S. Heuertz

2.0k citations

40 papers · 883 indexed · h-index 18

Co-authors: M. C. Hors‐Cayla Martine Le Merrer J Frézal A. Sefiani Jacky Bonaventure Damian Labuda Jelena Martinović Valérie Cormier‐Daire
Topics: Connective tissue disorders research (11 papers)Genetic and rare skin diseases. (6 papers)Genomic variations and chromosomal abnormalities (4 papers)
Cited by: Genetics Molecular Biology Immunology and Allergy
Journals: Journal of Virology FEBS Letters The American Journal of Human Genetics
Partner nations: France Canada Germany

In The Last Decade

S. Heuertz

40 papers receiving 842 citations

Peers

Countries citing papers authored by S. Heuertz

Since Specialization

Citations

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

Fields of papers citing papers by S. Heuertz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Heuertz

This figure shows the co-authorship network connecting the top 25 collaborators of S. Heuertz. A scholar is included among the top collaborators of S. Heuertz 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 S. Heuertz. S. Heuertz 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	Thanatophoric dysplasia caused by double missense FGFR3 mutations 2009 ·American Journal of Medical Genetics Part A ·Stéphanie Pannier,Jelena Martinović,S. Heuertz,Anne‐Lise Delezoide,Arnold Münnich,Laurent Schibler,Valérie Serre,Laurence Legeai‐Mallet	16
2	Novel mutation and atlantoaxial dislocation in two siblings from India with Dyggve–Melchior–Clausen syndrome 2007 ·European Journal of Medical Genetics ·Katta M. Girisha,Valérie Cormier‐Daire,S. Heuertz,Rajendra V. Phadke,Shubha R. Phadke	8
3	Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia 2006 ·European Journal of Human Genetics ·S. Heuertz,Martine Le Merrer,Bernhard Zabel,Michael Wright,Laurence Legeai‐Mallet,Valérie Cormier‐Daire,Linda Gibbs,Jacky Bonaventure	65
4	X-linked spondyloepiphyseal dysplasia tarda: Novel and recurrent mutations in 13 European families 2004 ·Human Mutation ·Jörg Fiedler,Martine Le Merrer,Geert Mortier,S. Heuertz,Laurence Faivre,Rolf E. Brenner	19
5	Fluorescence Genotyping for Screening Cryptic Telomeric Rearrangements 2003 ·Molecular Cytogenetics ·Laurence Colleaux,S. Heuertz,Florence Molinari,Marlène Rio	5
6	Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation 2002 ·Journal of Medical Genetics ·Marlène Rio,Florence Molinari,S. Heuertz,Catherine Ozilou,Philippe Gosset,O Raoul,Valérie Cormier‐Daire,Aliza Amiel,Stanislas Lyonnet,(unknown),C Turleau,Marie‐Christine de Blois,M Prieur,Serge Romana,Michel Vekemans,Arnold Münnich,Laurence Colleaux	54
7	A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation 2001 ·European Journal of Human Genetics ·Laurence Colleaux,Marlène Rio,S. Heuertz,(unknown),C Turleau,Catherine Ozilou,Philippe Gosset,(unknown),Stanislas Lyonnet,Valérie Cormier‐Daire,Jeanne Amiel,Martine Le Merrer,(unknown),Marie‐Christine de Blois,Marguerite Prieur,Serge Romana,F. Cornélis,Michel Vekemans,Arnold Münnich	47
8	The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda 2001 ·The American Journal of Human Genetics ·Ági K. Gedeon,George E. Tiller,M. Le Merrer,S. Heuertz,Lisbeth Tranebjærg,David Chitayat,Stephen P. Robertson,Ian A. Glass,Ravi Savarirayan,William G. Cole,David L. Rimoin,Boris G. Kousseff,Hirofumi Ohashi,Bernhard Zabel,Arnold Münnich,Jozef Gécz,John C. Mulley	70
