Christian Kranz

1.2k citations

21 papers · 956 indexed · h-index 17

Co-authors: Hudson H. Freeze Jonas Denecke Thorsten Marquardt Liangwu Sun Erik Harms Erik A. Eklund Vladimir Lupashin Thomas Brune
Topics: Glycosylation and Glycoproteins Research (19 papers)Carbohydrate Chemistry and Synthesis (16 papers)Galectins and Cancer Biology (6 papers)
Cited by: Cell Biology Molecular Biology Immunology
Journals: Journal of Clinical Investigation Molecular and Cellular Biology The American Journal of Human Genetics
Partner nations: United States Germany Netherlands

In The Last Decade

Christian Kranz

21 papers receiving 932 citations

Peers

Countries citing papers authored by Christian Kranz

Since Specialization

Citations

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

Fields of papers citing papers by Christian Kranz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Kranz

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Kranz. A scholar is included among the top collaborators of Christian Kranz 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 Christian Kranz. Christian Kranz 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	Endoglycosidase and Glycoamidase Release of N‐Linked Glycans 2010 ·Current Protocols in Protein Science ·Hudson H. Freeze,Christian Kranz	84
2	Endoglycosidase and Glycoamidase Release of N‐Linked Glycans 2010 ·Current Protocols in Molecular Biology ·Hudson H. Freeze,Christian Kranz	51
3	Endoglycosidase and Glycoamidase Release of N‐Linked Glycans 2010 ·Current Protocols in Immunology ·Hudson H. Freeze,Christian Kranz	27
4	Hypoglycosylation due to dolichol metabolism defects 2009 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jonas Denecke,Christian Kranz	29
5	Endoglycosidase and Glycoamidase Release of N‐Linked Glycans 2008 ·Current Protocols in Immunology ·Hudson H. Freeze,Christian Kranz	11
6	A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy 2007 ·The American Journal of Human Genetics ·Christian Kranz,(unknown),Jonas Denecke,(unknown),(unknown),Volker Debus,Hans-Gerd Kehl,Erik Harms,A. D. Reith,(unknown),H Gröbe,G. Hammersen,(unknown),Thorsten Marquardt	72
7	Expanding spectrum of congenital disorder of glycosylation Ig (CDG‐Ig): Sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality 2007 ·American Journal of Medical Genetics Part A ·Christian Kranz,Alice Basinger,Müge Güçsavaş‐Çalıkoğlu,Liangwu Sun,Cynthia M. Powell,Frederick W. Henderson,Arthur S. Aylsworth,Hudson H. Freeze	65
8	Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS) 2007 ·Glycoconjugate Journal ·Jonas Denecke,Christian Kranz,Manfred Nimtz,Harald S. Conradt,Thomas Brune,H. Heimpel,Thorsten Marquardt	17
9	CDG‐Id in two siblings with partially different phenotypes 2007 ·American Journal of Medical Genetics Part A ·Christian Kranz,Liangwu Sun,Erik A. Eklund,Donna M. Krasnewich,Janet R. Casey,Hudson H. Freeze	31
10	Molecular and clinical characterization of a Moroccan Cog7 deficient patient 2007 ·Molecular Genetics and Metabolism ·Bobby G. Ng,Christian Kranz,Eveline Hagebeuk,M. Durán,N. G. G. M. Abeling,Birgitte Wuyts,Dániel Ungár,Vladimir Lupashin,(unknown),Bwee Tien Poll‐The,Hudson H. Freeze	46
11	COG8 deficiency causes new congenital disorder of glycosylation type IIh 2007 ·Human Molecular Genetics ·Christian Kranz,Bobby G. Ng,Liangwu Sun,Vandana Sharma,Erik A. Eklund,Yoshiaki Miura,Dániel Ungár,Vladimir Lupashin,(unknown),John F. Cipollo,Catherine E. Costello,Eva Loh,Wanjin Hong,Hudson H. Freeze	95
12	A homozygousZMPSTE24null mutation in combination with a heterozygous mutation in theLMNAgene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS 2006 ·Human Mutation ·Jonas Denecke,Thomas Brune,(unknown),Horst Robenek,Christian Kranz,Richard J. Auchus,Anil K. Agarwal,Thorsten Marquardt	66
13	Endoglycosidase and Glycoamidase Release of N‐Linked Oligosaccharides 2006 ·Current Protocols in Protein Science ·Hudson H. Freeze,Christian Kranz	9
14	Congenital Disorder of Glycosylation Type Id: Clinical Phenotype, Molecular Analysis, Prenatal Diagnosis, and Glycosylation of Fetal Proteins 2005 ·Pediatric Research ·Jonas Denecke,Christian Kranz,(unknown),Kristin Bosse,Peter Herkenrath,Otfried Debus,Erik Harms,Thorsten Marquardt	40
15	An activated 5? cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id) 2004 ·Human Mutation ·Jonas Denecke,Christian Kranz,Dirk Kemming,Hans-Georg Koch,Thorsten Marquardt	48
16	Congenital Disorder of Glycosylation Type Ik (CDG-Ik): A Defect of Mannosyltransferase I 2004 ·The American Journal of Human Genetics ·Christian Kranz,Jonas Denecke,Ludwig Lehle,Kristina Sohlbach,(unknown),Friedhelm Meinhardt,Rainer Rossi,Sonja Gudowius,Thorsten Marquardt	62
17	cycloSaligenyl‐mannose‐1‐monophosphates as a New Strategy in CDG‐Ia Therapy: Hydrolysis, Mechanistic Insights and Biological Activity 2004 ·European Journal of Organic Chemistry ·(unknown),Christian Kranz,Thorsten Marquardt,Chris Meier	16
18	Membrane-Permeant derivatives of mannose-1-phosphate 2002 ·Bioorganic & Medicinal Chemistry ·(unknown),Joachim Thiem,Christian Kranz,Thorsten Marquardt	26
19	A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If) 2001 ·Journal of Clinical Investigation ·Christian Kranz,Jonas Denecke,Mark A. Lehrman,Sutapa Ray,(unknown),(unknown),Dijana Šagi,Jasna Peter‐Katalinić,Hudson H. Freeze,Thomas Schmid,(unknown),Erik Harms,Thorsten Marquardt	104
20	A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If) 2001 ·Journal of Clinical Investigation ·Christian Kranz,Jonas Denecke,Mark A. Lehrman,Sutapa Ray,(unknown),(unknown),Dijana Šagi,Jasna Peter‐Katalinić,Hudson H. Freeze,Thomas Schmid,(unknown),Erik Harms,Thorsten Marquardt	7

About Christian Kranz

Christian Kranz is a scholar working on Organic Chemistry, Cell Biology and Molecular Biology, having authored 21 papers that have together received 956 indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (19 papers), Carbohydrate Chemistry and Synthesis (16 papers) and Galectins and Cancer Biology (6 papers). The work is most often cited by research in Cell Biology (204 citations), Molecular Biology (784 citations) and Immunology (211 citations). Christian Kranz has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Hudson H. Freeze, Jonas Denecke, Thorsten Marquardt, Liangwu Sun, Erik Harms, Erik A. Eklund, Vladimir Lupashin, Thomas Brune, Dániel Ungár and Bobby G. Ng. Their work appears in journals such as Journal of Clinical Investigation, Molecular and Cellular Biology and The American Journal of Human Genetics.

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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