Peter H. Heidemann

1.0k citations

18 papers · 607 indexed · h-index 12

Co-authors: Christian Körner Georg F. Hoffmann Eric G. Berger Verena Peters Christian Thiel Martin Hasilik Kurt Von Figura Stefan Höning
Topics: Lysosomal Storage Disorders Research (4 papers)Glycosylation and Glycoproteins Research (3 papers)Cellular transport and secretion (3 papers)
Cited by: Nephrology Genetics Molecular Biology
Journals: Journal of Clinical Investigation PLoS ONE The Journal of Clinical Endocrinology & Metabolism
Partner nations: Germany United States Switzerland

In The Last Decade

Peter H. Heidemann

18 papers receiving 585 citations

Peers

Countries citing papers authored by Peter H. Heidemann

Since Specialization

Citations

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

Fields of papers citing papers by Peter H. Heidemann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter H. Heidemann

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Sex chromosome DSD individuals with mosaic 45,X0 and aberrant Y chromosomes in 46,XY cells: distinct gender phenotypes and germ cell tumour risks^§ 2022 ·Systems Biology in Reproductive Medicine ·P. H. Vogt,(unknown),Markus Bettendorf,Petra Frank‐Herrmann,J. Zimmer,(unknown),(unknown),Daniela Choukair,Hans‐Peter Sinn,Helmuth-Guenther Doerr,Joachim Woelfle,Peter H. Heidemann,Yun‐Fai Chris Lau,Thomas Strowitzki	4
2	Clinical and Functional Characterization of a Patient Carrying a Compound Heterozygous Pericentrin Mutation and a Heterozygous IGF1 Receptor Mutation 2012 ·PLoS ONE ·(unknown),Désirée Dunstheimer,Jürgen Klammt,Daniela Friebe,Wieland Kieß,Jürgen Kratzsch,(unknown),Sandy Laue,Roland Pfäffle,(unknown),Peter H. Heidemann	15
3	Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey 2011 ·Clinical Endocrinology ·Friedhelm Raue,J. Pichl,(unknown),Dirk Schnabel,Peter H. Heidemann,G. Hammersen,Cornelia Jaursch-Hancke,Reinhard Santen,Christof Schöfl,Martin Wabitsch,Christine Haag,Egbert Schulze,Karin Frank‐Raue	64
4	Five novel mutations in steroidogenic factor 1 (SF1,NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency 2007 ·Human Mutation ·Birgit Köhler,Lin Lin,Bruno Ferraz‐de‐Souza,Peter Wieacker,Peter H. Heidemann,(unknown),Heike Biebermann,Dirk Schnabel,Annette Grüters,John C. Achermann	106
5	Insulin Tolerance Test Causes Hypokalaemia and Can Provoke Cardiac Arrhythmias 2004 ·Hormone Research in Paediatrics ·Gerhard Binder,(unknown),Matthias Gass,Michael B. Ranke,Peter H. Heidemann	28
6	Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation 2004 ·European Journal of Pediatrics ·Ute Hehr,Claudia Groß,(unknown),Dagmar Wahl,(unknown),Peter H. Heidemann,Andreas Hehr,(unknown)	40
7	Bi-allelic inactivation of the MEN1 tumor suppressor gene in human grade II astrocytoma☆ 2003 ·Cancer Letters ·Wölfram Karges,Beate Karges,Leopold Ludwig,Peter H. Heidemann	2
8	Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId 2002 ·Journal of Clinical Investigation ·(unknown),Christian Thiel,Torben Lübke,Martin Hasilik,Stefan Höning,Verena Peters,Peter H. Heidemann,Georg F. Hoffmann,Eric G. Berger,Kurt Von Figura,Christian Körner	76
9	Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId 2002 ·Journal of Clinical Investigation ·(unknown),Christian Thiel,Torben Lübke,Martin Hasilik,Stefan Höning,Verena Peters,Peter H. Heidemann,Georg F. Hoffmann,Eric G. Berger,Kurt Von Figura,Christian Körner	103
10	Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId 2002 ·Journal of Clinical Investigation ·(unknown),Christian Thiel,Torben Lübke,Martin Hasilik,Stefan Höning,Verena Peters,Peter H. Heidemann,Georg F. Hoffmann,Eric G. Berger,Kurt Von Figura,Christian Körner	11
11	Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease 2001 ·European Journal of Pediatrics ·(unknown),Thomas W. Apel,Peter H. Heidemann,Klaus Zerres,Hartmut P.H. Neumann,Helmuth G. Dörr	6
12	Functioning Thoracic Paraganglioma: Association with Von Hippel-Lindau Syndrome* 1997 ·The Journal of Clinical Endocrinology & Metabolism ·Bernhard U. Bender,(unknown),Andrzej Januszewicz,Roland Gärtner,Heinrich Schmidt,Michael M. Hoffmann,Peter H. Heidemann,Hartmut P.H. Neumann	16
13	Extracorporeal photochemotherapy as an effective treatment modality in chronic graft‐versus‐host disease 1996 ·Journal of the European Academy of Dermatology and Venereology ·B.-R. Balda,A. Konstantinow,Hans Starz,Astrid Gnekow,Peter H. Heidemann	14
14	A nonsense mutation in two German patients with fucosidosis 1995 ·Human Mutation ·Hee‐Chan Seo,Peter H. Heidemann,(unknown),John S. O’Brien	5
15	Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome) 1989 ·Human Genetics ·Susanne Schnittger,(unknown),Peter H. Heidemann,Friedrich Beermann,I. Hansmann	54
16	Influence of prenatal exposure to diethylstilbestrol on estrogen and progestin binding proteins in uteri and d1methylbenzanthracene‐induced mammary tumors of the rat 1981 ·Journal of Toxicology and Environmental Health ·Peter H. Heidemann,James L. Wittliff,Robert E. Calhoon,Elizabeth S. Boylan	4
17	Molecular heterogeneity of cytosolic forms of estrogen receptors from human breast tumors. 1978 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Timothy E. Kute,Peter H. Heidemann,(unknown)	47
18	Serum 3,5,3′-Triiodothyronine, Thyroxine, and Thyrotropin in Hypothyroid Infants with Congenital Goiter and the Response to Iodine 1978 ·The Journal of Clinical Endocrinology & Metabolism ·Peter H. Heidemann,P. Stubbe	12

About Peter H. Heidemann

Peter H. Heidemann is a scholar working on Genetics, Cell Biology and Endocrinology, Diabetes and Metabolism, having authored 18 papers that have together received 607 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Cellular transport and secretion (3 papers). The work is most often cited by research in Nephrology (60 citations), Genetics (234 citations) and Molecular Biology (360 citations). Peter H. Heidemann has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Christian Körner, Georg F. Hoffmann, Eric G. Berger, Verena Peters, Christian Thiel, Martin Hasilik, Kurt Von Figura, Stefan Höning, Torben Lübke and Timothy E. Kute. Their work appears in journals such as Journal of Clinical Investigation, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

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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