Evidence map›Paper›PMID 16380906›Full record

ArticleAmerican journal of human genetics2005

Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.

Tadao Arinami, Tsuyuka Ohtsuki, Hiroki Ishiguro, Hiroshi Ujike, Yuji Tanaka, Yukitaka Morita, Mari Mineta, Masashi Takeichi, Shigeto Yamada, Akira Imamura and 43 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 96 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. miR-137: a new player in schizophrenia.International journal of molecular sciences · 2014
    Review
  13. Neurobiology of schizophrenia onset.Current topics in behavioral neurosciences · 2014
    Review
  14. Article
  15. Article
  16. Article
  17. Deletion of PLCB1 gene in schizophrenia-affected patients.Journal of cellular and molecular medicine · 2012
    Article
  18. Article
  19. Article
  20. Article
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

53 authors at 20 institutions in 1 country.

Tadao ArinamiDepartment of Medical Genetics, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Ibaraki-ken, 305-8577, Japan. tarinami@md.tsukuba.ac.jp
Tsuyuka Ohtsuki
Hiroki Ishiguro
Hiroshi Ujike
Yuji Tanaka
Yukitaka Morita
Mari Mineta
Masashi Takeichi
Shigeto Yamada
Akira Imamura
Koichi Ohara
Haruo Shibuya
Kenshiro Ohara
Yasuo Suzuki
Tatsuyuki Muratake
Naoshi Kaneko
Toshiyuki Someya
Toshiya Inada
Takeo Yoshikawa
Tomoko Toyota
Kazuo Yamada
Takuya Kojima
Sakae Takahashi
Ohmori Osamu
Takahiro Shinkai
Michiko Nakamura
Hiroshi Fukuzako
Tomo Hashiguchi
Shin-ich Niwa
Takuya Ueno
Hirokazu Tachikawa
Takafumi Hori
Takashi Asada
Shinichiro Nanko
Hiroshi Kunugi
Ryota Hashimoto
Norio Ozaki
Nakao Iwata
Mutsuo Harano
Heii Arai
Tohru Ohnuma
Ichiro Kusumi
Tsukasa Koyama
Hiroshi Yoneda
Yasuyuki Fukumaki
Hiroki Shibata
Sunao Kaneko
Hisashi Higuchi
Norio Yasui-Furukori
Yohtaro Numachi
Masanari Itokawa
Yuji Okazaki
Japanese Schizophrenia Sib-Pair Linkage Group
University of Tsukuba · JPHirosaki University · JPNiigata University · JPOkayama University · JPSaga University · JPFujita Health University · JPFukushima Medical University · JPHokkaido University · JPJuntendo University Hospital · JPKyushu University · JPNihon University · JPTeikyo University Hospital · JPUniversity of Occupational and Environmental Health Japan · JPKagoshima University · JPKurume University · JPMie University · JPNagasaki University · JPNagoya University · JPOsaka University of Pharmaceutical Sciences · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Japanese Schizophrenia Sib-Pair Linkage Group (JSSLG) is a multisite collaborative study group that was organized to create a national resource for affected sib pair (ASP) studies of schizophrenia in Japan. We used a high-density single-nucleotide-polymorphism (SNP) genotyping assay, the Illumina BeadArray linkage mapping panel (version 4) comprising 5,861 SNPs, to perform a genomewide linkage analysis of JSSLG samples comprising 236 Japanese families with 268 nonindependent ASPs with schizophrenia. All subjects were Japanese. Among these families, 122 families comprised the same subjects analyzed with short tandem repeat markers. All the probands and their siblings, with the exception of seven siblings with schizoaffective disorder, had schizophrenia. After excluding SNPs with high linkage disequilibrium, we found significant evidence of linkage of schizophrenia to chromosome 1p21.2-1p13.2 (LOD=3.39) and suggestive evidence of linkage to 14q11.2 (LOD=2.87), 14q11.2-q13.2 (LOD=2.33), and 20p12.1-p11.2 (LOD=2.33). Although linkage to these regions has received little attention, these regions are included in or partially overlap the 10 regions reported by Lewis et al. that passed the two aggregate criteria of a meta-analysis. Results of the present study--which, to our knowledge, is the first genomewide analysis of schizophrenia in ASPs of a single Asian ethnicity that is comparable to the analyses done of ASPs of European descent--indicate the existence of schizophrenia susceptibility loci that are common to different ethnic groups but that likely have different ethnicity-specific effects.

Indexed as

Chromosomes, Human, Pair 1Chromosomes, Human, Pair 14Chromosomes, Human, Pair 20Genetic LinkagePolymorphism, Single NucleotideGenetic MarkersGenetic Predisposition to DiseaseGenome, HumanHumansJapanLod ScoreMicrosatellite RepeatsPedigreeSchizophreniaSiblingsGenetic Markers

Identifiers

PMID16380906
PMCPMC1285184
OpenAlexW2108715835

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.