K. Bartholomé

1.3k total citations
27 papers, 931 citations indexed

About

K. Bartholomé is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, K. Bartholomé has authored 27 papers receiving a total of 931 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Clinical Biochemistry, 14 papers in Molecular Biology and 8 papers in Physiology. Recurrent topics in K. Bartholomé's work include Metabolism and Genetic Disorders (20 papers), Metabolomics and Mass Spectrometry Studies (6 papers) and Diet and metabolism studies (6 papers). K. Bartholomé is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Metabolomics and Mass Spectrometry Studies (6 papers) and Diet and metabolism studies (6 papers). K. Bartholomé collaborates with scholars based in Germany, United States and Poland. K. Bartholomé's co-authors include Peter Lutz, Horst Bickel, Seymour Kaufman, D. J. Byrd, Jacques Mallet, P.M. Knappskog, Torgeir Flatmark, Sheldon Milstien, C. Aulehla‐Scholz and Bernd Dworniczak and has published in prestigious journals such as The Lancet, PEDIATRICS and Journal of Allergy and Clinical Immunology.

In The Last Decade

K. Bartholomé

27 papers receiving 852 citations

Peers

Countries citing papers authored by K. Bartholomé

Since Specialization

Citations

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

Fields of papers citing papers by K. Bartholomé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Bartholomé

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Mutations in the Tyrosine Hydroxylase Gene Cause Various Forms of L-Dopa-Responsive Dystonia 1997 ·Advances in pharmacology ·K. Bartholomé, (unknown)	12
2	Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene 1995 ·Human Molecular Genetics ·P.M. Knappskog, Torgeir Flatmark, Jacques Mallet, (unknown), K. Bartholomé	157
3	Ring chromosome 22: A case report* 1991 ·Klinische Pädiatrie ·(unknown), Stephan B. Felix, K. Bartholomé	3
4	Phenylalanine hydroxylase gene: Novel missense mutation in exon 7 causing severe phenylketonuria 1991 ·Genomics ·Bernd Dworniczak, (unknown), (unknown), K. Bartholomé, C. Aulehla‐Scholz, Jürgen Horst	40
5	Aberrant splicing of phenylalanine hydroxylase mRNA: The major cause for phenylketonuria in parts of southern Europe 1991 ·Genomics ·Bernd Dworniczak, C. Aulehla‐Scholz, Luba Kalaydjieva, K. Bartholomé, (unknown), J. Horst	68
6	Biochemical and Neurophysiological Investigations in Two Forms of Segawa's Disease 1990 ·Neuropediatrics ·(unknown), K. Bartholomé	10
7	PRENATAL DIAGNOSIS IN CYSTIC FIBROSIS 1985 ·The Lancet ·(unknown), L. Mathy, K.-H. Grzeschik, A.J. Driesel, K. Bartholomé, Michael Neugebauer, K. Olek	4
8	[Nontraumatic rhabdomyolysis with reversible acute kidney failure following hyperosmolar diabetic coma in a child]. 1984 ·PubMed ·(unknown), N Graben, (unknown), E. Kreuzfelder, K. Bartholomé	2
9	[Anaphylactic reactions in mediastinal echinococcosis]. 1983 ·PubMed ·(unknown), (unknown), K. Bartholomé, U. Wahn	2
10	DEFICIENCY OF TYROSINE HYDROXYLASE OR TRYPTOPHAN HYDROXYLASE: A POSSIBLE CAUSE OF TWO HYPOTHETICAL METABOLIC DISEASES 1983 ·Acta Paediatrica ·K. Bartholomé	5
11	In Vivo residual activities of the phenylalanine hydroxylating system in phenylketonuria and variants 1981 ·Journal of Inherited Metabolic Disease ·Friedrich K. Trefz, K. Bartholomé, Horst Bickel, Peter Lutz, Heinrich Schmidt, (unknown)	23
12	Nitrogen metabolism and growth in experimental uremia. 1980 ·PubMed ·Otto Mehls, E Ritz, G Gilli, K. Bartholomé, (unknown), M. Hohenegger, (unknown)	13
13	Tetrahydrobiopterin therapy of atypical phenylketonuria due to defective dihydrobiopterin biosynthesis. 1978 ·Archives of Disease in Childhood ·(unknown), (unknown), H.‐Ch. Curtius, A. Niederwieser, K. Bartholomé, M. Viscontini, (unknown), Jost H. Bieri	43
14	IMMUNOLOGICAL DETECTION OF PHENYLALANINE HYDROXYLASE IN PHENYLKETONURIA 1978 ·The Lancet ·K. Bartholomé, (unknown)	3
15	Malignant hyperphenylalaninaemia—Current status (June 1977) 1978 ·Journal of Inherited Metabolic Disease ·D. M. Danks, K. Bartholomé, B. E. Clayton, H.‐Ch. Curtius, H Gröbe, Seymour Kaufman, R.J. Leeming, W. PFLEIDERER, Heinz Rembold, F.A. Rey	78
16	L-DOPA AND 5-HYDROXYTRYPTOPHAN THERAPY IN PHENYLKETONURIA WITH NORMAL PHENYLALANINE-HYDROXYLASE ACTIVITY 1975 ·The Lancet ·K. Bartholomé, D. J. Byrd	39
17	Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and Hyperphenylalaninemia 1975 ·Pediatric Research ·K. Bartholomé, Peter Lutz, Horst Bickel	80
18	Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and Hyperphenylalaninemia 1975 ·Pediatric Research ·K. Bartholomé, Peter Lutz, Horst Bickel	20
19	A NEW MOLECULAR DEFECT IN PHENYLKETONURIA 1974 ·The Lancet ·K. Bartholomé	70
20	Purification and Properties of Extra- and Intramitochondrial Malate Dehydrogenase (NADP; Decarboxylating) From Pig Heart 1972 ·Hoppe-Seyler´s Zeitschrift für physiologische Chemie ·K. Bartholomé, Dieter Brdiczka, Dirk Pette	39

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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