Evidence map›Paper›PMID 22426219›Full record

ArticleNature communications2012

New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing.

Andreas Keller, Angela Graefen, Markus Ball, Mark Matzas, Valesca Boisguerin, Frank Maixner, Petra Leidinger, Christina Backes, Rabab Khairat, Michael Forster and 31 more

Open access · hybridAbstract readHistorical Article
PubMed Publisher
In one paragraph

Article in Nature communications, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 187 papers.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed
34.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

187 citing papers in PubMed, 458 citations in OpenAlex.

  1. Review
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127 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

41 authors at 15 institutions in 8 countries.

Andreas KellerDepartment of Human Genetics, Saarland University, 66421 Homburg, Saar, Germany.
Angela Graefen
Markus Ball
Mark Matzas
Valesca Boisguerin
Frank Maixner
Petra Leidinger
Christina Backes
Rabab Khairat
Michael Forster
Björn Stade
Andre Franke
Jens Mayer
Jessica Spangler
Stephen McLaughlin
Minita Shah
Clarence Lee
Timothy T Harkins
Alexander Sartori
Andres Moreno-Estrada
Brenna Henn
Martin Sikora
Ornella Semino
Jacques Chiaroni
Siiri Rootsi
Natalie M Myres
Vicente M Cabrera
Peter A Underhill
Carlos D Bustamante
Eduard Egarter Vigl
Marco Samadelli
Giovanna Cipollini
Jan Haas
Hugo Katus
Brian D O'Connor
Marc R J Carlson
Benjamin Meder
Nikolaus Blin
Eckart Meese
Carsten M Pusch
Albert Zink
Eurac Research · ITSaarland University · DEStanford University · USHeidelberg University · DEKiel University · DEUniversity of Tübingen · DEBioMed X Institute · DECentre National de la Recherche Scientifique · FREstonian Biocentre · EEFred Hutch Cancer Center · USNCR (United States) · USOspedale di Bolzano · ITUniversidad de La Laguna · ESUniversity of Pavia · ITWroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Tyrolean Iceman, a 5,300-year-old Copper age individual, was discovered in 1991 on the Tisenjoch Pass in the Italian part of the Ötztal Alps. Here we report the complete genome sequence of the Iceman and show 100% concordance between the previously reported mitochondrial genome sequence and the consensus sequence generated from our genomic data. We present indications for recent common ancestry between the Iceman and present-day inhabitants of the Tyrrhenian Sea, that the Iceman probably had brown eyes, belonged to blood group O and was lactose intolerant. His genetic predisposition shows an increased risk for coronary heart disease and may have contributed to the development of previously reported vascular calcifications. Sequences corresponding to ~60% of the genome of Borrelia burgdorferi are indicative of the earliest human case of infection with the pathogen for Lyme borreliosis.

Indexed as

Genome, HumanGenome, MitochondrialMummiesBase SequenceBorrelia burgdorferiChromosome MappingDNA, MitochondrialGenetic Predisposition to DiseaseHistory, AncientHumansLyme DiseaseMitochondriaPaleontologyPhenotypeSequence Analysis, DNAVascular CalcificationDNA, Mitochondrial

Identifiers

PMID22426219
OpenAlexW2090819968

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.