Ola Sandgren

2.6k citations

49 papers · 2.0k indexed · 1 hit paper · h-index 23

Impact in

Ophthalmology top 0.5%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
Molecular Biology top 5%
- Retinal Development and Disorders
- Amyloidosis: Diagnosis, Treatment, Outcomes

Papers in

Ophthalmology 13
- Retinal Diseases and Treatments 11
- Glaucoma and retinal disorders 4
Molecular Biology 44
- Retinal Development and Disorders 23
- Amyloidosis: Diagnosis, Treatment, Outcomes 18

Co-authors: Gösta Holmgren Marie Burstedt Irina Golovleva Sten Andréasson Kristina Forsman‐Semb Claes Wadelius Ulf Drugge Konstantin Petrukhin
Journals: Acta Ophthalmologica (5 papers)Amyloid (4 papers)European Journal of Human Genetics (3 papers)Ophthalmic Genetics (3 papers)Advances in experimental medicine and biology (3 papers)
Partner nations: Sweden United States Japan

In The Last Decade

Ola Sandgren

49 papers receiving 2.0k citations

Hit Papers

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Identification of the gene responsible for Best macular dystrophy 1998 · 541 citations

Peers

Countries citing papers authored by Ola Sandgren

Since Specialization

Citations

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

Fields of papers citing papers by Ola Sandgren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Genetic Heterogeneity and Clinical Outcome in a Swedish Family with Retinal Degeneration Caused by Mutations in CRB1 and ABCA4 Genes Advances in experimental medicine and biology ·Frida Jönsson, Marie Burstedt, Ola Sandgren, Anna Norberg, Irina Golovleva	2014	3
2	Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family European Journal of Human Genetics ·Frida Jönsson, Marie Burstedt, Ola Sandgren, Anna Norberg, Irina Golovleva	2013	17
3	Mutation Spectra in Autosomal Dominant and Recessive Retinitis Pigmentosa in Northern Sweden Advances in experimental medicine and biology ·Irina Golovleva, Linda M. Kohn, Marie Burstedt, Stephen P. Daiger, Ola Sandgren	2009	14
4	Ocular manifestations in liver transplant recipients with familial amyloid polyneuropathy Acta Ophthalmologica ·Ola Sandgren, Daniel Kjellgren, Ole B. Suhr	2008	48
5	Mutation in the PYK2-Binding Domain of PITPNM3 Causes Autosomal Dominant Cone Dystrophy (CORD5) in Two Swedish Families Advances in experimental medicine and biology ·Linda M. Kohn, Inova Lee, Marie Burstedt, Š. Piskoř, Ola Sandgren, Irina Golovleva	2007	5
6	Tinted contact lenses in Bothnia dystrophy Acta Ophthalmologica Scandinavica ·Alexandra Geraseva, Marie Burstedt, Irina Golovleva, Ola Sandgren	2007	4
7	A Molecular Model of the Amyloid Fibril Novartis Foundation symposium ·Colin Blake, Louise C. Serpell, Margaret Sunde, Ola Sandgren, Erik Lundgren	2007	12
8	ASSOCIATIONS BETWEEN SPECIFIC MEASURES OF VISION AND VISION-RELATED QUALITY OF LIFE IN PATIENTS WITH BOTHNIA DYSTROPHY, A DEFINED TYPE OF RETINITIS PIGMENTOSA Retina ·Marie Burstedt, Eva Mönestam, Ola Sandgren	2005	30
9	Retinal function in Bothnia dystrophy. An electrophysiological study Vision Research ·Marie Burstedt, Ola Sandgren, Irina Golovleva, Lillemor Wachtmeister	2003	21
10	Enhancement of AA-amyloid formation in mice by transthyretin amyloid fragments and polyethylene glycol Biochimica et Biophysica Acta (BBA) - General Subjects ·Sanghyuk Choi, Yukio Ando, Intissar Anan, Gösta Holmgren, Ola Sandgren, Sergey Tychina, Kazuhiro Tashima, Ole B. Suhr	2000	10
