Astrīda Krūmiņa

1.8k total citations
27 papers, 337 citations indexed

About

Astrīda Krūmiņa is a scholar working on Genetics, Molecular Biology and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Astrīda Krūmiņa has authored 27 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Molecular Biology and 3 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Astrīda Krūmiņa's work include Craniofacial Disorders and Treatments (7 papers), Cleft Lip and Palate Research (7 papers) and Forensic and Genetic Research (6 papers). Astrīda Krūmiņa is often cited by papers focused on Craniofacial Disorders and Treatments (7 papers), Cleft Lip and Palate Research (7 papers) and Forensic and Genetic Research (6 papers). Astrīda Krūmiņa collaborates with scholars based in Latvia, Estonia and Lithuania. Astrīda Krūmiņa's co-authors include Baiba Lāce, Vaidutis Kučinskas, Aavo‐Valdur Mikelsaar, G. Beckman, Liāna Pliss, Viesturs Baumanis, L. Beckman, Matthew E. Hurles, Chris Tyler‐Smith and Tatiana Zerjal and has published in prestigious journals such as Journal of Neurology Neurosurgery & Psychiatry, Molecular Biology and Evolution and Experimental Gerontology.

In The Last Decade

Astrīda Krūmiņa

27 papers receiving 320 citations

Peers

Countries citing papers authored by Astrīda Krūmiņa

Since Specialization

Citations

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

Fields of papers citing papers by Astrīda Krūmiņa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrīda Krūmiņa

