Harald Jüppner

24.2k total citations · 5 hit papers
240 papers, 15.2k citations indexed

About

Harald Jüppner is a scholar working on Molecular Biology, Nephrology and Oncology. According to data from OpenAlex, Harald Jüppner has authored 240 papers receiving a total of 15.2k indexed citations (citations by other indexed papers that have themselves been cited), including 115 papers in Molecular Biology, 96 papers in Nephrology and 95 papers in Oncology. Recurrent topics in Harald Jüppner's work include Bone health and treatments (94 papers), Parathyroid Disorders and Treatments (94 papers) and Genetic Syndromes and Imprinting (62 papers). Harald Jüppner is often cited by papers focused on Bone health and treatments (94 papers), Parathyroid Disorders and Treatments (94 papers) and Genetic Syndromes and Imprinting (62 papers). Harald Jüppner collaborates with scholars based in United States, Germany and France. Harald Jüppner's co-authors include Clemens Bergwitz, Abdul‐Badi Abou‐Samra, Thomas J. Gardella, Henry M. Kronenberg, Ernestina Schipani, Murat Bastepe, Kenneth B. Jonsson, Östen Ljunggren, Isidro B. Salusky and John T. Potts and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Harald Jüppner

231 papers receiving 14.8k citations

Hit Papers

PTH/PTHrP Receptor in Early Development and Indian Hedgeh... 1992 2026 2003 2014 1996 1992 2003 2003 2010 250 500 750 1000
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.

  1. PTH/PTHrP Receptor in Early Development and Indian Hedgehog—Regulated Bone Growth
    1996 1.0k citations Harald Jüppner et al. profile →
  2. Expression cloning of a common receptor for parathyroid hormone and parathyroid hormone-related peptide from rat osteoblast-like cells: a single receptor stimulates intracellular accumulation of both cAMP and inositol trisphosphates and increases intracellular free calcium.
    1992 817 citations Harald Jüppner, John T. Potts et al. Proceedings of the National Academy of Sciences profile →
  3. Fibroblast Growth Factor 23 in Oncogenic Osteomalacia and X-Linked Hypophosphatemia
    2003 683 citations Kenneth B. Jonsson, Kenneth E. White et al. profile →
  4. Circulating concentration of FGF-23 increases as renal function declines in patients with chronic kidney disease, but does not change in response to variation in phosphate intake in healthy volunteers
    2003 544 citations Östen Ljunggren, Harald Jüppner et al. profile →
  5. Regulation of Phosphate Homeostasis by PTH, Vitamin D, and FGF23
    2010 496 citations Clemens Bergwitz, Harald Jüppner profile →

Peers

Harald Jüppner
Seiji Fukumoto Japan
Beate Lanske United States
Michael J. Econs United States
Takeyoshi Yamashita Japan
Stephen J. Marx United States
Geoffrey N. Hendy Canada
Michael P. Whyte United States
Andrew C. Karaplis Canada
Gino V. Segre United States
Shiguang Liu United States
Seiji Fukumoto Japan
Harald Jüppner
Citations per year, relative to Harald Jüppner Harald Jüppner (= 1×) peers Seiji Fukumoto

Countries citing papers authored by Harald Jüppner

Since Specialization
Citations

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

Fields of papers citing papers by Harald Jüppner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harald Jüppner

