D-Index & Metrics Best Publications
Genetics
Germany
2023
Genetics and Molecular Biology
Germany
2022

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 147 Citations 101,405 1,012 World Ranking 684 National Ranking 26
Genetics D-index 147 Citations 99,763 910 World Ranking 89 National Ranking 7

Research.com Recognitions

Awards & Achievements

2023 - Research.com Medicine in Germany Leader Award

2023 - Research.com Genetics in Germany Leader Award

2022 - Research.com Genetics and Molecular Biology in Germany Leader Award

Overview

What are the main themes of his work throughout his whole career to date

His study deals with a combination of Gene and Bioinformatics. Markus M. Nöthen integrates several fields in his works, including Bioinformatics and Gene. In his study, he carries out multidisciplinary Single-nucleotide polymorphism and Genome-wide association study research. Markus M. Nöthen integrates Genome-wide association study and Single-nucleotide polymorphism in his research. With his scientific publications, his incorporates both Genotype and Genetic predisposition. Markus M. Nöthen integrates many fields in his works, including Genetic predisposition and Genotype. He brings together Genetic association and Allele to produce work in his papers. Markus M. Nöthen incorporates Allele and Genetic association in his studies. His Genetics study frequently draws connections between adjacent fields such as Antibody.

Markus M. Nöthen most often published in these fields:

  • Gene (100.00%)
  • Single-nucleotide polymorphism (100.00%)
  • Genotype (100.00%)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj.
Nature Genetics (2013)

3630 Citations

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)

2992 Citations

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Nature Genetics (2009) 41 (1088-1093))

D Harold;R Abraham;P Hollingworth;R Sims.
Nature Genetics (2013)

2857 Citations

Genome-wide association study identifies five new schizophrenia loci

Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)

2508 Citations

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)

2097 Citations

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Heribert Schunkert;Inke R. König;Sekar Kathiresan;Muredach P. Reilly.
Nature Genetics (2011)

1965 Citations

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira.
Nature Genetics (2012)

1960 Citations

Large recurrent microdeletions associated with schizophrenia

Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
Nature (2008)

1907 Citations

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.

Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)

1904 Citations

Defining the role of common variation in the genomic and biological architecture of adult human height

Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)

1899 Citations

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