Dirk Schnabel

8.1k total citations · 1 hit paper
120 papers, 4.8k citations indexed

About

Dirk Schnabel is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Dirk Schnabel has authored 120 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 34 papers in Endocrinology, Diabetes and Metabolism and 34 papers in Genetics. Recurrent topics in Dirk Schnabel's work include Parathyroid Disorders and Treatments (29 papers), Growth Hormone and Insulin-like Growth Factors (18 papers) and Sexual Differentiation and Disorders (14 papers). Dirk Schnabel is often cited by papers focused on Parathyroid Disorders and Treatments (29 papers), Growth Hormone and Insulin-like Growth Factors (18 papers) and Sexual Differentiation and Disorders (14 papers). Dirk Schnabel collaborates with scholars based in Germany, United States and United Kingdom. Dirk Schnabel's co-authors include Annette Grüters, Heiko Krude, Konrad Sandhoff, Heike Biebermann, Tim M. Strom, Dov Tiosano, Bettina Lorenz‐Depiereux, Maria Schröder, Dieter Haffner and Gabriele Häusler and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Dirk Schnabel

111 papers receiving 4.7k citations

Hit Papers

Clinical practice recommendations for the diagnosis and m... 2019 2026 2021 2023 2019 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dirk Schnabel Germany 36 2.0k 1.4k 1.3k 1.0k 666 120 4.8k
Marie B. Demay United States 41 2.0k 1.0× 1.5k 1.0× 1.1k 0.9× 813 0.8× 544 0.8× 95 7.5k
Yoshiki Seino Japan 39 1.9k 1.0× 1.4k 1.0× 1.1k 0.9× 1.3k 1.2× 507 0.8× 238 6.0k
Yukihiro Hasegawa Japan 31 2.1k 1.1× 1.5k 1.1× 955 0.7× 1.3k 1.2× 330 0.5× 258 5.0k
Matthias Priemel Germany 30 2.1k 1.1× 697 0.5× 393 0.3× 582 0.6× 758 1.1× 76 5.6k
Noriyuki Namba Japan 28 2.8k 1.4× 757 0.5× 536 0.4× 593 0.6× 271 0.4× 100 5.0k
Laurent Beck France 34 1.4k 0.7× 837 0.6× 1.5k 1.1× 234 0.2× 240 0.4× 101 4.5k
Valentin David United States 33 1.4k 0.7× 1.1k 0.8× 1.9k 1.4× 207 0.2× 343 0.5× 66 3.7k
Jon E. Wergedal United States 47 2.9k 1.5× 1.2k 0.8× 329 0.2× 1.3k 1.3× 426 0.6× 109 5.9k
Arthur E. Broadus United States 44 2.6k 1.3× 789 0.5× 1.6k 1.2× 663 0.6× 591 0.9× 93 6.8k
Yosuke Okada Japan 38 2.0k 1.0× 638 0.4× 374 0.3× 1.1k 1.1× 355 0.5× 235 5.0k

Countries citing papers authored by Dirk Schnabel

Since Specialization
Citations

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

Fields of papers citing papers by Dirk Schnabel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dirk Schnabel

This figure shows the co-authorship network connecting the top 25 collaborators of Dirk Schnabel. A scholar is included among the top collaborators of Dirk Schnabel 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 Dirk Schnabel. Dirk Schnabel 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.
Woelfle, Joachim, Dirk Schnabel, & Gerhard Binder. (2024). The treatment of growth disorders in childhood and adolescence. Deutsches Ärzteblatt international. 121(3). 96–106.
2.
Schnabel, Dirk. (2023). Behandlung von komplex chronisch kranken Kindern und Jugendlichen im Sozialpädiatrischen Zentrum (SPZ). Monatsschrift Kinderheilkunde. 171(12). 1062–1070.
4.
Padidela, Raja, Moira Cheung, Jeremy Allgrove, et al.. (2021). BUR-CL207: An Open-label, Multicenter, Non-randomized Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of Burosumab in Pediatric Patients from Birth to Less than 1 Year of Age with XLH.. 94. 1 indexed citations
5.
Meisel, Christian, Tim Meyer, Erwin Lankes, et al.. (2021). Mild COVID-19 despite autoantibodies against type I IFNs in autoimmune polyendocrine syndrome type 1. Journal of Clinical Investigation. 131(14). 55 indexed citations
6.
Padidela, Raja, Ola Nilsson, Outi Mäkitie, et al.. (2020). The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational study. Orphanet Journal of Rare Diseases. 15(1). 172–172. 27 indexed citations
7.
Haffner, Dieter, Francesco Emma, Deborah M. Eastwood, et al.. (2019). Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia. Nature Reviews Nephrology. 15(7). 435–455. 316 indexed citations breakdown →
8.
Coutant, R., et al.. (2018). Year-one Effectiveness and Overall Safety of NutropinAq® for Growth Hormone Deficiency (GHD) and Other Paediatric Growth Disorders: Completion of the International Cooperative Growth Study (iNCGS) European Registry. 1 indexed citations
9.
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
10.
Schnabel, Dirk, et al.. (2018). Transient Simulation of Cooling-Lubricant Flow for Deep-Hole Drilling-Processes. Procedia CIRP. 77. 78–81. 8 indexed citations
11.
Haffner, Dieter, Hagen Staude, Elke Wühl, et al.. (2017). Effects of growth hormone treatment on adult height in severely short children with X-linked hypophosphatemic rickets. Pediatric Nephrology. 33(3). 447–456. 31 indexed citations
12.
Mayr, B, Dirk Schnabel, Helmuth‐Günther Dörr, & Christof Schöfl. (2015). GENETICS IN ENDOCRINOLOGY: Gain and loss of function mutations of the calcium-sensing receptor and associated proteins: current treatment concepts. European Journal of Endocrinology. 174(5). R189–R208. 44 indexed citations
14.
Korvala, Johanna, Harald Jüppner, Outi Mäkitie, et al.. (2012). Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity. BMC Medical Genetics. 13(1). 26–26. 85 indexed citations
15.
Alatzoglou, Kyriaki S., Christopher T. Cowell, Rodger Palmer, et al.. (2011). Increased Transactivation Associated with SOX3 Polyalanine Tract Deletion in a Patient with Hypopituitarism. Molecular Endocrinology. 25(3). 546–546. 3 indexed citations
16.
Lorenz‐Depiereux, Bettina, Dirk Schnabel, Dov Tiosano, Gabriele Häusler, & Tim M. Strom. (2010). Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets. The American Journal of Human Genetics. 86(2). 267–272. 261 indexed citations
17.
Živičnjak, Miroslav, Dirk Schnabel, Heiko Billing, et al.. (2010). Age-related stature and linear body segments in children with X-linked hypophosphatemic rickets. Pediatric Nephrology. 26(2). 223–231. 63 indexed citations
19.
Lorenz‐Depiereux, Bettina, Anna Benet‐Pagès, Gertrud Eckstein, et al.. (2006). Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3. The American Journal of Human Genetics. 78(2). 193–201. 252 indexed citations
20.
Krude, Heiko, et al.. (2004). The Use of L-T4 as Liquid Solution Improves the Practicability and Individualized Dosage in Newborns and Infants with Congenital Hypothyroidism. Journal of Pediatric Endocrinology and Metabolism. 17(7). 967–74. 23 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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