Wolfram Heinritz

1.2k total citations
28 papers, 380 citations indexed

About

Wolfram Heinritz is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Wolfram Heinritz has authored 28 papers receiving a total of 380 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Oncology. Recurrent topics in Wolfram Heinritz's work include Genomic variations and chromosomal abnormalities (4 papers), Corneal Surgery and Treatments (3 papers) and DNA Repair Mechanisms (2 papers). Wolfram Heinritz is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Corneal Surgery and Treatments (3 papers) and DNA Repair Mechanisms (2 papers). Wolfram Heinritz collaborates with scholars based in Germany, United States and Poland. Wolfram Heinritz's co-authors include Ursula G. Froster, G. Duncker, Canan Uçar, Christiane Zweier, Denise Horn, Henrik Köhler, Zsófia Nemoda, Anita Rauch, H.‐J. Glander and Steffen Syrbe and has published in prestigious journals such as International Journal of Cancer, British Journal of Dermatology and British Journal of Ophthalmology.

In The Last Decade

Wolfram Heinritz

27 papers receiving 359 citations

Peers

Countries citing papers authored by Wolfram Heinritz

Since Specialization

Citations

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

Fields of papers citing papers by Wolfram Heinritz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wolfram Heinritz

This figure shows the co-authorship network connecting the top 25 collaborators of Wolfram Heinritz. A scholar is included among the top collaborators of Wolfram Heinritz 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 Wolfram Heinritz. Wolfram Heinritz 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	Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome 2014 ·BMC Medical Genetics ·Wenke Seifert, Peter Meinecke, Gabriele Krüger, Eva Rossier, Wolfram Heinritz, (unknown), Denise Horn	23
2	Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome 2013 ·European Journal of Human Genetics ·Denise Horn, Dagmar Wieczorek, Kay Metcalfe, Ivo Barić, (unknown), Mario Ćuk, Danijela Petković Ramadža, Ulrike Krüger, Stephanie Demuth, Wolfram Heinritz, Tobias Linden, Jens Koenig, Peter N. Robinson, Peter Krawitz	31
3	Association of death receptor 4 variant (683A>C) with ovarian cancer risk in BRCA1 mutation carriers 2011 ·International Journal of Cancer ·(unknown), Beatrix Versmold, Christoph Engel, Alfons Meindl, Norbert Arnold, (unknown), Christian Sutter, Dieter Niederacher, Helmut Deißler, Sabine Preisler‐Adams, Karin Kast, Dieter Schäfer, Dorothea Gadzicki, Wolfram Heinritz, Barbara Wappenschmidt, Rita K. Schmutzler	8
4	Evaluation of IP-RP-HPLC for Length Determination of the Trinucleotide Repeat Fragments in Huntington's Disease 2010 ·Journal of Chromatographic Science ·Marzena Skrzypczak-Zielińska, Wolfram Heinritz, Anja Schulz, Marek Mierzejewski, Ursula G. Froster	0
5	Multiple trichoepitheliomas – a novel mutation in the CYLD gene 2009 ·Journal of the European Academy of Dermatology and Venereology ·(unknown), Isabel Cristina Martins de Freitas, (unknown), Ana Afonso, Marzena Skrzypczak-Zielińska, Wolfram Heinritz	11
6	New Mutations of EXT1 and EXT2 Genes in German Patients with Multiple Osteochondromas 2009 ·Annals of Human Genetics ·Wolfram Heinritz, Ulrike Hüffmeier, (unknown), Bianca Miterski, Christiane Zweier, (unknown), Axel Bohring, Beate Mitulla, (unknown), Ursula G. Froster	24
7	Macular corneal dystrophy: mutational spectrum in German patients, novel mutations and therapeutic options 2008 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·(unknown), (unknown), Wolfram Heinritz, Ursula G. Froster, G. Duncker	34
8	TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings 2008 ·British Journal of Ophthalmology ·(unknown), (unknown), E. Weidle, (unknown), Frank Tost, H. E. Völcker, Dirk Schulze, Wolfram Heinritz, Thomas Reinhard, (unknown), G. Duncker, Daniel F. Schorderet, Claudia Auw‐Haedrich	18
9	Functional analysis of the novel TBX5c.1333delC mutation resulting in an extended TBX5 protein 2008 ·BMC Medical Genetics ·Johann Böhm, Wolfram Heinritz, (unknown), Mihailo Vujic, Britt‐Marie Ekman‐Joelsson, Jürgen Kohlhase, Ursula G. Froster	17
10	Evidence for a Founder Effect of the Germline Fumarate Hydratase Gene Mutation R58P causing Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) 2007 ·Annals of Human Genetics ·Wolfram Heinritz, Uwe Paasch, Michael Sticherling, Ch. Wittekind, (unknown), (unknown), Regina Renner	11
11	A missense mutation in the ZFHX1B gene associated with an atypical Mowat–Wilson syndrome phenotype 2006 ·American Journal of Medical Genetics Part A ·Wolfram Heinritz, Christiane Zweier, Ursula G. Froster, (unknown), (unknown), Steffen Syrbe, Anita Rauch, Volker Schuster	28
12	MYH Gene Status in Polish FAP Patients without APC Gene Mutations 2006 ·Hereditary Cancer in Clinical Practice ·Marzena Skrzypczak-Zielińska, (unknown), Wolfram Heinritz, Ursula G. Froster, Daniel Lipiński, Ryszard Słomski, Andrzej Pławski	2
13	A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene 2006 ·British Journal of Dermatology ·Wolfram Heinritz, Sonja Grunewald, (unknown), (unknown), Ursula G. Froster, H.‐J. Glander, Uwe Paasch, Jan C. Simon	15
14	Gene conversion cetween functional trypsinogen genesPRSS1andPRSS2associated with chronic pancreatitis in a six-year-old girl 2005 ·Human Mutation ·Niels Teich, Zsófia Nemoda, Henrik Köhler, Wolfram Heinritz, Joachim Mössner, Volker Keim, Miklós Sahin‐Tóth	30
15	Hereditäre multiple Exostosen 2005 ·Der Orthopäde ·Wolfram Heinritz, (unknown), (unknown), Peter Matzen, Ursula G. Froster	2
16	The human TBX5 gene mutation database 2005 ·Human Mutation ·Wolfram Heinritz, (unknown), (unknown), Ursula G. Froster	30
17	Pre-eclampsia as a ‘Three Stage Problem’—A Workshop Report 2004 ·Placenta ·Holger Stepan, R Faber, (unknown), Wolfram Heinritz, Henri Wallaschofski, Ralf Dechend, Thomas Walther, Berthold Huppertz	4
18	Another case of autosomal dominant exstrophy of the bladder 2004 ·Prenatal Diagnosis ·Ursula G. Froster, Wolfram Heinritz, J Bennek, L.-C. Horn, R Faber	7
19	Molecular and cytogenetic characterization of a non‐mosaic isodicentric Y chromosome in a patient with Klinefelter syndrome 2004 ·American Journal of Medical Genetics Part A ·Wolfram Heinritz, Dieter Kotzot, Stefan Heinze, (unknown), Werner Johann Kleemann, Ursula G. Froster	7
20	Molekulargenetischer Mutationsnachweis im PTPN11-Gen beim Multiple-Lentigines- (LEOPARD-)Syndrom 2003 ·Der Hautarzt ·(unknown), H.‐J. Glander, Wolfram Heinritz	5

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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