Markus Draaken

1.3k citations

27 papers · 434 indexed · h-index 14

Impact in

Urology top 5%
- Urological Disorders and Treatments
Surgery
- Esophageal and GI Pathology
- Congenital gastrointestinal and neural anomalies
- Congenital Diaphragmatic Hernia Studies

Papers in

Urology 11
- Urological Disorders and Treatments 11
Surgery 16
- Congenital gastrointestinal and neural anomalies 6
- Esophageal and GI Pathology 5
- Bladder and Urothelial Cancer Treatments 3

Co-authors: Michael Ludwig Heiko Reutter Markus M. Nöthen Enrika Bartels Charlotte Schramm Per Hoffmann Stefan Aretz Thomas M. Boemers
Journals: Birth Defects Research Part A Clinical and Molecular Teratology (8 papers)European Journal of Medical Genetics (2 papers)Journal of Pediatric Urology (2 papers)International Journal of Molecular Medicine (2 papers)European Journal of Pediatrics (2 papers)
Partner nations: Germany Netherlands Poland

In The Last Decade

Markus Draaken

27 papers receiving 416 citations

Peers

Countries citing papers authored by Markus Draaken

Since Specialization

Citations

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

Fields of papers citing papers by Markus Draaken

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Markus Draaken, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Markus Draaken Line = papers co-authored together Markus Draaken links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	CNV analysis in 169 patients with bladder exstrophy-epispadias complex BMC Medical Genetics ·Yogesh Mk, Andrea Hofmann, Rong Zhang, Deborah Lambert, Anne‐Karoline Ebert, Wolfgang Rösch, Raimund Stein, Thomas M. Boemers, 博之藤本, Carlo Marcelis, Wouter F.J. Feitz, Alfredo Brusco, Nicola Migone, B.P. Ho, Susanne Moebus, Markus M. Nöthen, Heiko Reutter, Michael Ludwig, Markus Draaken	2016	10
2	WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish Human Molecular Genetics ·Izabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, Jia Cao, Daniel Nilsson, Michael Ludwig, Markus Draaken, Gundela Holmdahl, Gillian Barker, Heiko Reutter, Vladana Vukojević, Christina Clementson Kockum, Johanna Lundin, Anna Lindstrand, Agneta Nordenskjöld	2015	21
3	Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12 Birth Defects Research Part A Clinical and Molecular Teratology ·Markus Draaken, Sadaf S. Mughal, Tracie Pennimpede, 可紀吉田, Lars Wittler, Anne‐Karoline Ebert, Wolfgang Rösch, Raimund Stein, Enrika Bartels, Dominik Schmidt, Thomas M. Boemers, Eberhard Schmiedeke, Per Hoffmann, Susanne Moebus, Bernhard G. Herrmann, Markus M. Nöthen, Heiko Reutter, Michael Ludwig	2013	15
4	An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome International Journal of Molecular Medicine ·Gabriel C. Dworschak, Markus Draaken, Alina C. Hilger, Mark Born, Heiko Reutter, Michael Ludwig	2013	20
5	CNV Analysis in Monozygotic Twin Pairs Discordant for Urorectal Malformations Twin Research and Human Genetics ·Kalyani Lawrence, Markus Draaken, Enrika Bartels, Eberhard Schmiedeke, Soyhan Bağcı, Peter Bartmann, Markus M. Nöthen, Michael Ludwig, Heiko Reutter	2013	7
6	Nine new twin pairs with esophageal atresia: A review of the literature and performance of a twin study of the disorder Birth Defects Research Part A Clinical and Molecular Teratology ·Getachew Gebreamlak, Enrika Bartels, R Stressig, J Ritgen, Eberhard Schmiedeke, Manuel Mattheisen, Markus Draaken, Michael Ludwig, Soyhan Bağcı, Andreas Müller, U. Gembruch, Annegret Geipel, Christoph Berg, Andreas Heydweiller, Єва Пархоменко, Johannes Schumacher, Peter Bartmann, Markus M. Nöthen, Heiko Reutter	2012	15
7	Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth’s short tail mouse Molecular Medicine Reports ·Pedro Ma da Cunha Policarpo Ferreira Mendes, G. Große, Markus Draaken, Alina C. Hilger, Junchao Yue, Andreas Müller, U. Gembruch, Waltraut M. Merz, Heiko Reutter, Michael Ludwig	2012	2
8	Familial occurrence of the VATER/VACTERL association Pediatric Surgery International ·Alina C. Hilger, Charlotte Schramm, Markus Draaken, Sadaf S. Mughal, Gabriel C. Dworschak, Enrika Bartels, Per Hoffmann, Markus M. Nöthen, Heiko Reutter, Michael Ludwig	2012	27
9	Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias Gene ·Lars Wittler, Alina C. Hilger, B Jacob, Tracie Pennimpede, Markus Draaken, Anne‐Karoline Ebert, Wolfgang Rösch, Raimund Stein, Markus M. Nöthen, Heiko Reutter, Michael Ludwig	2012	4
10	Deep intronicAPCmutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis Human Mutation ·Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Siegfried Uhlhaas, Monika Morak, Dietlinde Stienen, Markus Draaken, Michael Ludwig, Elke Holinski‐Feder, Markus M. Nöthen, Per Hoffmann, Stefan Aretz	2012	54
