H Stobbe

1.1k total citations
45 papers, 841 citations indexed

About

H Stobbe is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, H Stobbe has authored 45 papers receiving a total of 841 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in H Stobbe's work include Growth Hormone and Insulin-like Growth Factors (9 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Genetic Syndromes and Imprinting (4 papers). H Stobbe is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (9 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Genetic Syndromes and Imprinting (4 papers). H Stobbe collaborates with scholars based in Germany, United States and Türkiye. H Stobbe's co-authors include Werner Blum, Marco Ramadani, Bettina Rau, Frank Gansauge, H. G. Beger, Susanne Gansauge, Roland Pfaeffle, Roland Pfäffle, Alexandra Keller and Johannes Weigel and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Clinical Endocrinology.

In The Last Decade

H Stobbe

40 papers receiving 804 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H Stobbe Germany 11 377 359 252 193 122 45 841
M Goossens France 6 332 0.9× 322 0.9× 174 0.7× 87 0.5× 72 0.6× 9 640
B. M. J. Stringer United Kingdom 13 312 0.8× 475 1.3× 164 0.7× 287 1.5× 81 0.7× 32 926
Florence Dastot France 16 385 1.0× 764 2.1× 487 1.9× 73 0.4× 117 1.0× 19 1.0k
Cora Groffen Netherlands 13 357 0.9× 484 1.3× 138 0.5× 35 0.2× 130 1.1× 16 766
KEIICHI MATSUO United States 13 405 1.1× 737 2.1× 221 0.9× 507 2.6× 134 1.1× 15 1.1k
Patricia A. Short United States 11 451 1.2× 398 1.1× 146 0.6× 39 0.2× 80 0.7× 15 808
Susanne V. Allander Sweden 12 302 0.8× 188 0.5× 99 0.4× 140 0.7× 115 0.9× 18 728
Caroline Buckway United States 12 323 0.9× 627 1.7× 304 1.2× 134 0.7× 86 0.7× 16 891
Jean-Paul Beressi France 11 316 0.8× 460 1.3× 553 2.2× 71 0.4× 52 0.4× 20 1.2k
Ifat Geron United States 13 591 1.6× 186 0.5× 225 0.9× 117 0.6× 146 1.2× 25 1.0k

Countries citing papers authored by H Stobbe

Since Specialization
Citations

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

Fields of papers citing papers by H Stobbe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Stobbe

This figure shows the co-authorship network connecting the top 25 collaborators of H Stobbe. A scholar is included among the top collaborators of H Stobbe 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 H Stobbe. H Stobbe 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.
Klammt, Jürgen, David Neumann, Shayne F. Andrew, et al.. (2014). Severe Short Stature and GH Insensitivity Due to a De Novo Heterozygous STAT5B Missense Mutation. 82. 1 indexed citations
2.
Flemming, Gunter, Jürgen Klammt, Geoffrey Ambler, et al.. (2013). Functional Characterization of a Heterozygous GLI2 Missense Mutation in Patients With Multiple Pituitary Hormone Deficiency. The Journal of Clinical Endocrinology & Metabolism. 98(3). E567–E575. 28 indexed citations
3.
Binder, Gerhard, Wieland Kieß, Monique Losekoot, et al.. (2013). Alu-Mediated Recombination Defect in IGF1R: Haploinsufficiency in a Patient with Short Stature. Hormone Research in Paediatrics. 80(6). 431–442. 7 indexed citations
4.
Durmaz, Burak, et al.. (2011). A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies. Journal of Pediatric Endocrinology and Metabolism. 24(9-10). 779–82. 6 indexed citations
5.
Gucev, Zoran, Velibor Tasić, H Stobbe, et al.. (2011). A Novel GH1 Mutation in a Family with Isolated Growth Hormone Deficiency Type II. Hormone Research in Paediatrics. 77(3). 200–204. 4 indexed citations
6.
Lebl, Jan, Roland Pfaeffle, H Stobbe, et al.. (2005). Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects. European Journal of Endocrinology. 153(3). 389–396. 45 indexed citations
7.
8.
Böttner, A, Eberhard Keller, H Stobbe, et al.. (2004). PROP1Mutations Cause Progressive Deterioration of Anterior Pituitary Function including Adrenal Insufficiency: A Longitudinal Analysis. The Journal of Clinical Endocrinology & Metabolism. 89(10). 5256–5265. 97 indexed citations
9.
Crone, Julia, et al.. (2002). Familial Combined Pituitary Hormone Deficiency Caused by <i>PROP-1</i> Gene Mutation. Hormone Research in Paediatrics. 57(3-4). 120–126. 17 indexed citations
10.
Elstner, Elena, et al.. (1985). Stromal Progenitor Cells in Bone Marrow of Patients with Aplastic Anemia. Hämatologie und Bluttransfusion. 29. 168–171. 4 indexed citations
11.
Stobbe, H, et al.. (1985). [Cytogenetic findings in chronic myelogenous leukemia].. PubMed. 112(4). 495–514. 1 indexed citations
12.
Stobbe, H. (1981). [Risk factor benzene (author's transl)].. PubMed. 51(7). 575–8.
13.
Stobbe, H, et al.. (1969). Lymphozytentransformationstest bei chronischer lymphatischer Leukose unter Berücksichtigung der absoluten Lymphozytenzahl im Blut. Acta Haematologica. 41(3). 144–153. 2 indexed citations
14.
Stobbe, H, et al.. (1968). [Lymphocyte stimulation in Hodgkin's disease in the tissue culture].. PubMed. 23(1). 32–3. 1 indexed citations
15.
Stobbe, H, et al.. (1968). Untersuchungen zur Korrelation von Lymphozyten- transformation durch Streptolysin 0 in vitro und Antistreptolysintiter. Acta Haematologica. 39(5). 276–281. 2 indexed citations
16.
Stobbe, H, et al.. (1966). [On the occurrence of fetal hemoglobin in acquired blood diseases].. PubMed. 96(38). 1269–72. 1 indexed citations
17.
Stobbe, H. (1958). [Structural elements of plasma cells].. PubMed. 2(3). 305–16. 2 indexed citations
18.
Stobbe, H. (1958). [Changes in gastrointestinal system in leukemia].. PubMed. 53(13). 497–9. 3 indexed citations
19.
Stobbe, H. (1955). [Gamma globulin deficiency and lowered resistance to infection; clinical studies on hypo- and agammaglobulinemia].. PubMed. 10(22). 1040–6. 1 indexed citations
20.
Stobbe, H. (1954). [The islands of Langerhans in pancreatic carcinoma].. PubMed. 9(18). 917–8. 1 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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