11	Identification of the gene responsible for Best macular dystrophy Nature Genetics ·Konstantin Petrukhin, 遠峰洋, Benjamin Bakall, Wen Li, Guochun Xie, 程路平, Ola Sandgren, Kristina Forsman, Gösta Holmgren, Sten Andréasson, Mihailo Vujic, Arthur A. Bergen, Lopez Aguayo Mari Carmen, David J. Figueroa, Christopher P. Austin, Michael L. Metzker, C. Thomas Caskey, Claes Wadelius Hit paper breakdown →	1998	541
12	Angioid streaks are part of a familial syndrome of dyserythropoietic anaemia (CDA III) British Journal of Haematology ·Herbert Sandström, Anders Wåhlin, Mikael Eriksson, Gösta Holmgren, C.H.Lee, Ola Sandgren	1997	20
13	Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids Human Genetics ·Caroline Graff, Anna Eriksson, Kristina Forsman, Ola Sandgren, Matthew F. Webb, Claes Wadelius	1997	11
14	A New Simple and Rapid Screening Method for Variant Transthyretin-Related Amyloidosis Biochemical and Biophysical Research Communications ·Yukio Ando, Per‐Ingvar Ohlsson, Ole B. Suhr, Nils Nyhlin, Taro Yamashita, Gösta Holmgren, Åke Danielsson, Ola Sandgren, Makoto Uchino, Masayuki Ando	1996	61
15	Ocular amyloidosis, with special reference to thehereditary forms with vitreous involvement Survey of Ophthalmology ·Ola Sandgren	1995	87
16	A Gene for Autosomal Dominant Progressive Cone Dystrophy (CORD5) Maps to Chromosome 17p12–p13 Genomics ·Jorune Balciuniene, H Czembirek, Ola Sandgren, Lillemor Wachtmeister, Gösta Holmgren, Liyou Chen	1995	62
17	Fine Mapping of Best's Macular Dystrophy Localizes the Gene in Close Proximity to but Distinct from the D11S480/ROM1 Loci Genomics ·Caroline Graff, Kristina Forsman, Jianfan Lu, Stefan Nordström, Lisbet K. Lind, H Czembirek, Ola Sandgren, Jean Weissenbach, Gösta Holmgren, Karl‐Henrik Gustavson, Claes Wadelius	1994	18
18	Vitreous Amyloidosis Associated With Homozygosity for the Transthyretin Methionine-30 Gene Archives of Ophthalmology ·Ola Sandgren	1990	25
19	Conjunctival involvement in familial amyloidotic polyneuropathy Acta Ophthalmologica ·Ola Sandgren, Ufairah Ariqah Heru	1990	3
20	Relation of Vitreous Amyloidosis to Prealbumin Ophthalmic Research ·Ola Sandgren, Per Westermark, Jung Kwon Lee	1986	15

About Ola Sandgren

Ola Sandgren is a scholar working on Ophthalmology, Molecular Biology, Cell Biology, Genetics and Physiology, having authored 49 papers that have together received 2.0k indexed citations. Recurring topics across this work include Retinal Development and Disorders (23 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (18 papers), Retinal Diseases and Treatments (11 papers), Dermatological and Skeletal Disorders (9 papers), Alzheimer's disease research and treatments (7 papers), Cellular transport and secretion (5 papers), Trace Elements in Health (4 papers) and Glaucoma and retinal disorders (4 papers). The work is most often cited by research in Ophthalmology (696 citations), Molecular Biology (1.8k citations), Cell Biology (345 citations), Cellular and Molecular Neuroscience (325 citations) and Genetics (259 citations). Ola Sandgren has collaborated with scholars based in Sweden, United States and Japan. Frequent co-authors include Gösta Holmgren, Marie Burstedt, Irina Golovleva, Sten Andréasson, Kristina Forsman‐Semb, Claes Wadelius, Ulf Drugge, Konstantin Petrukhin, Wen Li and Benjamin Bakall. Their work appears in journals such as Acta Ophthalmologica, Amyloid, European Journal of Human Genetics, Ophthalmic Genetics and Advances in experimental medicine and biology.

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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