Eva Holmberg

2.9k citations

40 papers · 1.5k indexed · h-index 22

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
Molecular Biology
- RNA modifications and cancer

Papers in

Animal Science and Zoology 9
- Pharmacological Effects and Assays 8
Genetics 18
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 3
- Diabetes and associated disorders 3

Co-authors: Bertil Waldeck Ulf Kristoffersson Magnus Nordenskjöld Göran Annerén Elisabeth Blennow Åke Lernmark Ingrid Kockum Ralf Waßmuth
Journals: Clinical Genetics (4 papers)Orphanet Journal of Rare Diseases (1 paper)European Journal of Human Genetics (1 paper)Prenatal Diagnosis (1 paper)Hereditas (1 paper)
Partner nations: Sweden United States Belgium

In The Last Decade

Eva Holmberg

39 papers receiving 1.4k citations

Peers

Countries citing papers authored by Eva Holmberg

Since Specialization

Citations

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

Fields of papers citing papers by Eva Holmberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Repeated allopregnanolone exposure induces weight gain in schedule fed rats on high fat diet Physiology & Behavior ·Eva Holmberg, Maja Johansson, Torbjörn Bäckström, Mats Löfgren, David Haage	2014	11
2	Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome Orphanet Journal of Rare Diseases ·Fransiska Malfait, Sofie Symoens, Nathalie Goemans, Yolanda Gyftodimou, Eva Holmberg, Vanesa López‐González, Geert Mortier, Sheela Nampoothiri, Michael B. Petersen, Anne De Paepe	2013	62
3	Phenotype and natural history in Marshall–Smith syndrome American Journal of Medical Genetics Part A ·Adam Shaw, Dunya Omer Kareem, Mislen Bauer, Trevor Cole, Marie‐Ange Delrue, Arie van Haeringen, Eva Holmberg, Samantha J.L. Knight, Geert Mortier, Sheela Nampoothiri, Silvija Pušeljić, Martin Zenker, Valérie Cormier‐Daire, Raoul C. M. Hennekam	2010	29
4	A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population American Journal of Medical Genetics Part A ·Miriam Entesarian, Birgit Carlsson, Mahmoud Mansouri, Eva‐Lena Stattin, Eva Holmberg, Irina Golovleva, Hreinn Stefánsson, Joakim Klar, Niklas Dahl	2009	11
5	Genetic differences in nutritional performance of some specific pathogen-free mice strains Hereditas ·Eva Holmberg, Ivan Kreft, L. Munck	2009	1
6	SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·W W Chen, Atle Melberg, Raili Raininko, Eva Kumlien, Miriam Entesarian, Per G. Söderberg, Dr D.S. Bebincy, Niklas Darín, Mårten Kyllerman, Eva Holmberg, Henry Engler, Urban Eriksson, Niklas Dahl	2009	40
7	Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disorders Journal of Medical Genetics ·Сулейманова Олеся Анатольевна, Sara Ekvall, 代金平, Maria Björkqvist, Geir J. Braathen, Karel Duchén, S Achmad Jaka, Eva Holmberg, Paul Amuna, Néstor A. Peralta-Zapata, Göran Annerén, Amr A. Youssef	2008	63
8	CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome Clinical Genetics ·Josephine Wincent, Eva Holmberg, Kerstin Strömland, Maria Soller, Gregor Brück, Tatjana Djureinovic, Enas Mushtaq, Carlos Alberto Bejarano Martínez, Jacqueline Schoumans	2008	46
9	Identification of Genomic Deletions of the APC Gene in Familial Adenomatous Polyposis by Two Independent Quantitative Techniques Genetic Testing ·Johan Meuller, Gunilla Kanter-Smoler, Anders O.H. Nygren, Abdellatif Errami, Henrik Grönberg, Eva Holmberg, Jan Björk, Jan Wahlström, Margareta Nordling	2004	20
10	Genome-wide screening using array-CGH does not reveal microdeletions/microduplications in children with Kabuki syndrome European Journal of Human Genetics ·Jacqueline Schoumans, Ann Nordgren, Claudia Ruivenkamp, Karen Brøndum‐Nielsen, Bin Tean Teh, Göran Annerén, Eva Holmberg, Magnus Nordenskjöld, Britt-Marie Anderlid	2004	23
