What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Genetics, Gene, Internal medicine, Germ cell and Premature ovarian failure.
His work is connected to Transcription factor, Mutation, Missense mutation, Exon and Genome-wide association study, as a part of Genetics.
His research integrates issues of Endocrinology and Gynecology in his study of Internal medicine.
Aleksandar Rajkovic has researched Germ cell in several fields, including Gene expression, Dosage compensation, Cell signaling and Somatic cell.
The various areas that he examines in his Premature ovarian failure study include Chromosome instability, X chromosome, Hypergonadotropic hypogonadism and Candidate gene.
In Folliculogenesis, Aleksandar Rajkovic works on issues like Homeobox, which are connected to Cell biology.
His most cited work include:
- Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer (463 citations)
- A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33 (456 citations)
- Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. (432 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Genetics, Gene, Internal medicine, Cell biology and Molecular biology.
Genetics and Premature ovarian failure are frequently intertwined in his study.
He combines subjects such as Endocrinology and Oncology with his study of Internal medicine.
His work in Cell biology tackles topics such as Germ cell which are related to areas like Somatic cell.
As a part of the same scientific study, Aleksandar Rajkovic usually deals with the Molecular biology, concentrating on Gene expression and frequently concerns with In silico.
His Pancreatic cancer research focuses on Odds ratio and how it connects with Prospective cohort study.
He most often published in these fields:
- Genetics (47.28%)
- Gene (18.48%)
- Internal medicine (18.48%)
What were the highlights of his more recent work (between 2015-2021)?
- Genetics (47.28%)
- Gene (18.48%)
- Exome sequencing (9.24%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Genetics, Gene, Exome sequencing, Bioinformatics and Pregnancy.
His works in Male infertility, X chromosome, Phenotype, Microarray analysis techniques and Medical genetics are all subjects of inquiry into Genetics.
The X chromosome study combines topics in areas such as Oocyte, Ovarian reserve and Premature ovarian failure.
His Gene study integrates concerns from other disciplines, such as Etiology and Hypergonadotropic hypogonadism.
His study in Bioinformatics is interdisciplinary in nature, drawing from both Endocrinology, Female infertility, Internal medicine, DNA repair and Comparative genomic hybridization.
His Internal medicine research is multidisciplinary, incorporating elements of Heterozygote advantage, Oncology and Leiomyoma.
Between 2015 and 2021, his most popular works were:
- Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update. (51 citations)
- MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency. (51 citations)
- Subpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate (44 citations)
In his most recent research, the most cited papers focused on:
His main research concerns Genetics, Exome sequencing, Bioinformatics, Male infertility and Sanger sequencing.
His research on Genetics often connects related topics like Gonad.
His Exome sequencing research includes elements of Heredity, Menopause, Genetic association and Gonadal dysgenesis.
His Bioinformatics research integrates issues from Pregnancy, Chromosome breakage, Endocrinology, DNA damage and DNA repair.
As part of the same scientific family, Aleksandar Rajkovic usually focuses on Pregnancy, concentrating on X chromosome and intersecting with Oocyte and Oogenesis.
His Male infertility study incorporates themes from Nonsense mutation, Missense mutation, Azoospermia and Candidate gene.
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