🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Ann Nordgren

Karolinska University Hospital

ORCID: 0000-0003-3285-4281

Also affiliated with Sahlgrenska University Hospital, Karolinska Institutet, University of Gothenburg

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 9 papers. Top paper: “Implementing precision medicine in a regionally organized healthcare system in Sweden”.

Implementing precision medicine in a regionally organized healthcare system in Sweden

Nature Medicine(2022)10.1038/s41591-022-01963-4
N/A
0.568DataRank · unranked
43 citations

Valtteri Wirta, Lucia Cavelier, Eva Berglund, Mikaela Friedman, Michael Akhras +38 more

International Undiagnosed Diseases Programs (UDPs): components and outcomes

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-023-02966-1
N/A
0.406DataRank · unranked
14 citations

Lisa Ewans, Ryan Pysar, Fulya Taylan, Lorenzo D. Botto, Ann Nordgren +3 more

Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps

Genome Research(2024)10.1101/gr.279346.124
N/A
0.396DataRank · unranked
13 citations

Jesper Eisfeldt, Jesse D. Bengtsson, Ming Yin Lun, Christopher M. Grochowski, Medhat Mahmoud +17 more

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Nature Communications(2020)10.1038/s41467-020-18723-y
N/A
0DataRank · unranked
217 citations

Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe +95 more

Identification of biallelic POLA2 variants in two families with an autosomal recessive telomere biology disorder

European Journal of Human Genetics(2024)10.1038/s41431-024-01722-8
N/A
0DataRank · unranked
11 citations

Maria Pettersson, Pattra Chun‐on, Maryam Rafati, Lisa J. McReynolds, Anna Norberg +13 more

Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversions

medRxiv(2024)10.1101/2024.04.22.24305780
N/A
0DataRank · unranked
1 citations

Jesper Eisfeldt, Jesse D. Bengtsson, Ming Yin Lun, Christopher M. Grochowski, Medhat Mahmoud +14 more

Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta

Genetics in Medicine(2023)10.1016/j.gim.2023.100856
N/A
0DataRank · unranked
9 citations

Nicolas Chassaing, Nicola Ragge, Felix Boschann, Angelina My-Hoa Ngu, Elisabeth Meloche +49 more

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00870-6
N/A
0DataRank · unranked
117 citations

Tianyun Wang, Kendra Hoekzema, Jill A. Rosenfeld, Pengfei Liu, Hui Guo +95 more

Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

npj Genomic Medicine(2022)10.1038/s41525-021-00273-x
N/A
0DataRank · unranked
26 citations

Shuyang Zhang, Sigrún Hallgrímsdóttir, Yuzhi Zuo, Xiaoxin Li, Dominyka Batkovskyte +31 more