Niels Morling

ORCID: 0000-0002-9463-5087
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About
Contact & Profiles
Research Areas
  • Forensic and Genetic Research
  • Molecular Biology Techniques and Applications
  • Genetic diversity and population structure
  • T-cell and B-cell Immunology
  • Genetic Associations and Epidemiology
  • Race, Genetics, and Society
  • Genomics and Phylogenetic Studies
  • Immune Cell Function and Interaction
  • Environmental DNA in Biodiversity Studies
  • Immunodeficiency and Autoimmune Disorders
  • RNA and protein synthesis mechanisms
  • melanin and skin pigmentation
  • Epigenetics and DNA Methylation
  • Gene expression and cancer classification
  • Skin Protection and Aging
  • Forensic Anthropology and Bioarchaeology Studies
  • Systemic Lupus Erythematosus Research
  • Genetic and phenotypic traits in livestock
  • Identification and Quantification in Food
  • Immunotherapy and Immune Responses
  • Biochemical Analysis and Sensing Techniques
  • Blood groups and transfusion
  • Cardiac electrophysiology and arrhythmias
  • RNA modifications and cancer
  • RNA Research and Splicing

University of Copenhagen
2016-2025

Aalborg University
2019-2025

Universidade de Santiago de Compostela
2017

Rigshospitalet
1984-2016

Oslo University Hospital
2016

Kennedy Center
2016

Copenhagen University Hospital
1976-2016

Institut National de Criminalistique et de Criminologie
2015

Technical University of Denmark
2012

Hvidovre Hospital
1978-2011

A total of 52 SNPs reported to be polymorphic in European, Asian and African populations were selected. Of these, 42 from the distal regions each autosome (except chromosome 19). Nearly all selected located at least 100 kb distant known genes commonly used STRs. We established a highly sensitive reproducible SNP-typing method with amplification DNA fragments one PCR reaction followed by detection two single base extension reactions analysed using CE. The amplicons ranged 59 115 bp length....

10.1002/elps.200500671 article EN Electrophoresis 2006-04-03
Kaye N. Ballantyne Arwin Ralf Rachid Aboukhalid Niaz M. Achakzai Maria João Anjos and 95 more Qasim Ayub Jože Balažič Jack Ballantyne David Ballard Burkhard Berger Cecilia Bobillo Mehdi Bouabdellah Haran Burri Tomas Capal Stefano Caratti Jorge Cárdenas François Cartault Elizeu Fagundes de Carvalho M. Carvalho Baowen Cheng Michael D. Coble David Comas Daniel Corach María Eugenia D’Amato Sean Davison Peter de Knijff Maria Corazon A. De Ungria Ronny Decorte Tadeusz Dobosz Berit Myhre Dupuy Samir Elmrghni Mateusz Gliwiński Sara C. Gomes Laurens J.W. Grol Cordula Haas Erin Hanson Jürgen Henke Lotte Henke Fabiola Herrera-Rodríguez Carolyn R. Hill Gunilla Holmlund Katsuya Honda Uta‐Dorothee Immel Shota Inokuchi Mark A. Jobling Mahmoud Kaddura Jong S. Kim Soon H Kim Wook Kim Turi King Eva Klausriegler Daniel Kling Lejla Kovačević Leda Kovatsi Paweł Krajewski С. А. Кравченко Maarten Larmuseau Eun Young Lee Р. Лессиг Л. А. Лившиц Damir Marjanović Marek Minárik Natsuko Mizuno Helena Moreira Niels Morling Meeta Mukherjee Patrick Munier Javaregowda Nagaraju Franz Neuhuber Shengjie Nie Premlaphat Nilasitsataporn Takeki Nishi Hye Hyun Oh Jill K. Olofsson Valerio Onofri Jukka U. Palo Horolma Pamjav Walther Parson Michal Petlach Christopher Phillips Rafał Płoski Samayamantri P. R. Prasad Dragan Primorac Gludhug A. Purnomo Josephine Purps Héctor Rangel‐Villalobos Krzysztof Rębała Budsaba Rerkamnuaychoke Danel Rey González Carlo Robino Lutz Roewer Alexandra Rosa Antti Sajantila Andrea Sala Jazelyn M. Salvador Paula Sanz Cornelia Schmitt Añil Sharma Silva Da Kyoung‐Jin Shin

Relevant for various areas of human genetics, Y-chromosomal short tandem repeats (Y-STRs) are commonly used testing close paternal relationships among individuals and populations, male lineage identification. However, even the widely 17-loci Yfiler set cannot resolve populations completely. Here, 52 centers generated quality-controlled data 13 rapidly mutating (RM) Y-STRs in 14,644 related unrelated males from 111 worldwide populations. Strikingly, >99% 12,272 were completely individualized....

10.1002/humu.22599 article EN Human Mutation 2014-06-11
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