This figure shows the co-authorship network connecting the top 25 collaborators of Harald Jüppner. A scholar is included among the top collaborators of Harald Jüppner 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 Harald Jüppner. Harald Jüppner 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.
Reyes, Monica, Barbara Gales, Agnès Linglart, et al.. (2025). Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B. Proceedings of the National Academy of Sciences. 122(16). e2423271122–e2423271122. 2 indexed citations
2.
Reyes, Monica, et al.. (2025). A biallelically active embryonic enhancer dictates GNAS imprinting through allele-specific conformations. Nature Communications. 16(1). 1377–1377. 1 indexed citations
3.
Calder, Alistair, Jeremy Allgrove, Moira Cheung, et al.. (2024). Eiken syndrome with parathyroid hormone resistance due to a novel parathyroid hormone receptor type 1 mutation: clinical features and functional analysis. Journal of Bone and Mineral Research. 39(11). 1596–1605. 3 indexed citations
4.
Liu, Shi, Lauren My-Linh Tran, Zhen Yu, et al.. (2024). Backbone Modification Provides a Long-Acting Inverse Agonist of Pathogenic, Constitutively Active PTH1R Variants. Journal of the American Chemical Society. 146(10). 6522–6529. 2 indexed citations
5.
Nozu, Kandai, et al.. (2023). Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II. JCEM Case Reports. 1(2). luad019–luad019.
6.
Zhou, Wen, Eva S. Liu, Sherri‐Ann M. Burnett‐Bowie, et al.. (2023). 1,25-Dihydroxyvitamin D3 regulates furin-mediated FGF23 cleavage. JCI Insight. 8(17). 9 indexed citations
7.
Nanclares, Guiomar Pérez de, Harald Jüppner, Patrick Hanna, et al.. (2023). Recombinant growth hormone improves growth and adult height in patients with maternal inactivating GNAS mutations. European Journal of Endocrinology. 189(1). 123–131. 3 indexed citations
8.
Hanna, Patrick, Ashok Khatri, Séverine Brabant, et al.. (2023). Homozygous Ser-1 to Pro-1 mutation in parathyroid hormone identified in hypocalcemic patients results in secretion of a biologically inactive pro-hormone. Proceedings of the National Academy of Sciences. 120(8). e2208047120–e2208047120. 3 indexed citations
9.
Hanna, Patrick, Bruno Francou, Brigitte Delemer, Harald Jüppner, & Agnès Linglart. (2021). A Novel Familial PHP1B Variant With Incomplete Loss of Methylation at GNAS-A/B and Enhanced Methylation at GNAS-AS2. The Journal of Clinical Endocrinology & Metabolism. 106(9). 2779–2787. 7 indexed citations
10.
Miller, Danny E., Patrick Hanna, Monica Reyes, et al.. (2020). Targeted Long-Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b (PHP1B). Journal of Bone and Mineral Research. 37(9). 1711–1719. 19 indexed citations
11.
Biebermann, Heike, Gunnar Kleinau, Dirk Schnabel, et al.. (2018). A New Multisystem Disorder Caused by the Gαs Mutation p.F376V. The Journal of Clinical Endocrinology & Metabolism. 104(4). 1079–1089. 10 indexed citations
12.
Li, Yuwen, Daniel Caballero, Chuanlong Zhu, et al.. (2017). Response of Npt2a knockout mice to dietary calcium and phosphorus. PLoS ONE. 12(4). e0176232–e0176232. 15 indexed citations
13.
Glorieux, Francis H., John Μ. Pettifor, & Harald Jüppner. (2011). Pediatric bone : biology & diseases. 25 indexed citations
14.
Mannstadt, Michael, Guylène Bertrand, Mihaela Mureşan, et al.. (2008). Dominant-Negative GCMB Mutations Cause an Autosomal Dominant Form of Hypoparathyroidism. The Journal of Clinical Endocrinology & Metabolism. 93(9). 3568–3576. 53 indexed citations
15.
Wesseling‐Perry, Katherine, Renata C. Pereira, Hong Wang, et al.. (2008). Relationship between Plasma Fibroblast Growth Factor-23 Concentration and Bone Mineralization in Children with Renal Failure on Peritoneal Dialysis. The Journal of Clinical Endocrinology & Metabolism. 94(2). 511–517. 117 indexed citations
16.
Bergwitz, Clemens, Nicole M. Roslin, Martin Tieder, et al.. (2006). SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis. The American Journal of Human Genetics. 78(2). 179–192. 324 indexed citations
17.
John, Markus R., Maya Arai, David A. Rubin, Kenneth B. Jonsson, & Harald Jüppner. (2002). Identification and Characterization of the Murine and Human Gene Encoding the Tuberoinfundibular Peptide of 39 Residues. Endocrinology. 143(3). 1047–1057. 33 indexed citations
18.
White, Kenneth E., Kenneth B. Jonsson, Gwénaëlle Carn, et al.. (2001). The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate Wasting. The Journal of Clinical Endocrinology & Metabolism. 86(2). 497–500. 231 indexed citations
19.
Li, Yan Chun, Clemens Bergwitz, Harald Jüppner, & Marie B. Demay. (1997). Cloning and Characterization of the Vitamin D Receptor from Xenopus laevis*. Endocrinology. 138(6). 2347–2353. 40 indexed citations
20.
Maeda, Shintaro, S. Vincent Wu, Harald Jüppner, et al.. (1996). Cell-specific signal transduction of parathyroid hormone (PTH)-related protein through stably expressed recombinant PTH/PTHrP receptors in vascular smooth muscle cells.. Endocrinology. 137(8). 3154–3162. 53 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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