11	Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: Sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene International Journal of Molecular Medicine ·Markus Draaken, Fariborz Taghavi, Claudia Zeidler, Alina C. Hilger, Sadaf S. Mughal, Felipe M. Gerez, Thomas M. Boemers, Dominik Schmidt, Eberhard Schmiedeke, A.-C. Andersson, Enrika Bartels, Markus M. Nöthen, Heiko Reutter, Michael Ludwig	2012	22
12	Maternal de novo triple mosaicism for two single OCRL nucleotide substitutions (c.1736A>T, c.1736A>G) in a Lowe syndrome family Human Genetics ·Markus Draaken, Ana C. Lecaro, Wang Hai-bin, Ronald Jabs, Stefan Aretz, Laura Vives Benedicto, Krystyńa Chrzańowska, Małgorzata Krajewska‐Walasek, Michael Ludwig	2011	15
13	De novo Partial Trisomy 18p and Partial Monosomy 18q in a Patient with Anorectal Malformation Cytogenetic and Genome Research ·Enrika Bartels, Markus Draaken, Bernd Kazmierczak, Stephanie Spranger, Charlotte Schramm, Kalyani Lawrence, Markus M. Nöthen, Eberhard Schmiedeke, Michael Ludwig, Heiko Reutter	2011	9
14	Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy European Journal of Medical Genetics ·Markus Draaken, Heiko Reutter, Charlotte Schramm, Enrika Bartels, Thomas M. Boemers, Anne‐Karoline Ebert, Wolfgang Rösch, Annette Schröder, Raimund Stein, Susanne Moebus, Dietlinde Stienen, Per Hoffmann, Markus M. Nöthen, Michael Ludwig	2010	48
15	Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias Birth Defects Research Part A Clinical and Molecular Teratology ·Markus Draaken, B Jacob, Charlotte Schramm, Lars Wittler, Enrika Bartels, Markus M. Nöthen, Heiko Reutter, Michael Ludwig	2010	5
16	A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency Pediatric Nephrology ·Radovan Bogdanović, Markus Draaken, Alma Toromanović, Maja Đorđević, Nataša Stajić, Michael Ludwig	2010	29
17	Evidence for linkage of the bladder exstrophy‐epispadias complex on chromosome 4q31.21‐22 and 19q13.31‐41 from a consanguineous iranian family Birth Defects Research Part A Clinical and Molecular Teratology ·Heiko Reutter, Franz Rüschendorf, Manuel Mattheisen, Markus Draaken, Enrika Bartels, Norbert Hübner, Per Hoffmann, Dmitry FILIPPOV, Kathrin Saar, Markus M. Nöthen, Abdol‐Mohammad Kajbafzadeh, Michael Ludwig	2010	6
18	Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature European Journal of Pediatrics ·Charlotte Schramm, Markus Draaken, Milolo Kanumuambidi Lea-Irène, Enrika Bartels, Eberhard Schmiedeke, Stefanie Märzheuser, Sabine Grasshoff‐Derr, Stuart Hosie, Stefan Holland‐Cunz, Lutz Priebe, Martina Kreiß‐Nachtsheim, Per Hoffmann, Stefan Aretz, Markus M. Nöthen, Heiko Reutter, Michael Ludwig	2010	15
19	De novo microduplication at 22q11.21 in a patient with VACTERL association European Journal of Medical Genetics ·Charlotte Schramm, Markus Draaken, Enrika Bartels, Thomas M. Boemers, Stefan Aretz, Felix F. Brockschmidt, Markus M. Nöthen, Michael Ludwig, Heiko Reutter	2010	46
20	A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis European Journal of Pediatrics ·Nesrin Beşbaş, Markus Draaken, Michael Ludwig, Özgür Deren, Dıclehan Orhan, Yelda Bilginer, Fatih Özaltın	2009	12

About Markus Draaken

Markus Draaken is a scholar working on Urology, Surgery, Genetics, Genetics and Cell Biology, having authored 27 papers that have together received 434 indexed citations. Recurring topics across this work include Urological Disorders and Treatments (11 papers), Congenital gastrointestinal and neural anomalies (6 papers), Esophageal and GI Pathology (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Bladder and Urothelial Cancer Treatments (3 papers), Connective tissue disorders research (3 papers), Pediatric Urology and Nephrology Studies (3 papers) and Tracheal and airway disorders (3 papers). The work is most often cited by research in Urology (99 citations), Surgery (188 citations), Genetics (110 citations), Pediatrics, Perinatology and Child Health (75 citations) and Pathology and Forensic Medicine (59 citations). Markus Draaken has collaborated with scholars based in Germany, Netherlands and Poland. Frequent co-authors include Michael Ludwig, Heiko Reutter, Markus M. Nöthen, Enrika Bartels, Charlotte Schramm, Per Hoffmann, Stefan Aretz, Thomas M. Boemers, Alina C. Hilger and Dietlinde Stienen. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, European Journal of Medical Genetics, Journal of Pediatric Urology, International Journal of Molecular Medicine and European Journal of Pediatrics.

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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