Timm O. Goecke

2.9k citations

33 papers · 1.2k indexed · h-index 20

Developmental Biology top 5%
- Congenital limb and hand anomalies 7
Pathology and Forensic Medicine top 5%
- Genetic factors in colorectal cancer 6
Genetics top 5%
- Connective tissue disorders research 6
- Genomic variations and chromosomal abnormalities 5
- BRCA gene mutations in cancer 3
Cancer Research top 10%
- Cancer Genomics and Diagnostics 4
Rheumatology top 10%
Molecular Biology
- Hedgehog Signaling Pathway Studies 3
Plant Science
- Chromosomal and Genetic Variations 3

Co-authors: F. Majewski John M. Opitz Christoph Engel Gabriela Möslein Karsten Schulmann Frank Majewski Wolfgang Küster Matthias Kloor
Cited by: Developmental Biology Pathology and Forensic Medicine Genetics
Journals: Human Genetics (2 papers)European Journal of Pediatrics (2 papers)European Journal of Human Genetics (1 paper)
Partner nations: Germany United States Türkiye

In The Last Decade

Timm O. Goecke

32 papers receiving 1.2k citations

Peers

Countries citing papers authored by Timm O. Goecke

Since Specialization

Citations

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

Fields of papers citing papers by Timm O. Goecke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Timm O. Goecke. 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 Timm O. Goecke. The network helps show where Timm O. Goecke may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Timm O. Goecke, 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 Timm O. Goecke Line = papers co-authored together Timm O. Goecke links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9 American Journal of Medical Genetics Part A ·Johanna Christina Czeschik,R. Gallardo,Timm O. Goecke,Hermann‐Josef Lüdecke,Nicholas Wagner,Alma Kuechler,Dagmar Wieczorek	2013	24
2	Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management Breast Cancer Research and Treatment ·Simone Heidemann,Christine Fischer,Christoph Engel,Barbara Fischer,Lana Harder,Brigitte Schlegelberger,Dieter Niederacher,Timm O. Goecke,Sandra C. Doelken,Nicola Dikow,W. Jonat,Susanne Morlot,LaurenceFriendPellTemple J. A.A. L.E. J.P. J.,Norbert Arnold	2012	43
3	Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies Familial Cancer ·Karin Hardt,馨子梶山,Beate Betz,Timm O. Goecke,苏冠龙,D. Hoyland,Kati Servan,Verena Steinke,Nils Rahner,Monika Morak,Elke Holinski‐Feder,Christoph Engel,Gabriela Möslein,大宮喜文,Magnus von Knebel Doeberitz,Christian Pox,Johannes H. Hegemann,Brigitte Royer‐Pokora	2011	22
4	Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers International Journal of Colorectal Disease ·Janesandre Palilingan,Anke Reinacher‐Schick,Karsten Schulmann,Christian Pox,Jörg Willert,Andrea Tannapfel,Stefan Heringlake,Timm O. Goecke,Stefan Aretz,Susanne Stemmler,Wolff Schmiegel	2009	38
5	Efficacy of Annual Colonoscopic Surveillance in Individuals With Hereditary Nonpolyposis Colorectal Cancer Clinical Gastroenterology and Hepatology ·Christoph Engel,Nils Rahner,Karsten Schulmann,Elke Holinski‐Feder,Timm O. Goecke,Hans K. Schackert,Matthias Kloor,Verena Steinke,H. Vogelsang,Gabriela Möslein,Heike Görgens,Nancy Judith Genes Roqueme,Magnus von Knebel Doeberitz,Josef Rüschoff,Nicolaus Friedrichs,Reinhard Büttner,Markus Loeffler,Peter Propping,Wolff Schmiegel	2009	107
6	Congenital central hypoventilation syndrome with hyperinsulinism in a preterm infant Journal of Human Genetics ·Ulrike Hennewig,Amini Shohreh,Markus Vogel,Thomas Meißner,Timm O. Goecke,Hartmut Peters,Leslie Veen,Ertan Mayatepek,Thomas Hoehn	2008	33
7	MLPA screening in theBRCA1gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases Human Mutation ·Stefanie Engert,Barbara Wappenschmidt,Beate Betz,Karin Kast,Michael Kutsche,Heide Hellebrand,Timm O. Goecke,Marion Kiechle,Dieter Niederacher,Rita K. Schmutzler,Alfons Meindl	2008	74
8	A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN The American Journal of Human Genetics ·Katarina Lehmann,Petra Seemann,Fatma Sılan,Timm O. Goecke,奈啓朝比,Klaus Kjaer,Søren K. Kjærgaard,M J Mahoney,Susanne Morlot,Carsten Reißner,Bronwyn Kerr,Andrew O.M. Wilkie,Stefan Mundlos	2007	84
