Patrick Hanna

918 total citations
12 papers, 155 citations indexed

About

Patrick Hanna is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Patrick Hanna has authored 12 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Patrick Hanna's work include Genetic Syndromes and Imprinting (9 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (4 papers). Patrick Hanna is often cited by papers focused on Genetic Syndromes and Imprinting (9 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (4 papers). Patrick Hanna collaborates with scholars based in United States, France and Italy. Patrick Hanna's co-authors include Agnès Linglart, Guiomar Pérez de Nanclares, Giovanna Mantovani, Arrate Pereda, Harald Jüppner, Francesca Marta Elli, Luisa De Sanctis, Virginie Grybek, Elisa Verrua and Bruno Francou and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Clinical Endocrinology & Metabolism and Journal of Bone and Mineral Research.

In The Last Decade

Patrick Hanna

12 papers receiving 155 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrick Hanna United States	6	131	125	13	11	11	12	155
Kaido Lepik Switzerland	6	56 0.4×	77 0.6×	11 0.8×	3 0.3×	4 0.4×	9	141
Pauline Marzin France	7	79 0.6×	62 0.5×	7 0.5×	2 0.2×	6 0.5×	14	120
Hidetoshi Kitajima Japan	4	76 0.6×	50 0.4×	7 0.5×	2 0.2×	5 0.5×	5	125
Ataf Sabir United Kingdom	7	137 1.0×	97 0.8×	15 1.2×	2 0.2×	4 0.4×	19	158
Aisha Al Shamsi United Arab Emirates	6	35 0.3×	67 0.5×	11 0.8×	2 0.2×	4 0.4×	13	129
Rodrick Montjean France	4	66 0.5×	92 0.7×	15 1.2×	3 0.3×	23 2.1×	5	135
Arne Jahn Germany	7	40 0.3×	69 0.6×	17 1.3×	5 0.5×	3 0.3×	19	148
Xiao Bao China	4	45 0.3×	57 0.5×	8 0.6×	2 0.2×	9 0.8×	10	103
Mar Borregán Spain	5	92 0.7×	76 0.6×	10 0.8×	53 4.8×	3 0.3×	11	160
Sergio Daga Italy	6	45 0.3×	66 0.5×	4 0.3×	27 2.5×	7 0.6×	9	120

Countries citing papers authored by Patrick Hanna

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Hanna

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Hanna

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

All Works

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12 of 12 papers shown

Reyes, Monica, Patrick Hanna, Prem Swaroop Yadav, et al.. (2025). A mouse model of Jansen’s metaphyseal chondrodysplasia for investigating disease mechanisms and candidate therapeutics. Proceedings of the National Academy of Sciences. 122(23). e2500176122–e2500176122. 2 indexed citations

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

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

Reyes, Monica, Patrick Hanna, Mohd Golam Quader Khan, et al.. (2023). Substantially Delayed Maturation of Growth Plate Chondrocytes in “Humanized” PTH1R Mice with the H223R Mutation of Jansen's Disease. JBMR Plus. 7(10). e10802–e10802. 5 indexed citations

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

Reyes, Monica, Patrick Hanna, Anu Sharma, et al.. (2021). Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. The Journal of Clinical Endocrinology & Metabolism. 107(2). e681–e687. 6 indexed citations

Reyes, Monica, Patrick Hanna, Serap Turan, et al.. (2021). Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib. The Journal of Clinical Endocrinology & Metabolism. 107(4). e1610–e1619. 5 indexed citations

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

Vlachopapadopoulou, Elpis, et al.. (2020). Pseudohypoparathyroidism type 1B (PHP1B), a rare disorder encountered in adolescence. Journal of Pediatric Endocrinology and Metabolism. 33(11). 1475–1479. 2 indexed citations

10.

Pereda, Arrate, Francesca Marta Elli, Luisa De Sanctis, et al.. (2020). Inactivating PTH/PTHrP signaling disorders (iPPSDs): evaluation of the new classification in a multicenter large series of 544 molecularly characterized patients. European Journal of Endocrinology. 184(2). 311–320. 13 indexed citations

11.

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

12.

Elli, Francesca Marta, Agnès Linglart, Intza Garin, et al.. (2016). The Prevalence of GNAS Deficiency-Related Diseases in a Large Cohort of Patients Characterized by the EuroPHP Network. The Journal of Clinical Endocrinology & Metabolism. 101(10). 3657–3668. 54 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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