H Wollmann

2.7k total citations
88 papers, 1.9k citations indexed

About

H Wollmann is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, H Wollmann has authored 88 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Pediatrics, Perinatology and Child Health, 39 papers in Molecular Biology and 37 papers in Genetics. Recurrent topics in H Wollmann's work include Genetic Syndromes and Imprinting (30 papers), Growth Hormone and Insulin-like Growth Factors (21 papers) and Prenatal Screening and Diagnostics (20 papers). H Wollmann is often cited by papers focused on Genetic Syndromes and Imprinting (30 papers), Growth Hormone and Insulin-like Growth Factors (21 papers) and Prenatal Screening and Diagnostics (20 papers). H Wollmann collaborates with scholars based in Germany, United States and United Kingdom. H Wollmann's co-authors include Michael B. Ranke, Thomas Eggermann, Gerhard Binder, Katja Eggermann, Roland Schweizer, C. P. Schwarze, Meinolf Noeker, Peter Kaiser, Karin Weber and John Eric Chaplin and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PEDIATRICS and Human Molecular Genetics.

In The Last Decade

H Wollmann

86 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H Wollmann Germany	25	1.0k	785	769	766	220	88	1.9k
Helmuth G. Dörr Germany	27	543 0.5×	1.1k 1.4×	1.1k 1.5×	489 0.6×	209 0.9×	141	2.4k
Claudine Heinrichs Belgium	30	614 0.6×	1.1k 1.4×	1.1k 1.4×	907 1.2×	65 0.3×	88	2.6k
Neus Potau Spain	33	1.6k 1.5×	1.9k 2.4×	818 1.1×	323 0.4×	666 3.0×	82	4.2k
Ina Knerr Germany	29	571 0.6×	316 0.4×	808 1.1×	425 0.6×	339 1.5×	110	2.5k
J. J. J. Waelkens Netherlands	22	357 0.3×	811 1.0×	580 0.8×	363 0.5×	88 0.4×	40	1.5k
Clara Pariente Israel	24	437 0.4×	574 0.7×	426 0.6×	150 0.2×	325 1.5×	56	2.6k
Joan DiMartino-Nardi United States	23	335 0.3×	926 1.2×	476 0.6×	246 0.3×	86 0.4×	40	1.6k
María Victoria Marcos Spain	26	956 0.9×	842 1.1×	393 0.5×	125 0.2×	455 2.1×	34	2.3k
Arturo Zárate Mexico	26	296 0.3×	758 1.0×	324 0.4×	214 0.3×	310 1.4×	216	2.1k
G. Massa Belgium	26	343 0.3×	622 0.8×	745 1.0×	772 1.0×	28 0.1×	77	1.8k

Countries citing papers authored by H Wollmann

Since Specialization

Citations

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

Fields of papers citing papers by H Wollmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Wollmann

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bakker, Nienke, et al.. (2017). Growth Hormone Treatment in Children With Prader-Willi Syndrome: Three Years of Longitudinal Data in Prepubertal Children and Adult Height Data From the KIGS Database. The Journal of Clinical Endocrinology & Metabolism. 102(5). 1702–1711. 35 indexed citations

Bullinger, Monika, Julia Quitmann, Mick Power, et al.. (2013). Assessing the quality of life of health-referred children and adolescents with short stature: development and psychometric testing of the QoLISSY instrument. Health and Quality of Life Outcomes. 11(1). 76–76. 60 indexed citations

Kaspers, Stefan, Michael B. Ranke, Jane Loftus, et al.. (2013). Implications of a Data-Driven Approach to Treatment with Growth Hormone in Children with Growth Hormone Deficiency and Turner Syndrome. Applied Health Economics and Health Policy. 11(3). 237–249. 14 indexed citations

Ranke, Michael B., Anders Lindberg, Stefan Kaspers, et al.. (2012). Accurate Long-Term Prediction of Height during the First Four Years of Growth Hormone Treatment in Prepubertal Children with Growth Hormone Deficiency or Turner Syndrome. Hormone Research in Paediatrics. 78(1). 8–17. 15 indexed citations

Ranke, Michael B., David Martín, Stefan Ehehalt, et al.. (2011). Short Children with Low Birth Weight Born either Small for Gestational Age or Average for Gestational Age Show Similar Growth Response and Changes in Insulin-Like Growth Factor-1 to Growth Hormone Treatment during the First Prepubertal Year. Hormone Research in Paediatrics. 76(2). 104–112. 6 indexed citations

