Ulla Grandell

789 total citations
11 papers, 465 citations indexed

About

Ulla Grandell is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Ulla Grandell has authored 11 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Ulla Grandell's work include Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (3 papers) and Hormonal and reproductive studies (2 papers). Ulla Grandell is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (3 papers) and Hormonal and reproductive studies (2 papers). Ulla Grandell collaborates with scholars based in Sweden, United Kingdom and United States. Ulla Grandell's co-authors include Maria Anvret, Lars Edström, Birgitta Hedberg, Gunnel Ahlberg, Keith Johnson, Göran Toss, Britt Skogseid, Magnus Nordenskjöld, Eva Lindgren and Emma Tham and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Human Molecular Genetics.

In The Last Decade

Ulla Grandell

11 papers receiving 454 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ulla Grandell Sweden	8	337	307	170	78	66	11	465
Ulf Drugge Sweden	11	328 1.0×	89 0.3×	118 0.7×	23 0.3×	96 1.5×	26	501
Ana L. Pelayo‐Negro Spain	13	164 0.5×	304 1.0×	181 1.1×	21 0.3×	26 0.4×	27	450
Sheng Yao China	12	253 0.8×	184 0.6×	118 0.7×	13 0.2×	58 0.9×	33	434
Qingwen Xia Canada	7	309 0.9×	138 0.4×	43 0.3×	10 0.1×	45 0.7×	9	400
Yusaku Shimizu Japan	8	203 0.6×	110 0.4×	51 0.3×	21 0.3×	31 0.5×	21	266
John E. Antoine France	10	92 0.3×	147 0.5×	496 2.9×	62 0.8×	69 1.0×	20	579
Marie‐Laure Martin‐Négrier France	12	178 0.5×	73 0.2×	85 0.5×	15 0.2×	22 0.3×	22	305
Nedim Hukovic Canada	6	231 0.7×	108 0.4×	66 0.4×	251 3.2×	16 0.2×	8	437
Philip A. Wilkinson United Kingdom	8	71 0.2×	183 0.6×	67 0.4×	20 0.3×	15 0.2×	9	311
Saori Morozumi Japan	9	65 0.2×	87 0.3×	202 1.2×	24 0.3×	13 0.2×	17	330

Countries citing papers authored by Ulla Grandell

Since Specialization

Citations

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

Fields of papers citing papers by Ulla Grandell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulla Grandell

This figure shows the co-authorship network connecting the top 25 collaborators of Ulla Grandell. A scholar is included among the top collaborators of Ulla Grandell 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 Ulla Grandell. Ulla Grandell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Omrani, Mir Davood, et al.. (2011). 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in Three Adult Iranian Siblings. Sexual Development. 5(6). 273–276. 10 indexed citations

Tham, Emma, Ulla Grandell, Eva Lindgren, et al.. (2007). Clinical Testing for Mutations in theMEN1Gene in Sweden: A Report on 200 Unrelated Cases. The Journal of Clinical Endocrinology & Metabolism. 92(9). 3389–3395. 81 indexed citations

Giwercman, Yvonne Lundberg, Agneta Nordenskjöld, E. Martin Ritzén, et al.. (2002). An Androgen Receptor Gene Mutation (E653K) in a Family with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency as well as in Partial Androgen Insensitivity. The Journal of Clinical Endocrinology & Metabolism. 87(6). 2623–2628. 16 indexed citations

Bui, The‐Hung, et al.. (2000). Early prenatal diagnosis of the ICF syndrome. Prenatal Diagnosis. 20(10). 828–831. 5 indexed citations

Lindgren, AC, Ulla Grandell, E. Martin Ritzén, & Maria Anvret. (1996). Diagnosis of the Prader‐Willi syndrome by proving the absence of the unmethylated PW71 DNA fragment. Acta Paediatrica. 85(2). 195–198. 10 indexed citations

Telenius, H., E. Almqvist, B Kremer, et al.. (1995). Somatic mosaicism in sperm is associated with intergenerational (CAG)_n changes in Huntington disease. Human Molecular Genetics. 4(2). 189–195. 67 indexed citations

Carey, Nessa, Keith Johnson, Pekka Nokelainen, et al.. (1995). Reply to “Meiotic drive and myotonic dystrophy”. Nature Genetics. 10(2). 133–133. 3 indexed citations

Almqvist, E., Susan E. Andrew, Jane Theilmann, et al.. (1994). Geographical distribution of haplotypes in Swedish families with Huntington's disease. Human Genetics. 94(2). 124–8. 8 indexed citations

Ashizawa, Tetsuo, Maria Anvret, Montserrat Baiget, et al.. (1994). Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.. PubMed. 54(3). 414–23. 99 indexed citations

10.

Dahl, Niklas, Ulla Grandell, Tommy Martinsson, et al.. (1993). Frequency of four cystic fibrosis mutations in a Swedish population. Acta Paediatrica. 82(6-7). 609–609. 7 indexed citations

11.

Anvret, Maria, Gunnel Ahlberg, Ulla Grandell, et al.. (1993). Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy. Human Molecular Genetics. 2(9). 1397–1400. 159 indexed citations

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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