Harald Jüppner

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 18 papers. Top paper: “Glycerol-3-phosphate is an FGF23 regulator derived from the injured kidney”.

Glycerol-3-phosphate is an FGF23 regulator derived from the injured kidney

Journal of Clinical Investigation(2020)10.1172/jci131190

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0DataRank · unranked

124 citations

Wondong Kim, Wen Zhou, Kerry A. Pierce, Wenhan Chang, David B. Sykes +20 more

Nephropathic Cystinosis: A Distinct Form of CKD–Mineral and Bone Disorder that Provides Novel Insights into the Regulation of FGF23

Journal of the American Society of Nephrology(2020)10.1681/asn.2019111172

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0DataRank · unranked

22 citations

Macarena Jiménez, Carlos R. Ferreira, Galina Nesterova, Mary Scott Roberts, Sri Harsha Tella +11 more

Actions of Parathyroid Hormone Ligand Analogues in Humanized PTH1R Knockin Mice

Endocrinology(2022)10.1210/endocr/bqac054

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0DataRank · unranked

12 citations

Sung-Hee Yoon, Monica Reyes, Michael Bruce, Daniel J. Brooks, Mary Bouxsein +7 more

Functional Properties of Two Distinct PTH1R Mutants Associated With Either Skeletal Defects or Pseudohypoparathyroidism

JBMR Plus(2022)10.1002/jbm4.10604

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6 citations

Thomas Dean, Ashok Khatri, Harald Jüppner, Thomas J. Gardella, Ignacio Portales‐Castillo

Kidney glycolysis serves as a mammalian phosphate sensor that maintains phosphate homeostasis

Journal of Clinical Investigation(2023)10.1172/jci164610

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0DataRank · unranked

74 citations

Petra Šimić, Iris Y. Zhou, Peter Caravan, Xavier Vela Parada, Donghai Wen +10 more

Altered Signaling and Desensitization Responses in PTH1R Mutants Associated with Eiken Syndrome

Communications Biology(2023)10.1038/s42003-023-04966-0

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0DataRank · unranked

14 citations

Thomas Dean, Ross W. Cheloha, Brendan A. Creemer, Jean‐Pierre Vilardaga, Sofya Savransky +4 more

1,25-Dihydroxyvitamin D3 regulates furin-mediated FGF23 cleavage

JCI Insight(2023)10.1172/jci.insight.168957

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0DataRank · unranked

14 citations

Isinsu Bastepe, Wen Zhou, Birol Ay, Zara Ceraj, Ignacio Portales‐Castillo +7 more

Substantially Delayed Maturation of Growth Plate Chondrocytes in “Humanized” PTH1R Mice with the H223R Mutation of Jansen's Disease

JBMR Plus(2023)10.1002/jbm4.10802

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0DataRank · unranked

11 citations

Damla Firat, Patrick Hanna, Mohd Golam Quader Khan, Michael Bruce, Maria Shvedova +5 more

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(2023)10.1073/pnas.2208047120

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0DataRank · unranked

6 citations

Ashok Khatri, Shawn Choi, Séverine Brabant, Matti L. Gild, Marie Piketty +8 more

Pseudohypoparathyroidism: complex disease variants with unfortunate names

Journal of Molecular Endocrinology(2023)10.1530/jme-23-0104

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0DataRank · unranked

8 citations

Harald Jüppner

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(2024)10.1093/jbmr/zjae148

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0DataRank · unranked

4 citations

Jeremy Allgrove, Jakob Höppner, Moira Cheung, Saji Alexander, Lorenzo Garagnani +5 more

Backbone Modification Provides a Long-Acting Inverse Agonist of Pathogenic, Constitutively Active PTH1R Variants

Journal of the American Chemical Society(2024)10.1021/jacs.3c09694

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0DataRank · unranked

5 citations

Eileen J. Daley, Lauren My-Linh Tran, Zhen Yu, Monica Reyes, Thomas Dean +8 more

GNAS AS2 methylation status enables mechanism-based categorization of pseudohypoparathyroidism type 1B

JCI Insight(2024)10.1172/jci.insight.177190

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3 citations

Monica Reyes, Harald Jüppner, Murat Bastepe, Yorihiro Iwasaki

Reduced guanidinoacetate in plasma of patients with autosomal dominant Fanconi syndrome due to heterozygous P341L GATM variant and study of organoids towards treatment

JIMD Reports(2024)10.1002/jmd2.12442

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0DataRank · unranked

1 citations

R. Singal, Anastasia Ambrose, Jong Hee Song, Minsoo Son, Young Ah Goo +11 more

Jansen metaphyseal chondrodysplasia: analysis of craniofacial manifestations

JBMR Plus(2024)10.1093/jbmrpl/ziae156

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0DataRank · unranked

0 citations

Konstantinia Almpani, Hung Jeffrey Kim, Christopher Zalewski, Emily Y. Chu, Golnar Jahanmir +11 more

A biallelically active embryonic enhancer dictates GNAS imprinting through allele-specific conformations

Nature Communications(2025)10.1038/s41467-025-56608-0

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0DataRank · unranked

3 citations

Monica Reyes, Harald Jüppner, Murat Bastepe, Yorihiro Iwasaki

Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2423271122

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0DataRank · unranked

3 citations

Monica Reyes, Anna Ryabets‐Lienhard, Barbara Gales, Agnès Linglart, Danny E. Miller +4 more

Jansen's Disease: Bone Abnormalities Beyond Chondrodysplasia

The Journal of Clinical Endocrinology & Metabolism(2025)10.1210/clinem/dgaf097

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0DataRank · unranked

0 citations

Anne M. Delany, Monica Reyes, Barbara Gales, Harald Jüppner, Isidro B. Salusky +1 more