Ralf Sudbrak - Concepedia

Author

Ralf Sudbrak

Max Planck Institute for Molecular Genetics ORCID

Also Known As

A. Fujiyama, Christie Kovar, Clarence C. Lee, Horvath, Judit, Jerilyn A. Walker, Norman P. Gerry, R Sudbrak, R. SUDBRAK, R. Sudbrak, RALF SUDBRAK

Publications

87.7K

Citations

H-Index

Concepts

All Affiliations

Max Planck Institute for Molecular Genetics Max Planck Society Centre for Human Genetics University of Oxford Ludwig-Maximilians-Universität München

About

Ralf Sudbrak is an author at Max Planck Institute for Molecular Genetics specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	6.5K
2	Engineering	1	1	19
3	Health Sciences	1	1	14
4	Natural Sciences	1	1	208
5	Public Health	1	1	22

Ralf Sudbrak

Publications

9.2K

Citations

H-Index

Page 1

	Year	Citations
Transcriptome and genome sequencing uncovers functional variation in humans Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer, Nature Human VariationGeneticsGenomicsTranscriptomicsMedicine	2013	2.1K
The DNA sequence of the human X chromosome Mark T. Ross, Darren Grafham, Alison J. Coffey, Nature ChromatinDnaGeneticsChromosome BiologyMolecular Genetics	2005	1.2K
A global reference for human genetic variation Adam Auton, Gonçalo R. Abecasis, David Altshuler, Civil War Book Review	2015	612
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry Heike Olbrich, Karsten Häffner, Andreas Kispert, Nature Genetics Genome InstabilityMendelian DisorderGenetic DisorderGeneticsPathology	2002	550
A map of human genome variation from population-scale sequencing Richard Durbin, David L. Altshuler, Gonçalo R. Abecasis, HAL (Le Centre pour la Communication Scientifique Directe)	2010	542
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure Ralf Birkenhäger, Edgar A. Otto, Maria J. Schürmann, Nature Genetics UrologyMendelian DisorderGenetic DisorderKidney FailurePathology	2001	529
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel Olivier Delaneau, Jonathan Marchini, Gil McVean, Nature Communications Haplotype DeterminationNext-generation SequencingGeneticsGenomes ProjectArray Data	2014	441
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin Edgar A. Otto, Bart Loeys, Hemant Khanna, Nature Genetics Mendelian DisorderAutoimmune DiseaseGenetic DisorderGeneticsPathology	2005	401
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Heike Olbrich, Manfred Fliegauf, Julia Hoefele, Nature Genetics Ocular DiseaseMendelian DisorderNovel GeneOphthalmologyGenetic Disorder	2003	364
<i>DNAH5</i> Mutations Are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects Nada Hornef, Heike Olbrich, Judit Horváth, American Journal of Respiratory and Critical Care Medicine	2006	342

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