Isabelle Vandernoot

9.4k total citations
16 papers, 102 citations indexed

About

Isabelle Vandernoot is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Isabelle Vandernoot has authored 16 papers receiving a total of 102 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Isabelle Vandernoot's work include Congenital heart defects research (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and interferon and immune responses (2 papers). Isabelle Vandernoot is often cited by papers focused on Congenital heart defects research (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and interferon and immune responses (2 papers). Isabelle Vandernoot collaborates with scholars based in Belgium, United States and Germany. Isabelle Vandernoot's co-authors include Achim Trubiroha, Robert Opitz, Sabine Costagliola, Johnny Deladoëy, Rasha Abu‐Khudir, Gauthier Remiche, Marc‐Phillip Hitz, Massimo Pandolfo, Grégor Andelfinger and Myriam Rai and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Development.

In The Last Decade

Isabelle Vandernoot

14 papers receiving 102 citations

Peers

Isabelle Vandernoot

GENET

EDM

PPCH

SURGE

Amy Shealy United States

Christel Thauvin-Robinet France

Maria Karaleftheri Greece

Abdulrahman Swaid Saudi Arabia

Salima El Chehadeh-Djebbar France

Vaitsa Tziaferi United Kingdom

Lilia Kraoua Tunisia

Judit Bigas Spain

Amy Shealy United States

Isabelle Vandernoot

87 ×1.4

75 ×1.8

GENET

16 ×0.6

EDM

12 ×1.1

PPCH

24 ×2.4

SURGE

Citations per year, relative to Isabelle Vandernoot Isabelle Vandernoot (= 1×) peers Amy Shealy

Countries citing papers authored by Isabelle Vandernoot

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Vandernoot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Vandernoot

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

All Works

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16 of 16 papers shown

Kadhim, Hazim, et al.. (2024). Early-Onset Autosomal Dominant Myopathy with Vacuolated Fibers and Tubular Aggregates but No Periodic Paralysis, in a Patient with the c.1583G>A (p.R528H) mutation in the CACNA1S Gene. Journal of Neuromuscular Diseases. 11(4). 871–875.

Smits, Guillaume, et al.. (2024). POT1 tumour predisposition: a broader spectrum of associated malignancies and proposal for additional screening program. European Journal of Human Genetics. 32(8). 980–986. 2 indexed citations

Segers, Kurt, Florence Benoit, Joachim Schulz, et al.. (2024). G2019S Mutation of Leucine-Rich Repeat Kinase 2 Is a Cause of Lewy Body Dementia in Patients With North African Ancestors. Alzheimer Disease & Associated Disorders. 38(4). 328–331. 1 indexed citations

Opitz, Robert, et al.. (2023). Mesodermal FGF and BMP govern the sequential stages of zebrafish thyroid specification. Development. 150(10). 3 indexed citations

Smits, Guillaume, et al.. (2022). Genetic testing in autoinflammatory diseases – past, current and future perspectives. European Journal of Internal Medicine. 106. 71–79. 5 indexed citations

Garofalo, G., et al.. (2021). Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants. SHILAP Revista de lepidopterología. 9(8). e04624–e04624. 1 indexed citations

Remiche, Gauthier, et al.. (2021). SPG43 and ALS-like syndrome in the same family due to compound heterozygous mutations of the C19orf12 gene: a case description and brief review. Neurogenetics. 22(1). 95–101. 1 indexed citations

Vandernoot, Isabelle, et al.. (2020). Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation. Clinical Genetics. 98(4). 416–417. 1 indexed citations

Vandernoot, Isabelle, et al.. (2020). Enhanced Canonical Wnt Signaling During Early Zebrafish Development Perturbs the Interaction of Cardiac Mesoderm and Pharyngeal Endoderm and Causes Thyroid Specification Defects. Thyroid. 31(3). 420–438. 11 indexed citations

10.

Jissendi, P., et al.. (2020). A New <b><i>DARS2</i></b> Mutation Discovered in an Adult Patient. SHILAP Revista de lepidopterología. 12(1). 107–113. 6 indexed citations

11.

Vandernoot, Isabelle, et al.. (2020). Case Report of an Unusual Tumor in an Adult With a TP53 Germline Mutation. Clinical Lymphoma Myeloma & Leukemia. 21(8). e645–e648.

12.

Pandolfo, Massimo, et al.. (2020). Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation. Neurology Genetics. 6(3). e420–e420. 14 indexed citations

13.

Wilkin, Françoise, Isabelle Vandernoot, Guillaume Smits, et al.. (2020). Prevalence and clinical impact of BRCA1/2 mutations in patients with de novo metastatic hormone-sensitive prostate cancer (mHSPC).. Journal of Clinical Oncology. 38(6_suppl). 44–44. 2 indexed citations

14.

Opitz, Robert, et al.. (2019). Small-Molecule Screening in Zebrafish Embryos Identifies Signaling Pathways Regulating Early Thyroid Development. Thyroid. 29(11). 1683–1703. 16 indexed citations

15.

Opitz, Robert, Marc‐Phillip Hitz, Isabelle Vandernoot, et al.. (2014). Functional Zebrafish Studies Based on Human Genotyping Point to Netrin-1 as a Link Between Aberrant Cardiovascular Development and Thyroid Dysgenesis. Endocrinology. 156(1). 377–388. 28 indexed citations

16.

Vandernoot, Isabelle, Hervé Sartelet, Rasha Abu‐Khudir, Jean‐Pierre Chanoine, & Johnny Deladoëy. (2012). Evidence for Calcitonin-Producing Cells in Human Lingual Thyroids. The Journal of Clinical Endocrinology & Metabolism. 97(3). 951–956. 11 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.

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