11	A family with pyruvate dehydrogenase complex deficiency due to a novel C>T substitution at nucleotide position 407 in exon 4 of the X-linked Ε1α gene European Journal of Pediatrics ·M. Tulinius, Niklas Darín, Lars‐Martin Wiklund, Eva Holmberg, Jan Erik Eriksson, Willy Lissens, Linda De Meırleır, Elisabeth Holme	2004	11
12	Detailed characterization of 12 supernumerary ring chromosomes using micro‐FISH and search for uniparental disomy American Journal of Medical Genetics ·Britt‐Marie Anderlid, Sigrid Sahlén, Jacqueline Schoumans, Eva Holmberg, Linda Fägersten, Geert Mortier, Frank Speleman, Elisabeth Blennow	2001	64
13	DGGE screening of mutations in mismatch repair genes (hMSH2 and hMLH1) in 34 Swedish families with colorectal cancer Clinical Genetics ·Erika Sieder, Siobhan Wahlberg, Carlos Rubio-Terrés, Eva Holmberg, Hsiang-An Yang, Annika Lindblom	1998	23
14	De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring Human Genetics ·Shabalyn, Massoud Houshmand, Nils‐Göran Larsson, Elisabeth Holme, Anders Oldfors, Eva Holmberg, Isidore Fleisher	1995	30
15	Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization American Journal of Medical Genetics ·Shafina Fatima Almatisha, Karen Brøndum Nielsen, Håkan Telenius, Novia Hanasti, Ulf Kristoffersson, Eva Holmberg, Christopher Gillberg, Magnus Nordenskjöld	1995	96
16	Inheritance of MHC class II genes in IDDM studied in population-based affected and control families Diabetologia ·Ingrid Kockum, Ralf Waßmuth, Eva Holmberg, B Michelsen, Åke Lernmark	1994	13
17	Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization Prenatal Diagnosis ·Elisabeth Blennow, The‐Hung Bui, Ulf Kristoffersson, Mihailo Vujic, Göran Annerén, Eva Holmberg, Magnus Nordenskjöld	1994	91
18	HLA DR AND DQ RFLP ANALYSIS IN CROHN'S DISEASE International Journal of Immunogenetics ·Ralf Waßmuth, Susan Eastman, Ingrid Kockum, Eva Holmberg, Marianne Starck, T. Lindhagen, Joachim R. Kalden, Åke Lernmark, G. Sundkvist, Stefan Lindgren	1993	4
19	Association of the Robin sequence with the fragile X syndrome American Journal of Medical Genetics ·Ave M. Lachiewicz, Hu ChaoXing, Gösta Holmgren, Eva Holmberg, Fas G B Ogunmola	1991	6
20	Pentobarbitone and skeletal muscle contractions: on the interaction with the effect elicited by the β-adrenoceptor agonist, terbutaline Journal of Pharmacy and Pharmacology ·Eva Holmberg, Bertil Waldeck	1979	5

About Eva Holmberg

Eva Holmberg is a scholar working on Animal Science and Zoology, Genetics, Developmental Biology, Genetics and Clinical Biochemistry, having authored 40 papers that have together received 1.5k indexed citations. Recurring topics across this work include Pharmacological Effects and Assays (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (3 papers), Diabetes and associated disorders (3 papers), Peptidase Inhibition and Analysis (3 papers), Cancer Genomics and Diagnostics (3 papers), Pain Mechanisms and Treatments (3 papers) and Genetic factors in colorectal cancer (3 papers). The work is most often cited by research in Genetics (685 citations), Genetics (174 citations), Molecular Biology (680 citations), Oncology (243 citations) and Pediatrics, Perinatology and Child Health (164 citations). Eva Holmberg has collaborated with scholars based in Sweden, United States and Belgium. Frequent co-authors include Bertil Waldeck, Ulf Kristoffersson, Magnus Nordenskjöld, Göran Annerén, Elisabeth Blennow, Åke Lernmark, Ingrid Kockum, Ralf Waßmuth, B Michelsen and Jacqueline Schoumans. Their work appears in journals such as Clinical Genetics, Orphanet Journal of Rare Diseases, European Journal of Human Genetics, Prenatal Diagnosis and Hereditas.

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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