Guillaume Smits

10.8k citations

55 papers · 4.7k indexed · 2 hit papers · h-index 24

Molecular Biology top 2%
Genetics top 1%
Reproductive Medicine top 1%
Cancer Research top 2%
Ecology, Evolution, Behavior and Systematics top 2%

Co-authors: Patrick Mardulyn Nicolas Dierckxsens Gilbert Vassart Sabine Costagliola Wolf Reik Andrew Keniry Michael Kyba Paul Monnier
Topics: Genomics and Rare Diseases (10 papers)Ovarian function and disorders (9 papers)Hypothalamic control of reproductive hormones (8 papers)
Cited by: Reproductive Medicine Molecular Biology Cancer Research
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences Nucleic Acids Research
Partner nations: Belgium United States United Kingdom

In The Last Decade

Guillaume Smits

53 papers receiving 4.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

NOVOPlasty: de novo assembly of organelle genomes from whole genome data

2016 2.0k citations Guillaume Smits et al. Nucleic Acids Research profile →
The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r

2012 657 citations Andrew Keniry, David Oxley et al. Nature Cell Biology profile →

Peers

Countries citing papers authored by Guillaume Smits

Since Specialization

Citations

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

Fields of papers citing papers by Guillaume Smits

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guillaume Smits

This figure shows the co-authorship network connecting the top 25 collaborators of Guillaume Smits. A scholar is included among the top collaborators of Guillaume Smits 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 Guillaume Smits. Guillaume Smits 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

