Eva‐Lena Stattin - Concepedia

Author

Eva‐Lena Stattin

Umeå University ORCID

Also Known As

Anna von Wachenfeldt, Carina Olofsson, E.-L. Stattin, Eva-Lena Stattin, Evalena Stattin, Eva‐Lena Stattin, Joakim Klar

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Umeå University Uppsala University Science for Life Laboratory Karolinska Institutet Hôpital Necker-Enfants Malades

About

Eva‐Lena Stattin is an author at Umeå University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	250
2	Cell Biology	2	2	41
3	Health Sciences	1	1	16
4	Biostatistics	1	1	25
5	Cellular Physiology	1	1	16

Eva‐Lena Stattin

Publications

951

Citations

H-Index

Page 1

	Year	Citations
Urinary albumin excretion rate and glomerular filtration rate in the prediction of diabetic nephropathy; a long‐term follow‐up study of childhood onset type‐1 diabetic patients Gisela Dahlquist, Eva‐Lena Stattin, Susanne Rudberg Nephrology Dialysis Transplantation	2001	105
Higher Intakes of Fish Protein Are Related to a Lower Risk of Microalbuminuria in Young Swedish Type 1 Diabetic Patients Anna Möllsten, Gisela Dahlquist, Eva‐Lena Stattin, Diabetes Care	2001	94
Celiprolol Treatment in Patients with Vascular Ehlers-Danlos Syndrome Hassan Baderkhan, Anders Wanhainen, A. Stenborg, European Journal of Vascular and Endovascular Surgery	2020	67
Genetic screening in sudden cardiac death in the young can save future lives Eva‐Lena Stattin, Ida Maria Westin, Kristina Cederquist, International Journal of Legal Medicine	2015	65
Familial osteochondritis dissecans associated with early osteoarthritis and disproportionate short stature Eva‐Lena Stattin, Yelverton Tegner, Magnus Domellöf, Osteoarthritis and Cartilage RheumatologyMusculoskeletal ResearchShort StatureFamilial Osteochondritis DissecansPathology	2008	61
Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11 Christian Wentzel, Evica Rajcan‐Separovic, Claudia Ruivenkamp, European Journal of Human Genetics Interstitial DeletionsMedicineGeneticsGenetic DisorderPathology	2011	60
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination Emma Hilton, Forbes Manson, Jill Urquhart, Human Molecular Genetics	2007	52
Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden Annika Winbo, Eva‐Lena Stattin, Ulla‐Britt Diamant, EP Europace	2012	44
A novel variant in MYLK causes thoracic aortic dissections: genotypic and phenotypic description Matias Hannuksela, Eva‐Lena Stattin, Joakim Klar, BMC Medical Genetics	2016	39
Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing Eva‐Lena Stattin, Ida Maria Boström, Annika Winbo, BMC Cardiovascular Disorders	2012	36

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