Bullinger, Monika, Maria Kołtowska‐Häggström, David E. Sandberg, et al.. (2009). Health-Related Quality of Life of Children and Adolescents with Growth Hormone Deficiency or Idiopathic Short Stature – Part 2: Available Results and Future Directions. Hormone Research in Paediatrics. 72(2). 74–81. 56 indexed citations

Eggermann, Katja, Nadine Schönherr, Michael B. Ranke, et al.. (2008). Search for Subtelomeric Imbalances by Multiplex Ligation-Dependent Probe Amplification in Silver–Russell Syndrome. Genetic Testing. 12(1). 111–113. 2 indexed citations

Schönherr, Nadine, Esther Meyer, Katja Eggermann, et al.. (2006). (Epi)mutations in 11p15 significantly contribute to Silver–Russell syndrome: but are they generally involved in growth retardation?. European Journal of Medical Genetics. 49(5). 414–418. 38 indexed citations

Meyer, Esther, et al.. (2004). Searching for genomic variants in IGF2 and CDKN1C in Silver–Russell syndrome patients. Molecular Genetics and Metabolism. 82(3). 246–250. 16 indexed citations

10.

Wollmann, H, et al.. (2003). Characterization of Genomic Variants in CSH1 and GH2 , Two Candidate Genes for Silver-Russell Syndrome in 17q24-q25. Genetic Testing. 7(3). 259–263. 16 indexed citations

11.

Eggermann, Thomas, Klaus Zerres, Katja Eggermann, Gudrun E. Moore, & H Wollmann. (2002). Uniparental disomy: clinical indications for testing in growth retardation. European Journal of Pediatrics. 161(6). 305–312. 18 indexed citations

12.

Mergenthaler, Susanne, Andrew J. Sharp, Michael B. Ranke, et al.. (2001). Gene Dosage Analysis in Silver-Russell Syndrome: Use of Quantitative Competitive PCR and Dual-Color FISH to Estimate the Frequency of Duplications in 7p11.2–p13. Genetic Testing. 5(3). 261–266. 9 indexed citations

13.

Ranke, Michael B., Roland Schweizer, Martin W. Elmlinger, et al.. (2001). Relevance of IGF-I, IGFBP-3, and IGFBP-2 Measurements during GH Treatment of GH-Deficient and Non-GH-Deficient Children and Adolescents. Hormone Research in Paediatrics. 55(3). 115–124. 61 indexed citations

14.

Eggermann, Katja, H Wollmann, Jürgen Tomiuk, et al.. (1999). Screening for Mutations in the Promoter and the Coding Region of the IGFBP1 and IGFBP3 Genes in Silver-Russell Syndrome Patients. Human Heredity. 49(3). 123–128. 19 indexed citations

15.

Wollmann, H. (1998). Intrauterine Growth Restriction: Definition and Etiology. Hormone Research in Paediatrics. 49(Suppl. 2). 1–6. 190 indexed citations

16.

Strasser-Wozak, Elisabeth MC, et al.. (1997). CYP11B1 Mutations Causing Non-Classic Adrenal Hyperplasia due to 11 -Hydroxylase Deficiency. Human Molecular Genetics. 6(11). 1829–1834. 88 indexed citations

17.

Wollmann, H, et al.. (1995). Dose-Dependent Responses in Insulin-Like Growth Factors, Insulin-Like Growth Factor-Binding Protein-3 and Parameters of Bone Metabolism to Growth Hormone Therapy in Young Adults with Growth Hormone Deficiency. Hormone Research. 43(6). 249–256. 10 indexed citations

18.

Wollmann, H, Uwe Pleyer, Sabine Friedel, et al.. (1994). Neuroendocrine alterations in uveitis patients. Graefe s Archive for Clinical and Experimental Ophthalmology. 232(5). 297–301. 5 indexed citations

19.

Reimann, I. W., et al.. (1987). Influence of oestradiol on alpha2-adrenoceptor binding sites on intact platelets of young male volunteers. European Journal of Clinical Pharmacology. 33(2). 147–150. 2 indexed citations

20.

Wollmann, H, et al.. (1977). [The effect of antifungal substances on the nitrogen distribution of dermatophytes. 8. Chemical and physiologic-chemical studies on dermatophytes].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 32(3). 186–186. 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.

Explore authors with similar magnitude of impact