Ulla Bengtsson

2.1k citations

67 papers · 1.5k indexed · h-index 24

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
Urology top 5%

Papers in

Nephrology 7
Urology 6
- Urinary Bladder and Prostate Research 5

Co-authors: John J. Wasmuth Lennart Angervall Michael R. Altherr Sonny L. Johansson Sara T. Winokur Joan Overhauser Janet A. Warrington Christian Svalander
Journals: Human Molecular Genetics (3 papers)Genomics (3 papers)Genes Chromosomes and Cancer (3 papers)The Lancet (3 papers)QJM (2 papers)
Partner nations: Sweden United States United Kingdom

In The Last Decade

Ulla Bengtsson

64 papers receiving 1.4k citations

Peers

Countries citing papers authored by Ulla Bengtsson

Since Specialization

Citations

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

Fields of papers citing papers by Ulla Bengtsson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Clinical Standardization of the TRUE Test� Formaldehyde Patch Current problems in dermatology ·Torkel Fischer, Mourad Ben Amor Mohamed, Ulla Bengtsson, Peter J. Frosch, 美貴子中尾, Elisabetta Giuliana, Y. Lemaitre, S. Shaw, Max-Planck-Gesellschaft zur Förderung der Wissenschaften. Forschungsstelle Gottstein, John Wilkinson	2015	2
2	Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei European Journal of Human Genetics ·Mary Jean Roeder Gast, Franciszek K. Gtowka, Jessica C. de Greef, Ulla Bengtsson, Melanie Ehrlich, Rabi Tawil, Leslie F. Lock, Jane Hewitt, Jennifer Stocksdale, Jorge Martı́n, Silvère M. van der Maarel, Sara T. Winokur	2009	32
3	A functional investigation of tumor suppressor gene activities in a nasopharyngeal carcinoma cell line HONE1 using a monochromosome transfer approach Genes Chromosomes and Cancer ·Yue Cheng, Eric J. Stanbridge, Heidi H. Kong, Ulla Bengtsson, Michael I. Lerman, Maria Li Lung	2000	35
4	Characterization of the murine homolog of C1qRP: identical cellular expression pattern, chromosomal location and functional activity of the human and murine C1qRP Molecular Immunology ·Ruth DeFries, V. Makropoulos, Ronald R. Nepomuceno, Gail Palmarini, Sara T. Winokur, B. Juszczak, Ulla Bengtsson, Andrea J. Tenner	2000	19
5	Malignant transformation of human diploid fibroblasts and suppression of their anchorage independence by introduction of chromosome 13 Genes Chromosomes and Cancer ·Kiyomasa Oka, Pierre Perreault, Yu. V. Kosichkin, Haiyan Ge, Ulla Bengtsson, Eric J. Stanbridge, Naohisa Yoshioka, Qin Li, Akira Hakura, Masuo Yutsudo	1999	7
6	Analysis of aberrant methylation of the VHL gene by transgenes, monochromosome transfer, and cell fusion Oncogene ·Igor Kuzmin, L. Geil, Haiyan Ge, Ulla Bengtsson, Fuh-Mei Duh, Eric J. Stanbridge, Michael I. Lerman	1999	19
7	A NHE3-related pseudogene is on human Chromosome 10; the functional gene maps to 5pl5.3 Mammalian Genome ·Freddy Kokke, Tarek El-Sawy, Ulla Bengtsson, John J. Wasmuth, Ethylin Wang Jabs, Chung‐Ming Tse, Mark Donowitz, Steven R. Brant	1996	6
8	The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease Chromosome Research ·Sara T. Winokur, Ulla Bengtsson, Karina I. Torres, Katherine D. Mathews, Barbara Weiffenbach, Yupeng Zhou, Ana Julissa Naquiche Calero, C Packard, Jordanah M. Evans, Michael R. Altherr, Brian C. Schutte	1994	126
9	Genes encoding adrenergic receptors are not clustered on the long arm of human chromosome 5 Cytogenetic and Genome Research ·Stacie K. Loftus, Rita Shiang, Janet A. Warrington, Ulla Bengtsson, John D. McPherson, J.J. Wasmuth	1994	4
10	High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q Human Molecular Genetics ·Ulla Bengtsson, Michael R. Altherr, John J. Wasmuth, Sara T. Winokur	1994	25
11	High-Resolution Physical Mapping of Human 5q31-q33 Using Three Methods: Radiation Hybrid Mapping, Interphase Fluorescence in Situ Hybridization, and Pulsed-Field Gel Electrophoresis Genomics ·Janet A. Warrington, Ulla Bengtsson	1994	33
12	Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization American Journal of Medical Genetics ·Renée Bernstein, Maureen Bocian, Jonge Uribe Vergara, Ulla Bengtsson, John J. Wasmuth	1993	5
13	Assignment of the Cysteinyl-tRNA Synthetase Gene (CARS) to 11p15.5 Genomics ·T. A. Brzvstowski, Ulla Bengtsson, jeannette mcmahon, John J. Wasmuth, Stuart M. Arfin	1993	10
14	High resolution physical map of the region surrounding the spinal muscular atrophy gene Human Molecular Genetics ·Yong Yuan, Karen Morrison, Patrick W. Kleyn, Ulla Bengtsson, T. Conrad Gilliam, Kay E. Davies, John J. Wasmuth, John D. McPherson	1993	35
15	Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus. PubMed Central ·Barbara A. Smith, Douglas Skarecky, Ulla Bengtsson, R.E. Magenis, Nancy J. Carpenter, John J. Wasmuth	1988	80
16	Monoclonal IgG Cryoglobulinemia with Secondary Development of Glomerulonephritis and Nephrotic Syndrome QJM ·Ulla Bengtsson, R. K. Naitam, Göran Lindstedt, Christian Svalander	1975	26
17	PHENACETIN-CONTAINING ANALGESICS AND CHRONIC RENAL DISEASE The Lancet ·Ulla Bengtsson	1975	4
18	Phenacetin abuse and renal pelvic carcinoma. PubMed ·Ulla Bengtsson, Lennart Angervall, S. Johansson, Xiaoting Xi	1975	6
19	Phenacetin and renal pelvic carcinoma. PubMed ·Ulla Bengtsson	1974	8
20	Intensive Treatment of Chronic Pyelonephritis Acta Medica Scandinavica ·B. Hood, Ulla Bengtsson, B. Isaksson, H. Calvillo, C. Rådberg	1960	6

About Ulla Bengtsson

Ulla Bengtsson is a scholar working on Nephrology, Urology, Pediatrics, Perinatology and Child Health, Rheumatology and Gastroenterology, having authored 67 papers that have together received 1.5k indexed citations. Recurring topics across this work include Pediatric Urology and Nephrology Studies (11 papers), Urinary Tract Infections Management (8 papers), RNA modifications and cancer (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Urinary Bladder and Prostate Research (5 papers), Prenatal Screening and Diagnostics (5 papers), Muscle Physiology and Disorders (4 papers) and Kidney Stones and Urolithiasis Treatments (4 papers). The work is most often cited by research in Genetics (175 citations), Genetics (421 citations), Urology (80 citations), Pharmacology (104 citations) and Nephrology (83 citations). Ulla Bengtsson has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include John J. Wasmuth, Lennart Angervall, Michael R. Altherr, Sonny L. Johansson, Sara T. Winokur, Joan Overhauser, Janet A. Warrington, Christian Svalander, Eric J. Stanbridge and Deanna M. Church. Their work appears in journals such as Human Molecular Genetics, Genomics, Genes Chromosomes and Cancer, The Lancet and QJM.

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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