Baiba Lāce

1.0k total citations
50 papers, 474 citations indexed

About

Baiba Lāce is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Baiba Lāce has authored 50 papers receiving a total of 474 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 23 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Baiba Lāce's work include Cleft Lip and Palate Research (13 papers), Craniofacial Disorders and Treatments (12 papers) and Mitochondrial Function and Pathology (7 papers). Baiba Lāce is often cited by papers focused on Cleft Lip and Palate Research (13 papers), Craniofacial Disorders and Treatments (12 papers) and Mitochondrial Function and Pathology (7 papers). Baiba Lāce collaborates with scholars based in Latvia, United States and Canada. Baiba Lāce's co-authors include Alexandre R. Vieira, Astrīda Krūmiņa, Ilze Akota, Linda Gailīte, Inna Inashkina, Laima Ambrozaitytė, Dmitrijs Rots, Aušra Matulevičienė, Vaidutis Kučinskas and Mare Saag and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Annals of Neurology.

In The Last Decade

Baiba Lāce

47 papers receiving 460 citations

Peers

Baiba Lāce

GENET

RHEUM

ONCOL

Jodi D. Hoffman United States

Siham Chafai Elalaoui Morocco

Katherine Neas New Zealand

Pietro Sirleto Italy

Kristen Deak United States

Vanesa López‐González Spain

Güven Toksoy Türkiye

Shagun Aggarwal India

Philip N. Mowrey United States

Alper Gezdirici Türkiye

Jodi D. Hoffman United States

Baiba Lāce

365 ×1.5

GENET

215 ×1.0

41 ×0.7

GENET

35 ×1.0

RHEUM

23 ×0.7

ONCOL

Citations per year, relative to Baiba Lāce Baiba Lāce (= 1×) peers Jodi D. Hoffman

Countries citing papers authored by Baiba Lāce

Since Specialization

Citations

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

Fields of papers citing papers by Baiba Lāce

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Baiba Lāce

This figure shows the co-authorship network connecting the top 25 collaborators of Baiba Lāce. A scholar is included among the top collaborators of Baiba Lāce 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 Baiba Lāce. Baiba Lāce 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

Lāce, Baiba, et al.. (2025). Genetic Analysis of CYP1B1 and Other Anterior Segment Dysgenesis-Associated Genes in Latvian Cohort of Primary Congenital Glaucoma. Biomedicines. 13(5). 1222–1222.

Mičule, Ieva, et al.. (2024). Altered Splicing of LAMP2 in a Multigenerational Family from Latvia Affected by Danon Disease. Medicina. 60(1). 99–99. 1 indexed citations

Zayakin, Pawel, Marina Makrecka‐Kuka, Baiba Lāce, et al.. (2023). Impact of the m.13513G>A Variant on the Functions of the OXPHOS System and Cell Retrograde Signaling. Current Issues in Molecular Biology. 45(3). 1794–1809. 2 indexed citations

Rots, Dmitrijs, et al.. (2023). The most common European HINT1 neuropathy variant phenotype and its case studies. Frontiers in Neurology. 14. 1084335–1084335. 1 indexed citations

Laflamme, Nathalie, Baiba Lāce, Yvan Labrie, et al.. (2021). A Homozygous Deep Intronic Mutation Alters the Splicing of Nebulin Gene in a Patient With Nemaline Myopathy. Frontiers in Neurology. 12. 660113–660113. 6 indexed citations

Mičule, Ieva, Nathan T. Wright, Volker Straub, et al.. (2020). Collagen VI-related limb-girdle syndrome caused by frequent mutation in COL6A3 gene with conflicting reports of pathogenicity. Neuromuscular Disorders. 30(6). 483–491. 4 indexed citations

Picher‐Martel, Vincent, Yvan Labrie, Serge Rivest, Baiba Lāce, & Nicolas Chrestian. (2020). Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report. BMC Neurology. 20(1). 58–58. 6 indexed citations

Puisac, Beatriz, Íñigo Marcos‐Alcalde, Bernd Schwahn, et al.. (2018). Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New Patients. International Journal of Molecular Sciences. 19(4). 1010–1010. 23 indexed citations

Krūmiņa, Astrīda, Liāna Pliss, Gunita Zariņa, et al.. (2018). Population Genetics of Latvians in the Context of Admixture between North-Eastern European Ethnic Groups. Proceedings of the Latvian Academy of Sciences Section B Natural Exact and Applied Sciences. 72(3). 131–151. 3 indexed citations

10.

Gailīte, Linda, et al.. (2016). Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population. Archives of Medical Science. 3(3). 479–485. 19 indexed citations

11.

Pečulis, Raitis, et al.. (2016). Genetic linkage studies of a North Carolina macular dystrophy family. Medicina. 52(3). 180–186. 6 indexed citations

12.

Lāce, Baiba, et al.. (2014). IRF6 AP-2a binding site promoter polymorphism is associated with oral clefts in Latvia.. PubMed. 16(4). 132–6. 11 indexed citations

13.

Rots, Dmitrijs, et al.. (2014). Lack of Association between Polymorphisms in Genes MTHFR and MDR1 with Risk of Childhood Acute Lymphoblastic Leukemia. Asian Pacific Journal of Cancer Prevention. 15(22). 9707–9711. 18 indexed citations

14.

Lāce, Baiba, et al.. (2013). Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy. SHILAP Revista de lepidopterología. 2013. 1–3. 1 indexed citations

15.

Letra, Ariadne, Walid D. Fakhouri, Renato Menezes, et al.. (2012). Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate. PLoS ONE. 7(9). e45441–e45441. 43 indexed citations

16.

Vieira, Alexandre R., et al.. (2012). Risk of cancer in relatives of children born with isolated cleft lip and palate. American Journal of Medical Genetics Part A. 158A(6). 1503–1504. 35 indexed citations

17.

Lāce, Baiba, Linda Gailīte, Jānis Kloviņš, et al.. (2011). Association studies of candidate genes and cleft lip and palate taking into consideration geographical origin. European Journal Of Oral Sciences. 119(6). 413–417. 7 indexed citations

18.

Nikopensius, Tiit, Triin Jagomägi, Kaarel Krjutškov, et al.. (2010). Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate. Birth Defects Research Part A Clinical and Molecular Teratology. 88(9). 748–756. 37 indexed citations

19.

Vieira, Alexandre R., et al.. (2010). Mitochondrial DNA origins of the Latvian clefting population. Mitochondrion. 11(2). 357–359. 3 indexed citations

20.

Lāce, Baiba, et al.. (2008). Age of SERPINA1 Gene PI Z Mutation: Swedish and Latvian Population Analysis. Annals of Human Genetics. 72(3). 300–304. 18 indexed citations

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