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Population Genetics of Latvians in the Context of Admixture between North-Eastern European Ethnic Groups 2018 ·Proceedings of the Latvian Academy of Sciences Section B Natural Exact and Applied Sciences ·Astrīda Krūmiņa, Liāna Pliss, Gunita Zariņa, (unknown), (unknown), Baiba Lāce, Didzis Elferts, Andrey Khrunin, Limborskaia Sa, Jānis Kloviņš, Linda Gailīte	3
2	Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease 2017 ·Molecular Genetics & Genomic Medicine ·(unknown), Ieva Tolmane, (unknown), (unknown), (unknown), (unknown), Ieva Mičule, Zita Krūmiņa, Astrīda Krūmiņa, Baiba Rozentāle, Linda Gailīte	4
3	Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies 2016 ·BMC Musculoskeletal Disorders ·Inna Inashkina, Eriks Jankevics, (unknown), (unknown), (unknown), Ieva Mičule, Jurģis Strautmanis, (unknown), Loreta Cimbalistienė, Vaidutis Kučinskas, Astrīda Krūmiņa, Algirdas Utkus, Birutė Burnytė, Aušra Matulevičienė, Baiba Lāce	8
4	A New Baltic Population-Specific Human Genetic Marker in the PMCA4 Gene 2016 ·Human Heredity ·(unknown), Inna Inashkina, Baiba Lāce, (unknown), Limborskaia Sa, Andrey Khrunin, Vaidutis Kučinskas, Astrīda Krūmiņa, Linda Gailīte, Branko Zorn, (unknown), Margus Punab, Juris Ērenpreiss	1
5	Comparison of telomere length between population-specific mitochondrial haplogroups among different age groups in a Latvian population 2015 ·Mechanisms of Ageing and Development ·(unknown), Didzis Elferts, (unknown), Astrīda Krūmiņa, (unknown), (unknown), Renāte Ranka, Liāna Pliss	3
6	Y‐Chromosomal Lineages of Latvians in the Context of the Genetic Variation of the Eastern‐Baltic Region 2015 ·Annals of Human Genetics ·Liāna Pliss, (unknown), Siiri Rootsi, Kristiina Tambets, (unknown), (unknown), (unknown), (unknown), (unknown), Baiba Lāce, Vaidutis Kučinskas, Astrīda Krūmiņa, Renāte Ranka, Viesturs Baumanis	11
7	Dynamics of Telomere Length in Different Age Groups in a Latvian Population 2013 ·Current Aging Science ·(unknown), Liāna Pliss, Renāte Ranka, Astrīda Krūmiņa, Viesturs Baumanis	7
8	The link between mitochondrial DNA hypervariable segment I heteroplasmy and ageing among genetically unrelated Latvians 2011 ·Experimental Gerontology ·Liāna Pliss, (unknown), Renāte Ranka, Didzis Elferts, Astrīda Krūmiņa, Viesturs Baumanis	5
9	Association studies of candidate genes and cleft lip and palate taking into consideration geographical origin 2011 ·European Journal Of Oral Sciences ·Baiba Lāce, (unknown), Linda Gailīte, (unknown), Jānis Kloviņš, Liāna Pliss, Astrīda Krūmiņa, Alexandre R. Vieira	7
10	Variation in FGF1, FOXE1, and TIMP2genes is associated with nonsyndromic cleft lip with or without cleft palate 2011 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Tiit Nikopensius, (unknown), Laima Ambrozaitytė, Triin Jagomägi, Mare Saag, Aušra Matulevičienė, Algirdas Utkus, Kaarel Krjutškov, (unknown), Linda Gailīte, Ilze Akota, (unknown), Astrīda Krūmiņa, Jānis Kloviņš, Baiba Lāce, Vaidutis Kučinskas, Andres Metspalu	38
11	Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate 2010 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Tiit Nikopensius, Triin Jagomägi, Kaarel Krjutškov, (unknown), Mare Saag, (unknown), Linda Gailīte, Ilze Akota, (unknown), Astrīda Krūmiņa, Laima Ambrozaitytė, Aušra Matulevičienė, Zita Aušrelė Kučinskienė, Baiba Lāce, Vaidutis Kučinskas, Andres Metspalu	37
12	Mitochondrial DNA origins of the Latvian clefting population 2010 ·Mitochondrion ·Alexandre R. Vieira, Liāna Pliss, (unknown), Astrīda Krūmiņa, Viesturs Baumanis, Baiba Lāce	3
13	Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss 2009 ·Proceedings of the Latvian Academy of Sciences Section B Natural Exact and Applied Sciences ·(unknown), (unknown), (unknown), (unknown), Astrīda Krūmiņa, (unknown), Aigars Pētersons	1
14	Age of SERPINA1 Gene PI Z Mutation: Swedish and Latvian Population Analysis 2008 ·Annals of Human Genetics ·Baiba Lāce, Tomas Sveger, (unknown), (unknown), Astrīda Krūmiņa	18
15	Mitochondrial DNA Portrait of Latvians: Towards the Understanding of the Genetic Structure of Baltic‐Speaking Populations 2006 ·Annals of Human Genetics ·Liāna Pliss, Kristiina Tambets, (unknown), (unknown), (unknown), Astrīda Krūmiņa, Viesturs Baumanis, Richard Villems	41
16	Diphtheria with polyneuropathy in a closed community despite receiving recent booster vaccination 2005 ·Journal of Neurology Neurosurgery & Psychiatry ·Astrīda Krūmiņa	14
17	Mitochondrial DNA Portrait of Latvians: Towards the Understanding of the Genetic Structure of Baltic-Speaking Populations 2005 ·Annals of Human Genetics ·Liāna Pliss, Kristiina Tambets, (unknown), (unknown), (unknown), Astrīda Krūmiņa, Viesturs Baumanis, Richard Villems	1
18	Geographical, Linguistic, and Cultural Influences on Genetic Diversity: Y-Chromosomal Distribution in Northern European Populations 2001 ·Molecular Biology and Evolution ·Tatiana Zerjal, L. Beckman, G. Beckman, Aavo‐Valdur Mikelsaar, Astrīda Krūmiņa, Vaidutis Kučinskas, Matthew E. Hurles, Chris Tyler‐Smith	62
19	α<sub>1</sub>-Antitrypsin (PI) Alleles as Markers of Westeuropean Influence in the Baltic Sea Region 1999 ·Human Heredity ·L. Beckman, (unknown), Aavo‐Valdur Mikelsaar, Astrīda Krūmiņa, Vaidutis Kučinskas, G. Beckman	13
20	Transferrin Variants as Markers of Migrations and Admixture between Populations in the Baltic Sea Region 1998 ·Human Heredity ·L. Beckman, (unknown), Aavo‐Valdur Mikelsaar, Astrīda Krūmiņa, (unknown), (unknown), G. Beckman	12

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.

Explore authors with similar magnitude of impact