9	Gene expression in acute Stanford type A dissection: a comparative microarray study Journal of Translational Medicine ·Barbara Weis-Müller,Olga Modlich,Stefania Izzo,Yanwen E. Liu,Rita Huber,Hans Bojar,Jochen D. Schipke,P. Feindt,E. Gams,Wolfram Müller,Timm O. Goecke,W. Sandmann	2006	47
10	Age of uptake of early cancer detection facilities by low-risk and high-risk patients with familial breast and ovarian cancer European Journal of Cancer Prevention ·Michael P. Lux,Sven Ackermann,Mayada R. Bani,高光锋,Timm O. Goecke,Dieter Niederacher,Ribeiro Marcelo,Etienne de Vaumas,Isabela Lemos Veloso Lopes,Peter A. Fasching	2005	10
11	Spectrum and frequencies of mutations inMSH2 andMLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer International Journal of Cancer ·Elisabeth Mangold,Constanze Pagenstecher,Waltraut Friedl,Micaela Mathiak,Reinhard Buettner,Christoph Engel,Markus Loeffler,Elke Holinski‐Feder,С.С. Абрамчук,Gisela Keller,Hans K. Schackert,Stefan Krüger,Timm O. Goecke,Gabriela Möslein,Matthias Kloor,Johannes Gebert,Erdmute Kunstmann,Karsten Schulmann,Josef Rüschoff,Peter Propping	2005	95
12	Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects European Journal of Human Genetics ·Wim Wuyts,Gérard Waeber,Peter Meinecke,Herdit M. Schüler,Timm O. Goecke,Wim Van Hul,Oliver Bartsch	2004	13
13	Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1 American Journal of Medical Genetics Part A ·Georg C. Schwabe,Seval Türkmen,Gundula Leschik,Şükrü Palanduz,B. Stöver,Timm O. Goecke,Stefan Mundlos	2003	51
14	Gene Expression Profiles in the Acutely Dissected Human Aorta European Journal of Vascular and Endovascular Surgery ·Bárbara Müller,Olga Modlich,Hyung Bum An,Hans Bojar,Jochen D. Schipke,Timm O. Goecke,P. Feindt,Thomas Petzold,E. Gams,Wolfram Müller,W. Hort,W. Sandmann	2002	47
15	Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium Cytogenetic and Genome Research ·Kerstin Kutsche,James M. McKearin,Sascha Knauf,DeWayne Arrington,Martina Schmidt,Bernd Schröder,Hans Gerd Nothwang,H. Schüler,Timm O. Goecke,Petra Du Toit,Christian L. Althaus,Andreas Gal	2000	7
16	Microcephalic osteodysplastic primordial dwarfism type ii: Report of three cases and review American Journal of Medical Genetics ·Frank Majewski,Timm O. Goecke	1998	29
17	Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family Movement Disorders ·Barbara Leube,Kirn R. Kessler,Timm O. Goecke,Georg Auburger,R. Benecke	1997	63
18	Progressive erythrokeratodermia and cochlear hearing impairment. A case report and review of the literature International Journal of Pediatric Otorhinolaryngology ·陈保林,Timm O. Goecke,I. Anton‐Lamprecht,Wolfgang Küster	1988	10
19	Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome? Human Genetics ·F. Majewski,Yifei Ren,Timm O. Goecke,H. Kemperdick	1983	14
20	Metabolic Research in MZ Twins with Diabetes Mellitus. Progress Report Acta geneticae medicae et gemellologiae ·Timm O. Goecke,Ali Mutahar	1974	2

About Timm O. Goecke

Timm O. Goecke is a scholar working on Developmental Biology, Genetics, Pathology and Forensic Medicine, Clinical Biochemistry and Cancer Research, having authored 33 papers that have together received 1.2k indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (7 papers), Connective tissue disorders research (6 papers), Genetic factors in colorectal cancer (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Cancer Genomics and Diagnostics (4 papers), Hedgehog Signaling Pathway Studies (3 papers), BRCA gene mutations in cancer (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Developmental Biology (97 citations), Pathology and Forensic Medicine (398 citations), Genetics (444 citations), Cancer Research (208 citations) and Rheumatology (151 citations). Timm O. Goecke has collaborated with scholars based in Germany, United States and Türkiye. Frequent co-authors include F. Majewski, John M. Opitz, Christoph Engel, Gabriela Möslein, Karsten Schulmann, Frank Majewski, Wolfgang Küster, Matthias Kloor, Markus Loeffler and Hans K. Schackert. Their work appears in journals such as Human Genetics, European Journal of Pediatrics, European Journal of Human Genetics, Movement Disorders and European Journal of Cancer Prevention.

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