Update cv-one-page.tex

Author: mfoll

cv-one-page.tex

@@ -290,21 +290,18 @@ \section{Personal Statement}
 developing new statistical and computational methods to analyze large genomic datasets, including
 approaches for Bayesian inference, population genetics, and variant detection. Over the past decade, I
 have led interdisciplinary teams integrating genomics, transcriptomics, and pathology imaging data to
-advance translational cancer research. In addition to my role as Team Leader, I also coordinate the
-bioinformatics efforts at the International Agency for Research on Cancer (IARC-WHO). I am particularly
-involved in the molecular characterization of thoracic tumors such as lung neuroendocrine
-neoplasms and malignant pleural mesothelioma; in 2015, I created the Rare Cancers Genomics initiative
+advance translational cancer research, with a particular focus on thoracic tumors. In addition to my role as Team Leader, I also coordinate the
+bioinformatics efforts at the International Agency for Research on Cancer (IARC-WHO). In 2015, I created the Rare Cancers Genomics initiative
 together with Dr. Lynnette Fernandez-Cuesta. As part of these efforts, I have developed and supervised
 multiple open-source software projects aimed at ultra-sensitive variant calling, integrative multi-omics
-pipelines, and, more recently, deep-learning–based image analysis, which have accelerated the discovery
-of new diagnostic and prognostic biomarkers.
+pipelines, and deep-learning–based image analysis.
 
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 \section{Publications}
 \ \\
-82 publications in international peer-reviewed scientific journals, including 9 publications as first/co-first author, and 15 publications as last/co-last/corresponding author.
+83 publications in international peer-reviewed scientific journals, including 9 publications as first/co-first author, and 16 publications as last/co-last/corresponding author.
 
-14'406 total citations, h-index: 44 (source: \href{https://scholar.google.com/citations?hl=en&user=vzZPQj8AAAAJ&view_op=list_works&sortby=pubdate}{Google Scholar}).
+14'683 total citations, h-index: 45 (source: \href{https://scholar.google.com/citations?hl=en&user=vzZPQj8AAAAJ&view_op=list_works&sortby=pubdate}{Google Scholar}), named a 2024 Top Scholar by \href{https://scholargps.com/scholars/36665698545984/matthieu-foll}{ScholarGPS} (top 0.5\% of all scholars worldwide) in \href{https://scholargps.com/top-scholars?year=2024&ranking_duration=LIFETIME&specialty=Genomics&p=82&e_ref=be75210910e03c3129a7#1631}{Genomics} and \href{https://scholargps.com/top-scholars?year=2024&ranking_duration=LIFETIME&specialty=Genotyping&p=12&e_ref=be75210910e03c3129a7#236}{Genotyping}.
 
 Full list available at \href{https://scholar.google.com/citations?hl=en&user=vzZPQj8AAAAJ&view_op=list_works&sortby=pubdate}{Google Scholar} and  \href{https://www.ncbi.nlm.nih.gov/myncbi/matthieu.foll.1/bibliography/public/}{My NCBI Bibliography}.