9	Filamin (FLN1),plexin (SEX), major palmitoylated proteinp55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 2000 ·American Journal of Medical Genetics ·Swaroop Aradhya,(unknown),Richard A. Lewis,David L. Nelson,Teresa Esposito,Alfredo Ciccodicola,Tiziana Bardaro,Michele D’Urso,Hayley Woffendin,Susan Kenwrick,Asma Smahi,S. Heuertz,Arnold Munnich,Nina S. Heiss,Annemarie Poustka,Athar H. Chishti	3
10	Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL) 1995 ·Human Genetics ·S. Heuertz,Asma Smahi,Andrew O.M. Wilkie,M. Le Merrer,P Maroteaux,M. C. Hors‐Cayla	17
11	Fine deletion mapping of the p22 region of the human X chromosome using a radiation-induced hybrid panel 1995 ·Cytogenetic and Genome Research ·S. Heuertz,Asma Smahi,Marek Sanak,(unknown),M. C. Hors‐Cayla	1
12	Refinement of the localization of the gene responsible for spondylo epiphyseal dysplasia in Xp22 1994 ·The American Journal of Human Genetics ·M. C. Hors‐Cayla,S. Heuertz,Asma Smahi	1
13	The Gene for Spondyloepiphyseal Dysplasia (SEDL) Maps to Xp22 between DXS16 and DXS92 1993 ·Genomics ·S. Heuertz,Marcel Nelen,Andrew O.M. Wilkie,Martine Le Merrer,(unknown),(unknown),Lisbeth Tranebjærg,David Bick,Ben C.J. Hamel,Bernard A. van Oost,P Maroteaux,M. C. Hors‐Cayla	20
14	Alport syndrome: a genetic study of 31 families 1992 ·Human Genetics ·(unknown),Marek Sanak,Georges Deschênes,Jing Zhou,Catherine Bonaïti‐Pellié,(unknown),S. Heuertz,Marie-Claire Gübler,M. Broyer,Jean‐Pierre Grünfeld,Karl Tryggvason,M. C. Hors‐Cayla	12
15	Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers 1991 ·Human Genetics ·A. Sefiani,Ridha Mrad,Louise R. Simard,Anne Vincent,Cécile Julier,(unknown),S. Heuertz,Niklas Dahl,J.‐F. Stalder,(unknown),Claude Moraine,(unknown),Julie L. Boyer,(unknown),Damian Labuda,M. C. Hors‐Cayla	32
16	[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]. 1990 ·PubMed ·(unknown),Jeffrey Kaplan,Anna Pelet,M Guilloud-Bataille,S. Heuertz,A Nivelon‐Chevallier,M Mathieu,(unknown),Hubert Journel,(unknown)	2
17	The gene for incontinentia pigmenti is assigned to Xq28 1989 ·Genomics ·A. Sefiani,Laurent Abel,S. Heuertz,Daniel Sinnett,(unknown),Damian Labuda,M. C. Hors‐Cayla	85
18	Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11 1988 ·Human Genetics ·A. Sefiani,Daniel Sinnett,Laurent Abel,(unknown),S. Heuertz,Ian Craig,Niall J. Fraser,Thomas Kruse,Moshe Frydman,(unknown),Schmutz Jl,S Gilgenkrantz,Grant A. Mitchell,J Frézal,S. Melançon,(unknown),Damian Labuda,M. C. Hors‐Cayla	25
19	Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome 1988 ·Human Genetics ·(unknown),A. Sefiani,M Guilloud-Bataille,S. Heuertz,B. Le Marec,J Frézal,P Maroteaux,M. C. Hors‐Cayla	29
20	Elvolution caryotypique de cellules hybrides homme x homme. 1972 ·Annales de Génétique ·M. C. Hors‐Cayla,(unknown),S. Heuertz	1

About S. Heuertz

S. Heuertz is a scholar working on Genetics, Pharmacy and Immunology and Allergy, having authored 40 papers that have together received 883 indexed citations. Recurring topics across this work include Connective tissue disorders research (11 papers), Genetic and rare skin diseases. (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (676 citations), Molecular Biology (494 citations) and Immunology and Allergy (43 citations). S. Heuertz has collaborated with scholars based in France, Canada and Germany. Frequent co-authors include M. C. Hors‐Cayla, Martine Le Merrer, J Frézal, A. Sefiani, Jacky Bonaventure, Damian Labuda, Jelena Martinović, Valérie Cormier‐Daire, Laurent Abel and Daniel Sinnett. Their work appears in journals such as Journal of Virology, FEBS Letters and The American Journal of Human Genetics.

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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