Lina Basel‐Vanagaite

8.1k total citations
111 papers, 3.6k citations indexed

About

Lina Basel‐Vanagaite is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lina Basel‐Vanagaite has authored 111 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 57 papers in Genetics and 27 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lina Basel‐Vanagaite's work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (20 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Lina Basel‐Vanagaite is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (20 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Lina Basel‐Vanagaite collaborates with scholars based in Israel, United States and Germany. Lina Basel‐Vanagaite's co-authors include Rachel Straussberg, Nurit Magal, Christopher A. Walsh, William B. Dobyns, Adria Bodell, Xianhua Piao, A. Micheil Innes, Metsada Pasmanik‐Chor, Bernard S. Chang and Mordechai Shohat and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Lina Basel‐Vanagaite

105 papers receiving 3.5k citations

Peers

Countries citing papers authored by Lina Basel‐Vanagaite

Since Specialization

Citations

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

Fields of papers citing papers by Lina Basel‐Vanagaite

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lina Basel‐Vanagaite. 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 Lina Basel‐Vanagaite. The network helps show where Lina Basel‐Vanagaite may publish in the future.

Co-authorship network of co-authors of Lina Basel‐Vanagaite

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

All Works

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	Is There an Alternative “Advanced Maternal Age” Threshold for Recommendation of Invasive Prenatal Testing?	Journal of Obstetrics and Gynaecology Canada	Idit Maya, Sarit Kahana et al.	0
2	Fetal whole genome sequencing as a clinical diagnostic tool: Advantages, limitations and pitfalls	Best Practice & Research Clinical Obstetrics & Gynaecology	Lina Basel‐Vanagaite et al.	2
3	Regions of Homozygocity size patterns among diverse ethnic groups in Israel: Toward tailored diagnostic reporting thresholds	American Journal of Medical Genetics Part A	Idit Maya, Michal Levy et al.	0
4	Exploring the human genomic landscape: patterns of common homozygosity regions in a large middle eastern cohort	Human Molecular Genetics	Lena Sagi‐Dain, Michal Levy et al.	0
5	Machine learning‐enhanced noninvasive prenatal testing of monogenic disorders	Prenatal Diagnosis	Noa Liscovitch‐Brauer, Tom Rabinowitz et al.	4
6	P766: A combined Bayesian inference and machine-learning approach for prenatal screening by cell free DNA of monogenic disorders	SHILAP Revista de lepidopterología	Noa Liscovitch‐Brauer, Tom Rabinowitz et al.	1
7	Patterns of mosaicism for sequence and copy-number variants discovered through clinical deep sequencing of disease-related genes in one million individuals	The American Journal of Human Genetics	Rebecca Truty, Susan Rojahn et al.	8
8	A nonsense variant in the second exon of the canonical transcript of NSD1 does not cause Sotos syndrome	American Journal of Medical Genetics Part A	Noa Ruhrman‐Shahar, Nurit Assia Batzir et al.	1
9	Chromosomal Microarray vs. NIPS: Analysis of 5541 Low-Risk Pregnancies	Obstetrical & Gynecological Survey	Lena Sagi‐Dain, Sarit Kahana et al.	1
10	Bayesian-based noninvasive prenatal diagnosis of single-gene disorders	Genome Research	Tom Rabinowitz, David E. Golan et al.	27
11	A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder	European Journal of Paediatric Neurology	Naama Orenstein, Hadassa Goldberg‐Stern et al.	23
12	Keppen-Lubinsky Syndrome Is Caused by Mutations in the Inwardly Rectifying K+ Channel Encoded by KCNJ6	The American Journal of Human Genetics	Andrea Masotti, Paolo Uva et al.	86
13	Transient Infantile Hypertriglyceridemia, Fatty Liver, and Hepatic Fibrosis Caused by Mutated GPD1, Encoding Glycerol-3-Phosphate Dehydrogenase 1	The American Journal of Human Genetics	Lina Basel‐Vanagaite, Noam Zevit et al.	73
14	X‐linked mental retardation with alacrima and achalasia—Triple A syndrome or a new syndrome?	American Journal of Medical Genetics Part A	Daphna Marom, Charles E. Schwartz et al.	4
15	Acute lymphoblastic leukemia in Weaver syndrome	American Journal of Medical Genetics Part A	Lina Basel‐Vanagaite	20
16	Familial hydrocephalus with normal cognition and distinctive radiological features	American Journal of Medical Genetics Part A	Lina Basel‐Vanagaite, Liora Kornreich et al.	3
17	A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly	The American Journal of Human Genetics	Ganeshwaran H. Mochida, Muhammad Mahajnah et al.	107
18	Genetic Carrier Screening for Spinal Muscular Atrophy and Spinal Muscular Atrophy with Respiratory Distress 1 in an Isolated Population in Israel	Genetic Testing	Lina Basel‐Vanagaite, Ellen Taub et al.	22
19	G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex	Science	Xianhua Piao, R. Sean Hill et al.	405
20	An Autosomal Recessive Form of Bilateral Frontoparietal Polymicrogyria Maps to Chromosome 16q12.2-21	The American Journal of Human Genetics	Xianhua Piao, Lina Basel‐Vanagaite et al.	84

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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