Jasmine Parma

6.7k citations
66 papers · 4.7k · 1 hit paper · h-index 35

Impact in

Papers in

  • Endocrinology, Diabetes and Metabolism 35
    • Thyroid Disorders and Treatments 24
    • Thyroid Cancer Diagnosis and Treatment 13
    • Growth Hormone and Insulin-like Growth Factors 4
  • Molecular Biology 19
    • Glycosylation and Glycoproteins Research 3
    • Congenital heart defects research 3
    • RNA and protein synthesis mechanisms 3
Co-authors
Gilbert Vassart (41 shared papers)Laurence Duprez (10 shared papers)Jacqueline Van Sande (11 shared papers)Jacques E. Dumont (9 shared papers)J. Van Sande (8 shared papers)Massimo Tonacchera (7 shared papers)Pascale Cochaux (8 shared papers)Christine Gervy (2 shared papers)
Journals
The Journal of Clinical Endocrinology & Metabolism (15 papers)European Journal of Endocrinology (4 papers)Journal of Clinical Investigation (2 papers)Molecular and Cellular Endocrinology (2 papers)The Journal of Pediatrics (2 papers)
Partner nations
BelgiumFranceUnited States

In The Last Decade

Jasmine Parma

65 papers receiving 4.5k citations

Jasmine Parma's Hit Papers

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas 1993 · 727 citations
7270+11+22Years since publication200400600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 1993 Nature

Peers

Jasmine Parma
Comparison fields: 5 of 100
  • Endocrinology, Diabetes and Metabolism 2.5k
  • Reproductive Medicine 339
  • Cellular and Molecular Neuroscience 701
  • Endocrine and Autonomic Systems 230
  • Molecular Biology 2.0k
Replace G I Bell with:
G I Bell United States
Lucia Vallar Italy
Anna Spada Italy
Laurence Duprez Belgium
Coimbatore B. Srikant Canada
Leonardo Guasti United Kingdom
Yoshiharu Murata Japan
Knut Krohn Germany
Gianfranco Fenzi Italy
Bethel Stannard United States
Jasmine Parma relative to G I Bell United States G I Bell's profile →
Citations per field
00.5×2×3×3.9×
G I Bell · 1×
Citations per year

