Marie‐Laure Sobrier

2.8k citations

50 papers · 2.0k indexed · h-index 24

Endocrinology, Diabetes and Metabolism top 0.5%
- Growth Hormone and Insulin-like Growth Factors 24
Genetics top 2%
- Genetic Syndromes and Imprinting 12
- Digestive system and related health 5
Cancer Research top 10%
- Cancer, Hypoxia, and Metabolism 4
Molecular Biology top 10%
- Epigenetics and DNA Methylation 5
- Congenital heart defects research 4
Cardiology and Cardiovascular Medicine top 10%
Cellular and Molecular Neuroscience
- Neurobiology and Insect Physiology Research 9
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 4

Co-authors: Serge Amselem Philippe Duquesnoy Michel Goossens Bénédicte Duriez Irène Netchine Florence Dastot Jacques Pantel B. Dastugue
Cited by: Endocrinology, Diabetes and Metabolism Genetics Cancer Research
Partner nations: France United States Belgium

In The Last Decade

Marie‐Laure Sobrier

48 papers receiving 2.0k citations

Peers

Countries citing papers authored by Marie‐Laure Sobrier

Since Specialization

Citations

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

Fields of papers citing papers by Marie‐Laure Sobrier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie‐Laure Sobrier. 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 Marie‐Laure Sobrier. The network helps show where Marie‐Laure Sobrier may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Marie‐Laure Sobrier, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Marie‐Laure Sobrier Line = papers co-authored together Marie‐Laure Sobrier links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	IGF2: Development, Genetic and Epigenetic Abnormalities Céline Sélénou,Frédéric Brioude,Éloïse Giabicani,Marie‐Laure Sobrier,Irène Netchine	2022	57
2	Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants Aurélie Pham,Marie‐Laure Sobrier,Éloïse Giabicani,Marilyne Le Jules Fernandes,Delphine Mitanchez,Frédéric Brioude,Irène Netchine	2021	3
3	Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders Walid Abi Habib,Frédéric Brioude,Salah Azzi,Sylvie Rossignol,Agnès Linglart,Marie‐Laure Sobrier,Éloïse Giabicani,Virginie Steunou,Madeleine D. Harbison,Yves Le Bouc,Irène Netchine	2019	33
4	Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern Marie Legendre,Florence Dastot,Nathalie Collot,Philippe Duquesnoy,Enzo Cohen,Marie‐Laure Sobrier,Paola Adiceam,Donald Anderson,S. Baron,Sylvie Cabrol,Bert Callewaert,Maryse Cartigny,Margarita Craen,Patricia Crock,Asmahane Ladjouze,Cecilia Lazea,Michel Polak,Lars Sävendahl,Asmae Touzani,Serge Amselem	2016	1
5	Screening of LHX2 in patients presenting growth retardation with posterior pituitary and ocular abnormalities C. Pérez,Florence Dastot‐Le Moal,Nathalie Collot,Marie Legendre,Isabelle Abadie,A Bertrand,Serge Amselem,Marie‐Laure Sobrier	2012	8
6	A novel POU1F1 mutation (p.Thr168IlefsX7) associated with an early and severe form of combined pituitary hormone deficiency: functional analysis and follow-up from infancy to adulthood Yardena Tenenbaum‐Rakover,Marie‐Laure Sobrier,Serge Amselem	2011	11
7	Unusual Phenotypic Features in a Patient with a Novel Splice Mutation in the GHRHR Gene Latifa Hilal,Yassir Hajaji,Marie-Pierre Vié-Luton,Zeina Ajaltouni,Bouchra Benazzouz,M. Chana,A. Chraïbi,Abdelkrim Kadiri,Serge Amselem,Marie‐Laure Sobrier	2008	23
8	Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development Marie‐Laure Sobrier,Tania Attié‐Bitach,Irène Netchine,Férechté Encha‐Razavi,Michel Vekemans,Serge Amselem	2004	43
