Pia Hermanns

1.4k total citations
41 papers, 994 citations indexed

About

Pia Hermanns is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Pia Hermanns has authored 41 papers receiving a total of 994 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 13 papers in Endocrinology, Diabetes and Metabolism and 12 papers in Genetics. Recurrent topics in Pia Hermanns's work include Thyroid Disorders and Treatments (13 papers), Congenital heart defects research (10 papers) and RNA modifications and cancer (6 papers). Pia Hermanns is often cited by papers focused on Thyroid Disorders and Treatments (13 papers), Congenital heart defects research (10 papers) and RNA modifications and cancer (6 papers). Pia Hermanns collaborates with scholars based in Germany, United States and United Kingdom. Pia Hermanns's co-authors include Bernhard Zabel, Joachim Pohlenz, Jörg Schirrmeister, Brendan Lee, Samuel Refetoff, Brendan Lee, Helmut Grasberger, Markus Jörg Altenburger, Terry Bertin and Chad A. Shaw and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Pia Hermanns

39 papers receiving 973 citations

Peers

Pia Hermanns
James Thompson Finland
Elizabeth H. Holt United States
Frances Connor Australia
Laleh Ardeshirpour United States
Pamela S. Karnes United States
Gary L. Schechter United States
Margareta Behrendt Sweden
Zeynep Coban‐Akdemir United States
Pei-Chin Chuang Taiwan
Irfan Saadi United States
James Thompson Finland
Pia Hermanns
Citations per year, relative to Pia Hermanns Pia Hermanns (= 1×) peers James Thompson

Countries citing papers authored by Pia Hermanns

Since Specialization
Citations

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

Fields of papers citing papers by Pia Hermanns

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pia Hermanns

This figure shows the co-authorship network connecting the top 25 collaborators of Pia Hermanns. A scholar is included among the top collaborators of Pia Hermanns 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 Pia Hermanns. Pia Hermanns 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.
Choukair, Daniela, Philipp Vick, Pia Hermanns, et al.. (2020). Identification of <b><i>Transient Receptor Potential Channel 4-Associated Protein</i></b> as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism. Hormone Research in Paediatrics. 93(1). 16–29. 10 indexed citations
2.
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Kharbanda, Mira, Pia Hermanns, Jeremy Jones, et al.. (2017). A further case of brain-lung-thyroid syndrome with deletion proximal to NKX2-1. European Journal of Medical Genetics. 60(5). 257–260. 13 indexed citations
4.
5.
Winter, Julia, Olaf Hiort, Pia Hermanns, Susanne Thiele, & Joachim Pohlenz. (2011). A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones. Journal of Pediatric Endocrinology and Metabolism. 24(5-6). 297–301. 2 indexed citations
6.
Hermanns, Pia, Helmut Grasberger, Samuel Refetoff, & Joachim Pohlenz. (2011). Mutations in the NKX2.5 Gene and the PAX8 Promoter in a Girl with Thyroid Dysgenesis. The Journal of Clinical Endocrinology & Metabolism. 96(6). E977–E981. 28 indexed citations
7.
Hulur, Imge, Pia Hermanns, Sabine Heger, et al.. (2011). A Single Copy of the Recently Identified Dual Oxidase Maturation Factor (DUOXA) 1 Gene Produces Only Mild Transient Hypothyroidism in a Patient with a Novel Biallelic DUOXA2 Mutation and Monoallelic DUOXA1 Deletion. The Journal of Clinical Endocrinology & Metabolism. 96(5). E841–E845. 46 indexed citations
8.
Mattijssen, Sandy, Ella R. Hinson, Carla Onnekink, et al.. (2010). Viperin mRNA is a novel target for the human RNase MRP/RNase P endoribonuclease. Cellular and Molecular Life Sciences. 68(14). 2469–2480. 27 indexed citations
9.
Mari, Francesca, Pia Hermanns, F. Galluzzi, et al.. (2009). Refinement of the 12q14 microdeletion syndrome: primordial dwarfism and developmental delay with or without osteopoikilosis. European Journal of Human Genetics. 17(9). 1141–1147. 27 indexed citations
10.
Lausch, Ekkehart, Pia Hermanns, Henner F. Farin, et al.. (2008). TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome. The American Journal of Human Genetics. 83(5). 649–655. 46 indexed citations
11.
Conwell, Louise S., Pia Hermanns, & Andreas Zankl. (2008). Short Stature and Metaphyeal Dysplasia Due to Cartilage-Hair Hypoplasia. Journal of Pediatric Endocrinology and Metabolism. 21(3). 209–11. 5 indexed citations
12.
Morello, Roy, Terry Bertin, Silke Schlaubitz, et al.. (2008). Brachy–syndactyly caused by loss of Sfrp2 function. Journal of Cellular Physiology. 217(1). 127–137. 56 indexed citations
13.
14.
Schirrmeister, Jörg, et al.. (2006). Detectability of residual Epiphany and gutta‐percha after root canal retreatment using a dental operating microscope and radiographs – an ex vivo study. International Endodontic Journal. 39(7). 558–565. 71 indexed citations
15.
Tagariello, Andreas, Silke Schlaubitz, Thomas Hankeln, et al.. (2005). Expression profiling of human fetal growth plate cartilage by EST sequencing. Matrix Biology. 24(8). 530–538. 11 indexed citations
16.
Hermanns, Pia, Alison A. Bertuch, Terry Bertin, et al.. (2005). Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia. Human Molecular Genetics. 14(23). 3723–3740. 86 indexed citations
17.
Mendoza‐Londono, Roberto, Edward J. Lammer, Rosemarie Watson, et al.. (2005). Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS. The American Journal of Human Genetics. 77(1). 161–168. 13 indexed citations
18.
Curry, Stacey, et al.. (2004). Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador. Ophthalmic Genetics. 25(1). 3–9. 25 indexed citations
19.
Bateman, John F., Susanna Freddi, Robyn McNeil, et al.. (2004). Identification of four novel COL10A1 missense mutations in schmid metaphyseal chondrodysplasia: Further evidence that collagen X NC1 mutations impair trimer assembly. Human Mutation. 23(4). 396–396. 18 indexed citations
20.
Hermanns, Pia & Brendan Lee. (2001). Transcriptional dysregulation in skeletal malformation syndromes. American Journal of Medical Genetics. 106(4). 258–271. 22 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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