg Smeland,Siren Berland,Andrew E. Fry	2021	6
11	Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents Dinka Smajlagić,Ksenia Lavrichenko,Siren Berland,Øyvind Helgeland,Gun Peggy Knudsen,Marc Vaudel,Jan Haavik,Per M. Knappskog,Pål R. Njølstad,Gunnar Houge,Stefan Johansson	2020	44
12	Clinical features and molecular genetics of patients with ABCA4‐retinal dystrophies Josephine Prener Holtan,Ingvild Aukrust,Ragnhild Wivestad Jansson,Siren Berland,Ove Bruland,Birgitt Løkhaug Gjerde,Tomasz Stokowy,Ognjen Bojović,Vegard A. Forsaa,Dordi Austeng,Eyvind Rødahl,Cecilie Bredrup,Per M. Knappskog,Ragnheiður Bragadóttir	2020	12
13	Birt-Hogg-Dubé-syndrom Ingvil Berger,Siren Berland,Jezabel Rivero Rodriguez,Henrik Aamodt,Jan Cezary Sitek,Kjersti Jørgensen,Truls E. Bjerklund Johansen	2020	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 Siren Berland,Trine L. Toft‐Bertelsen,Ingvild Aukrust,Jan Byška,Marc Vaudel,Laurence A. Bindoff,Nanna MacAulay,Gunnar Houge	2018	3
15	Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy Ragnhild Wivestad Jansson,Siren Berland,Cecilie Bredrup,Dordi Austeng,Sten Andréasson,Elisabeth Wittström	2015	7
16	Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome Christiane Zweier,Olaf Rittinger,Ingrid Bader,Siren Berland,Trevor Cole,Franziska Degenhardt,Nataliya Di Donato,Luitgard Graul‐Neumann,Juliane Hoyer,Sally Ann Lynch,Ingrid Vlasak,Dagmar Wieczorek	2014	20
17	Evidence for anticipation in Beckwith–Wiedemann syndrome Siren Berland,Mia Appelbäck,Ove Bruland,Jasmin Beygo,Karin Buiting,Deborah Mackay,I. Karen Temple,Gunnar Houge	2013	22
18	Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA Patrick Edery,Charles Marcaillou,Mourad Sahbatou,Audrey Labalme,Joëlle Chastang,Renaud Touraine,Emmanuel Tubacher,Faiza Senni,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	2011	159
19	<i>PHF6</i> Deletions May Cause Borjeson-Forssman-Lehmann Syndrome in Females Siren Berland,K. Alme,A. Brendehaug,Gunnar Houge,Randi Hovland	2010	28
20	Late-onset gain of skills and peculiar jugular pit in an 11-year-old girl with 5q14.3 microdeletion including MEF2C Siren Berland,Gunnar Houge	2010	16

About Siren Berland

Siren Berland is a scholar working on Genetics, Immunology and Allergy and Gastroenterology, having authored 28 papers that have together received 478 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (4 papers), Retinal Development and Disorders (4 papers), Congenital Ear and Nasal Anomalies (3 papers), Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Genetics (207 citations), Molecular Biology (360 citations) and Ophthalmology (35 citations). Siren Berland has collaborated with scholars based in Norway, United Kingdom and Sweden. Frequent 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.

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