What is he best known for?
The fields of study he is best known for:
- Internal medicine
- Genetics
- DNA
The scientist’s investigation covers issues in Andrology, Oocyte, Cell biology, Human fertilization and Spindle apparatus.
David L. Keefe has included themes like Embryo and Blastocyst in his Andrology study.
His Cell biology research integrates issues from Enucleation, Oxidative stress and Apoptosis.
His studies deal with areas such as Telomere, Arsenic toxicity, Chromosome instability and Knockout mouse as well as Oxidative stress.
His study explores the link between Human fertilization and topics such as Intracytoplasmic sperm injection that cross with problems in Microtubule and Confocal.
His Spindle apparatus study combines topics in areas such as Staining, Anatomy and Cytoplast.
His most cited work include:
- Mitochondrial deoxyribonucleic acid deletions in oocytes and reproductive aging in women (240 citations)
- Quantification of hormone pulsatility via an approximate entropy algorithm (237 citations)
- Oxidative Phosphorylation-Dependent and -Independent Oxygen Consumption by Individual Preimplantation Mouse Embryos (205 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Cell biology, Andrology, Embryo, Internal medicine and Oocyte.
His research in Cell biology intersects with topics in Telomere, Molecular biology, Programmed cell death and Metaphase.
As part of the same scientific family, David L. Keefe usually focuses on Programmed cell death, concentrating on Mitochondrion and intersecting with Oxidative phosphorylation.
His study in Andrology is interdisciplinary in nature, drawing from both In vitro fertilisation, Pregnancy, Infertility, Blastocyst and Obstetrics.
His Embryo study deals with the bigger picture of Genetics.
His study focuses on the intersection of Oocyte and fields such as Human fertilization with connections in the field of Intracytoplasmic sperm injection.
He most often published in these fields:
- Cell biology (54.14%)
- Andrology (42.11%)
- Embryo (40.60%)
What were the highlights of his more recent work (between 2003-2016)?
- Andrology (42.11%)
- Embryo (40.60%)
- Cell biology (54.14%)
In recent papers he was focusing on the following fields of study:
Andrology, Embryo, Cell biology, Genetics and Endocrinology are his primary areas of study.
His biological study spans a wide range of topics, including In vitro fertilisation, Pregnancy, Ivf icsi and Blastocyst.
In the field of Embryo, his study on Intracytoplasmic sperm injection and Embryo morphology overlaps with subjects such as Genomic imprinting and Poor prognosis.
Cell biology connects with themes related to Telomere in his study.
His Endocrinology study combines topics from a wide range of disciplines, such as Oocyte, Oocyte activation, Internal medicine and Nocodazole.
His research in Oocyte focuses on subjects like Human fertilization, which are connected to Pellucida.
Between 2003 and 2016, his most popular works were:
- Müllerian inhibiting substance levels at the time of HCG administration in IVF cycles predict both ovarian reserve and embryo morphology (158 citations)
- Telomerase Deficiency Impairs Differentiation of Mesenchymal Stem Cells (106 citations)
- Telomerase Deficiency Impairs Differentiation of Mesenchymal Stem Cells (106 citations)
In his most recent research, the most cited papers focused on:
- Internal medicine
- Genetics
- DNA
His primary areas of study are Embryo, Cell biology, Genetics, Programmed cell death and Telomere.
His studies in Embryo integrate themes in fields like Gestation and Pregnancy rate.
His Cell biology study incorporates themes from Stem cell transplantation for articular cartilage repair, Adult stem cell and Molecular biology.
His Genetics study typically links adjacent topics like Andrology.
The various areas that he examines in his Programmed cell death study include Toxicity and Blastocyst.
His research investigates the link between Intracytoplasmic sperm injection and topics such as Anatomy that cross with problems in Oocyte.
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