Marie-Laure Kottler

1.7k total citations
23 papers, 981 citations indexed

About

Marie-Laure Kottler is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Marie-Laure Kottler has authored 23 papers receiving a total of 981 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Marie-Laure Kottler's work include Genetic Syndromes and Imprinting (6 papers), Vitamin D Research Studies (6 papers) and Genomics and Rare Diseases (5 papers). Marie-Laure Kottler is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Vitamin D Research Studies (6 papers) and Genomics and Rare Diseases (5 papers). Marie-Laure Kottler collaborates with scholars based in France, United States and Canada. Marie-Laure Kottler's co-authors include Arnaud Murat, Philippe Bouchard, Raymond Counis, Glenville Jones, Jacques Young, Sławomir Wołczyński, Karl P. Schlingmann, Catherine Dodé, Marc Delpech and Jacqueline Levilliers and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Bone and Mineral Research and PLoS Genetics.

In The Last Decade

Marie-Laure Kottler

22 papers receiving 958 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Marie-Laure Kottler France 15 456 406 361 253 153 23 981
Albert de la Chapelle Finland 13 544 1.2× 477 1.2× 407 1.1× 133 0.5× 56 0.4× 15 1.3k
Michèle Mathieu France 9 341 0.7× 310 0.8× 247 0.7× 60 0.2× 37 0.2× 18 622
Junji Iwasaki Japan 15 223 0.5× 97 0.2× 125 0.3× 219 0.9× 126 0.8× 39 904
Kirsi Vaaralahti Finland 16 332 0.7× 283 0.7× 438 1.2× 198 0.8× 14 0.1× 35 719
Hélène Buteau France 9 384 0.8× 246 0.6× 137 0.4× 370 1.5× 16 0.1× 9 914
Anne Guiochon‐Mantel France 18 473 1.0× 356 0.9× 665 1.8× 374 1.5× 21 0.1× 24 1.3k
Vassos Neocleous Cyprus 15 444 1.0× 261 0.6× 73 0.2× 223 0.9× 34 0.2× 61 728
Frédéric Brioude France 21 772 1.7× 796 2.0× 181 0.5× 138 0.5× 69 0.5× 49 1.2k
F. R. Boockfor United States 15 321 0.7× 230 0.6× 302 0.8× 617 2.4× 11 0.1× 26 1.1k
Susan J. Allen United States 15 439 1.0× 367 0.9× 71 0.2× 28 0.1× 70 0.5× 25 752

Countries citing papers authored by Marie-Laure Kottler

Since Specialization
Citations

This map shows the geographic impact of Marie-Laure Kottler'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 Kottler 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 Kottler more than expected).

Fields of papers citing papers by Marie-Laure Kottler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie-Laure Kottler