Countries citing papers authored by Jasmine Parma

Since Specialization
Citations

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

Fields of papers citing papers by Jasmine Parma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jasmine Parma, 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 Jasmine Parma Line = papers co-authored together Jasmine Parma links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 66 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas
Nature ·Jasmine Parma, Laurence Duprez, Jacqueline Van Sande, Pascale Cochaux, Christine Gervy, Jean Mockel, Jacques E. Dumont, Gilbert Vassart
Hit paper breakdown →		1993727
2
Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism
Nature Genetics ·Laurence Duprez, Jasmine Parma, Jacqueline Van Sande, Anouk Allgeier, Jacques Leclère, Claire Schvartz, M J Delisle, M Decoulx, Jacques Orgiazzi, Jacques E. Dumont, Gilbert Vassart
1994296
3
Congenital Hyperthyroidism Caused by a Mutation in the Thyrotropin-Receptor Gene
New England Journal of Medicine ·Peter Kopp, Jacqueline Van Sande, Jasmine Parma, Laurence Duprez, H Gerber, E Joss, J. Larry Jameson, Jacques E. Dumont, Gilbert Vassart
1995227
4
Localization of adenylyl and guanylyl cyclase in rat brain by in situ hybridization: comparison with calmodulin mRNA distribution
Journal of Neuroscience ·Isao Matsuoka, Galicia Giuili, Madeleine Poyard, Dominique Stengel, Jasmine Parma, Georges Guellaën, Jacques Hanoune
1992215
5
Somatic and germline mutations of the TSH receptor gene in thyroid diseases.
The Journal of Clinical Endocrinology & Metabolism ·J. Van Sande, Jasmine Parma, Massimo Tonacchera, S. Swillens, J.E. Dumont, Gilbert Vassart
1995201
6
Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3',5'-monophosphate and inositol phosphate-Ca2+ cascades.
Molecular Endocrinology ·Jasmine Parma, J. Van Sande, S. Swillens, Massimo Tonacchera, J.E. Dumont, Gilbert Vassart
1995199
7
Familial Gestational Hyperthyroidism Caused by a Mutant Thyrotropin Receptor Hypersensitive to Human Chorionic Gonadotropin
New England Journal of Medicine ·Patrice Rodien, C Brémont, Marie-Laure Raffin Sanson, Jasmine Parma, Jacqueline Van Sande, Sabine Costagliola, Jean-Pierre Luton, Gilbert Vassart, Laurence Duprez
1998186
8
Diversity and Prevalence of Somatic Mutations in the Thyrotropin Receptor and Gsα Genes as a Cause of Toxic Thyroid Adenomas1
The Journal of Clinical Endocrinology & Metabolism ·Jasmine Parma, Laurence Duprez, Jacqueline Van Sande, J Hermans, P Rocmans, Guy Van Vliet, Sabine Costagliola, Patrice Rodien, Jacques E. Dumont, Gilbert Vassart
1997186
9
Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.
Journal of Clinical Investigation ·Marc Abramowicz, L Duprez, Jasmine Parma, G Vassart, Claudine Heinrichs
1997173
10
Autosomal Dominant Transmission of Congenital Thyroid Hypoplasia Due to Loss-of-Function Mutation of PAX81
The Journal of Clinical Endocrinology & Metabolism ·Catheline Vilain, Catherine Rydlewski, Laurence Duprez, Claudine Heinrichs, Marc Abramowicz, P Malvaux, B. Renneboog, Jasmine Parma, Sabine Costagliola, Gilbert Vassart
2001118
11
Constitutive activation of the TSH receptor by spontaneous mutations affecting the N‐terminal extracellular domain
FEBS Letters ·Laurence Duprez, Jasmine Parma, Sabine Costagliola, J Hermans, Jacqueline Van Sande, Jacques E. Dumont, Gilbert Vassart
1997118
12
Nephrogenic Syndrome of Inappropriate Antidiuresis in Adults
Journal of the American Society of Nephrology ·Guy Decaux, Frédéric Vandergheynst, Yasmina Bouko, Jasmine Parma, Gilbert Vassart, Catheline Vilain
2007116
13
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia.
The Journal of Clinical Endocrinology & Metabolism ·Massimo Tonacchera, J. Van Sande, Filomena Cetani, S. Swillens, Claire Schvartz, Patrice Winiszewski, Luc Portmann, J.E. Dumont, Gilbert Vassart, Jasmine Parma
1996110
14
Apparent Congenital Athyreosis Contrasting with Normal Plasma Thyroglobulin Levels and Associated with Inactivating Mutations in the Thyrotropin Receptor Gene: Are Athyreosis and Ectopic Thyroid Distinct Entities?1
The Journal of Clinical Endocrinology & Metabolism ·Nellie Gagné, Jasmine Parma, Cole K. Deal, Gilbert Vassart, Guy Van Vliet
1998107
15
Identification and functional characterization of two new somatic mutations causing constitutive activation of the thyrotropin receptor in hyperfunctioning autonomous adenomas of the thyroid.
The Journal of Clinical Endocrinology & Metabolism ·R Paschke, Massimo Tonacchera, J. Van Sande, Jasmine Parma, Gilbert Vassart
1994105
16
A nonsense mutation causes hereditary goitre in the Afrikander cattle and unmasks alternative splicing of thyroglobulin transcripts.
Proceedings of the National Academy of Sciences ·Michael Ricketts, Martijn Simons, Jasmine Parma, Luc Mercken, Q. Dong, Gilbert Vassart
1987100
17
Gene rearrangement and Chernobyl related thyroid cancers
British Journal of Cancer ·Massimo Santoro, G Thomas, Giancarlo Vecchio, G. H. Williams, Alfredo Fusco, Gennaro Chiappetta, V Pozcharskaya, Bogdanova Ti, Eugene P. Demidchik, E. D. Cherstvoy, L Voscoboinik, М.D. Тronko, A. L. Carss, H. Bunnell, M Tonnachera, Jasmine Parma, J.E. Dumont, Gisela Keller, Heinz Höfler, E. D. Williams
200091
18
Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3',5'-monophosphate and inositol phosphate-Ca2+ cascades
Molecular Endocrinology ·Jasmine Parma
199588
19
Characterization of a Novel Loss of Function Mutation of PAX8 in a Familial Case of Congenital Hypothyroidism with In-Place, Normal-Sized Thyroid
The Journal of Clinical Endocrinology & Metabolism ·Laurent Meeus, Brigitte Gilbert, Catherine Rydlewski, Jasmine Parma, Anne Lienhardt Roussie, Marc Abramowicz, Catheline Vilain, Daniel Christophe, Sabine Costagliola, Gilbert Vassart
200486
20
Diversity and Prevalence of Somatic Mutations in the Thyrotropin Receptor and Gs  Genes as a Cause of Toxic Thyroid Adenomas
The Journal of Clinical Endocrinology & Metabolism ·Jasmine Parma
199769

About Jasmine Parma

Jasmine Parma is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology, Genetics, Oncology and Surgery, having authored 66 papers that have together received 4.7k indexed citations. Recurring topics across this work include Thyroid Disorders and Treatments (24 papers), Thyroid Cancer Diagnosis and Treatment (13 papers), Biochemical Analysis and Sensing Techniques (6 papers), interferon and immune responses (5 papers), Growth Hormone and Insulin-like Growth Factors (4 papers), Glycosylation and Glycoproteins Research (3 papers), Congenital heart defects research (3 papers) and RNA and protein synthesis mechanisms (3 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (2.5k citations), Reproductive Medicine (339 citations), Cellular and Molecular Neuroscience (701 citations), Endocrine and Autonomic Systems (230 citations) and Molecular Biology (2.0k citations). Jasmine Parma has collaborated with scholars based in Belgium, France and United States. Frequent co-authors include Gilbert Vassart, Laurence Duprez, Jacqueline Van Sande, Jacques E. Dumont, J. Van Sande, Massimo Tonacchera, Pascale Cochaux, Christine Gervy, Jean Mockel and S. Swillens. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, European Journal of Endocrinology, Journal of Clinical Investigation, Molecular and Cellular Endocrinology and The Journal of Pediatrics.

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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