9	Species-specific Alternative Splice Mimicry at the Growth Hormone Receptor Locus Revealed by the Lineage of Retroelements during Primate Evolution Jacques Pantel,Kalotina Machinis,Marie‐Laure Sobrier,Philippe Duquesnoy,Michel Goossens,Serge Amselem	2000	162
10	Evolutionary divergence of the truncated growth hormone receptor isoform in its ability to generate a soluble growth hormone binding protein Florence Dastot,Philippe Duquesnoy,Marie‐Laure Sobrier,Michel Goossens,Serge Amselem	1998	24
11	Nine Novel Growth Hormone Receptor Gene Mutations in Patients with Laron Syndrome¹ Marie‐Laure Sobrier,Florence Dastot,Philippe Duquesnoy,Nurgün Kandemir,N Yordam,Michel Goossens,Serge Amselem	1997	52
12	Pituitary Stalk Interruption Syndrome: A Clinical-Biological-Genetic Assessment of Its Pathogenesis¹ Graziella Pinto,Irène Netchine,Marie‐Laure Sobrier,Françis Brunelle,J.C. Souberbielle,Raja Brauner	1997	86
13	Expression and binding properties of two isoforms of the human growth hormone receptor Marie‐Laure Sobrier,Philippe Duquesnoy,Bénédicte Duriez,Serge Amselem,Michel Goossens	1993	95
14	Molecular Genetics of Laron-Type GH Insensitivity Syndrome Michel Goossens,Serge Amselem,Philippe Duquesnoy,Marie‐Laure Sobrier	1993	1
15	A naturally occurring growth hormone receptor mutation: in vivo and in vitro evidence for the functional importance of the WS motif common to all members of the cytokine receptor superfamily. Bénédicte Duriez,Marie‐Laure Sobrier,Philippe Duquesnoy,Michèle Tixier‐Boichard,Eddy Decuypere,Gérard Coquerelle,Michal Zeman,M. Goossens,Serge Amselem	1993	46
16	Recurrent nonsense mutations in the growth hormone receptor from patients with Laron dwarfism. Serge Amselem,Marie‐Laure Sobrier,Philippe Duquesnoy,R Rappaport,M C Postel-Vinay,M Gourmelen,Bruno Dallapiccola,Michel Goossens	1991	72
17	Regulatory elements in the first intron contribute to transcriptional regulation of the β₃tubulin gene by 20-hydroxyecdysone inDrosophilaKc cells Alain Bruhat,Sylvette Tourmente,S. Chapel,Marie‐Laure Sobrier,J.L. Couderc,B. Dastugue	1990	37
18	20-OH-ecdysone regulates 60 C β tubulin gene expression in Kc cells and during Drosophila development Marie‐Laure Sobrier,S. Chapel,J.L. Couderc,D. Micard,P. Lécher,Ghislaine Sommé‐Martin,B. Dastugue	1989	8
19	Molecular study of the retrovirus-like transposable element 412, a 20-OH ecdysone responsive repetitive sequence inDrosophilacultured cells D. Micard,J.L. Couderc,Marie‐Laure Sobrier,G Giraud,B. Dastugue	1988	15
20	Expression of a new β tubulin subunit is induced by 20-hydroxyecdysone in drosophila cultured cells Marie‐Laure Sobrier,J.L. Couderc,S. Chapel,B. Dastugue	1986	16

About Marie‐Laure Sobrier

Marie‐Laure Sobrier is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Cellular and Molecular Neuroscience, having authored 50 papers that have together received 2.0k indexed citations. Recurring topics across this work include Growth Hormone and Insulin-like Growth Factors (24 papers), Genetic Syndromes and Imprinting (12 papers), Neurobiology and Insect Physiology Research (9 papers), Digestive system and related health (5 papers), Epigenetics and DNA Methylation (5 papers), Congenital heart defects research (4 papers), Cancer, Hypoxia, and Metabolism (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.3k citations), Genetics (834 citations) and Cancer Research (213 citations). Marie‐Laure Sobrier has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Serge Amselem, Philippe Duquesnoy, Michel Goossens, Bénédicte Duriez, Irène Netchine, Florence Dastot, Jacques Pantel, B. Dastugue, Mohamad Maghnie and M Goossens.

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