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

All Works

20 of 20 papers shown
1.
2.
Kaufmann, Martin, Karl P. Schlingmann, Arnaud Molin, et al.. (2020). Differential diagnosis of vitamin D–related hypercalcemia using serum vitamin D metabolite profiling. Journal of Bone and Mineral Research. 36(7). 1340–1350. 29 indexed citations
3.
Hanna, Patrick, Virginie Grybek, Guiomar Pérez de Nanclares, et al.. (2018). Genetic and Epigenetic Defects at the GNAS Locus Lead to Distinct Patterns of Skeletal Growth but Similar Early-Onset Obesity. Journal of Bone and Mineral Research. 33(8). 1480–1488. 36 indexed citations
4.
Jones, Glenville, Marie-Laure Kottler, & Karl P. Schlingmann. (2017). Genetic Diseases of Vitamin D Metabolizing Enzymes. Endocrinology and Metabolism Clinics of North America. 46(4). 1095–1117. 43 indexed citations
5.
Castiglioni, Claudia, et al.. (2017). Pseudohypoparathyroidism type 1B associated with assisted reproductive technology. Journal of Pediatric Endocrinology and Metabolism. 30(10). 1125–1132. 9 indexed citations
6.
Molin, Arnaud, et al.. (2017). Calcium pyrophosphate deposition disease revealing a hypersensitivity to vitamin D. Joint Bone Spine. 84(3). 349–351. 4 indexed citations
7.
Molin, Arnaud, François Feillet, Arnaud Wiedemann, et al.. (2016). Two French Families with Vitamin D Dependency Rickets Type 1B Harbor Homozygous Recessive Expression Of CYP2R1 Mutations L99P and G42_L46DEL INSR. 86. 1 indexed citations
8.
Auger, Julie, Amandine Baptiste, Imane Benabbad, et al.. (2016). Genotype-Phenotype Relationship in Patients and Relatives with <b><i>SHOX</i></b> Region Anomalies in the French Population. Hormone Research in Paediatrics. 86(5). 309–318. 4 indexed citations
9.
Tolédano, Daniel, et al.. (2015). Diagnosis and Management of Congenital Hypothyroidism Associated with Pseudohypoparathyroidism. Hormone Research in Paediatrics. 83(2). 111–117. 5 indexed citations
10.
Choi, Jin‐Ho, Ravikumar Balasubramanian, Phil H. Lee, et al.. (2015). Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency. The Journal of Clinical Endocrinology & Metabolism. 100(10). E1378–E1385. 18 indexed citations
11.
Zbucka-Krętowska, Monika, et al.. (2011). Expression of estrogen receptors in the pelvic floor of pre- and post-menopausal women presenting pelvic organ prolapse. Folia Histochemica et Cytobiologica. 49(3). 521–527. 16 indexed citations
12.
Kottler, Marie-Laure, Nicolas Richard, Olivier Chabre, Sophie Alain, & John K. Young. (2010). FSHbeta gene mutation in a female with delayed puberty and hypogonadism: response to recombinant human FSH.. Folia Histochemica et Cytobiologica. 47(5). S55–8. 6 indexed citations
13.
Kottler, Marie-Laure, Yen-Yin Chou, Olivier Chabre, et al.. (2009). A new FSHβ mutation in a 29-year-old woman with primary amenorrhea and isolated FSH deficiency: functional characterization and ovarian response to human recombinant FSH. European Journal of Endocrinology. 162(3). 633–641. 33 indexed citations
14.
Dodé, Catherine, Luís Teixeira, Jacqueline Levilliers, et al.. (2006). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. 2(10). e175–e175. 315 indexed citations
15.
Linglart, Agnès, et al.. (2002). GNAS1Lesions in Pseudohypoparathyroidism Ia and Ic: Genotype Phenotype Relationship and Evidence of the Maternal Transmission of the Hormonal Resistance. The Journal of Clinical Endocrinology & Metabolism. 87(1). 189–197. 93 indexed citations
16.
Nguyen, T. M., Marie-Laure Kottler, H. Guillozo, et al.. (2002). Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D. Journal of Bone and Mineral Research. 17(9). 1728–1737. 30 indexed citations
17.
Niccoli‐Sire, Patricia, Arnaud Murat, V. Rohmer, et al.. (2001). Familial Medullary Thyroid Carcinoma with Noncysteine RET Mutations: Phenotype-Genotype Relationship in a Large Series of Patients. The Journal of Clinical Endocrinology & Metabolism. 86(8). 3746–3753. 112 indexed citations
18.
Kottler, Marie-Laure, Stéphanie Chauvin, Najiba Lahlou, et al.. (2000). A New Compound Heterozygous Mutation of the Gonadotropin-Releasing Hormone Receptor (L314X, Q106R) in a Woman with Complete Hypogonadotropic Hypogonadism: Chronic Estrogen Administration Amplifies the Gonadotropin Defect1. The Journal of Clinical Endocrinology & Metabolism. 85(9). 3002–3008. 57 indexed citations
19.
Kottler, Marie-Laure, Raymond Counis, & Philippe Bouchard. (1999). Mutations of the GnRH Receptor Gene. Archives of Medical Research. 30(6). 481–485. 23 indexed citations
20.
Kottler, Marie-Laure, et al.. (1994). Gonadal and adrenal catheterization during adrenal suppression and gonadal stimulation in a patient with bilateral testicular tumors and congenital adrenal hyperplasia.. The Journal of Clinical Endocrinology & Metabolism. 79(5). 1390–1394. 43 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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