#	Work	Indexed citations
1	A milder form of NSRP1‐associated neurodevelopmental disorder, caused by a missense variant in the nuclear localization signal 2024 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),Julie Soblet,Sonia Van Dooren,Catharina Olsen,Toon Janssen,(unknown),Chang‐Duk Jun,Guillaume Smits,Sandra Coppens,Catheline Vilain	0
2	Prioritization of oligogenic variant combinations in whole exomes 2024 ·Bioinformatics ·(unknown),Alexandre Renaux,Sofia Papadimitriou,Guillaume Smits,Ann Nowé,Tom Lenaerts	2
3	Comprehensive evaluation of the implementation of episignatures for diagnosis of neurodevelopmental disorders (NDDs) 2023 ·Human Genetics ·(unknown),(unknown),(unknown),(unknown),Bruno Pichon,(unknown),Catheline Vilain,Catharina Olsen,Sonia Van Dooren,Guillaume Smits,Matthieu Defrance	3
4	Pediatric pulmonary arterial hypertension due to a novel homozygous GDF2 missense variant affecting BMP9 processing and activity 2023 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Mírian Romitti,Laurence Dewachter,Jean‐Luc Vachiéry,Sabine Bailly,Sabine Costagliola,Guillaume Smits,Emmanuelle Tillet,Antoine Bondue	3
5	Salt-losing tubulopathy worsening the prognosis of renal sarcoidosis 2023 ·Journal of Nephrology ·(unknown),Alaín Le Moine,(unknown),(unknown),Lidia Ghisdal,(unknown),Guillaume Smits,Joëlle Nortier	0
6	Two siblings with Bosch-Boonstra-Schaaf optic atrophy syndrome due to parental gonadal mosaicism 2023 ·European Journal of Medical Genetics ·(unknown),Catheline Vilain,Koenraad Devriendt,Ingele Casteels,Guillaume Smits,Julie Soblet,Irina Balikova	1
7	Early‐onset and severe pulmonary arterial hypertension due to a novel compound heterozygous association of rare VHL mutations: A case report and review of existing data 2022 ·Pulmonary Circulation ·(unknown),Isabelle Migeotte,Céline Dewachter,Jean‐Luc Vachiéry,Guillaume Smits,Antoine Bondue	5
8	Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases 2022 ·Human Genetics and Genomics Advances ·Sofia Papadimitriou,(unknown),(unknown),Elfride De Baere,Bart Loeys,Miikka Vikkula,Guillaume Smits,Tom Lenaerts	11
9	Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants 2021 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),G. Garofalo,Marie Cassart,(unknown),Isabelle Vandernoot,Guillaume Smits,(unknown)	1
10	ORVAL: a novel platform for the prediction and exploration of disease-causing oligogenic variant combinations 2019 ·Nucleic Acids Research ·Alexandre Renaux,Sofia Papadimitriou,(unknown),(unknown),(unknown),Ann Nowé,Guillaume Smits,Tom Lenaerts	39
11	The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1rbreakdown → 2012 ·Nature Cell Biology ·Andrew Keniry,David Oxley,Paul Monnier,Michael Kyba,Luisa Dandolo,Guillaume Smits,Wolf Reik	657
12	High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta 2010 ·BMC Genetics ·Caroline Daelemans,Matthew E. Ritchie,Guillaume Smits,Sayeda Abu‐Amero,Ian Sudbery,Matthew S. Forrest,Susana Campino,Taane G. Clark,Philip Stanier,Dominic Kwiatkowski,Panos Deloukas,Emmanouil T. Dermitzakis,Simon Tavaré,Gudrun E. Moore,Ian Dunham	48
13	The specificity of binding of glycoprotein hormones to their receptors 2008 ·Cellular and Molecular Life Sciences ·Gianluigi Caltabiano,Mercedes Campillo,Anne De Leener,Guillaume Smits,Gilbert Vassart,Sabine Costagliola,Leonardo Pardo	44
14	Non‐coding transcripts in the H19 imprinting control region mediate gene silencing in transgenic Drosophila 2007 ·EMBO Reports ·Stefan Schoenfelder,Guillaume Smits,Peter Fraser,Wolf Reik,Renato Paro	37
15	Genetic predictors of ovarian hyperstimulation syndrome in women undergoing in vitro fertilization 2006 ·Nature Clinical Practice Endocrinology &#38 Metabolism ·Anne Delbaere,Guillaume Smits,Gilbert Vassart,Sabine Costagliola	8
16	Glycoprotein hormone receptors: link between receptor homodimerization and negative cooperativity 2005 ·The EMBO Journal ·Eneko Urizar,Lucia Montanelli,(unknown),Marco Bonomi,Stéphane Swillens,Céline Galès,Michel Bouvier,Guillaume Smits,Gilbert Vassart,Sabine Costagliola	227
17	Prediction of Severity of Symptoms in Iatrogenic Ovarian Hyperstimulation Syndrome by Follicle-Stimulating Hormone Receptor Ser⁶⁸⁰Asn Polymorphism 2004 ·The Journal of Clinical Endocrinology & Metabolism ·Caroline Daelemans,Guillaume Smits,Viviane De Maertelaer,Sabine Costagliola,Yvon Englert,Gilbert Vassart,Anne Delbaere	98
18	Lysine 183 and Glutamic Acid 157 of the TSH Receptor: Two Interacting Residues with a Key Role in Determining Specificity toward TSH and Human CG 2002 ·Molecular Endocrinology ·Guillaume Smits	16
19	Lysine 183 and Glutamic Acid 157 of the TSH Receptor: Two Interacting Residues with a Key Role in Determining Specificity toward TSH and Human CG 2002 ·Molecular Endocrinology ·Guillaume Smits,Cédric Govaerts,(unknown),Leonardo Pardo,Gilbert Vassart,Sabine Costagliola	49
20	An examination of different Percoll density gradients and magnetic activated cell sorting (MACS) for the enrichment of fetal erythroblasts from maternal blood 2000 ·Archives of Gynecology and Obstetrics ·Guillaume Smits,Wolfgang Holzgreve,S Hahn	21

About Guillaume Smits

Guillaume Smits is a scholar working on Reproductive Medicine, Genetics and Molecular Biology, having authored 55 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Ovarian function and disorders (9 papers) and Hypothalamic control of reproductive hormones (8 papers). The work is most often cited by research in Reproductive Medicine (748 citations), Molecular Biology (3.1k citations) and Cancer Research (668 citations). Guillaume Smits has collaborated with scholars based in Belgium, United States and United Kingdom. Frequent co-authors include Patrick Mardulyn, Nicolas Dierckxsens, Gilbert Vassart, Sabine Costagliola, Wolf Reik, Andrew Keniry, Michael Kyba, Paul Monnier, David Oxley and Luisa Dandolo. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

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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