LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia (Q24324059)

GOA release 2020-03-11

M Groszer

8

0 references

Stefano Colella

S Colella

7

0 references

Antonio Velayos-Baeza

A Velayos-Baeza

5

0 references

Clyde Francks

C Francks

1

0 references

Richard Wade-Martins

R Wade-Martins

32

0 references

Kenneth Kendler

38

K S Kendler

0 references

David St Clair

28

D St Clair

0 references

Hans-Jürgen Möller

26

H-J Möller

0 references

author name string

S Maegawa

2

0 references

J Laurén

3

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B S Abrahams

4

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S E Medland

6

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E Z McAuley

9

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T M Caffrey

10

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T Timmusk

11

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P Pruunsild

12

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I Koppel

13

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P A Lind

14

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N Matsumoto-Itaba

15

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J Nicod

16

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L Xiong

17

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R Joober

18

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W Enard

19

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B Krinsky

20

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E Nanba

21

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A J Richardson

22

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B P Riley

23

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N G Martin

24

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S M Strittmatter

25

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D Rujescu

27

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P Muglia

29

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J L Roos

30

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S E Fisher

31

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G A Rouleau

33

0 references

J F Stein

34

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M Karayiorgou

35

0 references

D H Geschwind

36

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J Ragoussis

37

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M S Airaksinen

39

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M Oshimura

40

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L E DeLisi

41

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A P Monaco

LRRTM3 promotes processing of amyloid-precursor protein by BACE1 and is a positional candidate gene for late-onset Alzheimer's disease

42

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language of work or name

English

0 references

publication date

December 2007

0 references

published in

Molecular Psychiatry

0 references

volume

12

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issue

12

0 references

page(s)

1129-39, 1057

0 references

cites work

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Accelerated evolution of Protocadherin11X/Y: a candidate gene-pair for cerebral asymmetry and language

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Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1

27 September 2017

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Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

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Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness

27 September 2017

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29 November 2018

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29 November 2018

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29 November 2018

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29 November 2018

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29 November 2018

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Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

29 November 2018

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Family-based association study of markers on chromosome 22 in schizophrenia using African-American, European-American, and Chinese families

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2990633

Localized morphological brain differences between English-speaking Caucasians and Chinese-speaking Asians: new evidence of anatomical plasticity

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2990633

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29 November 2018

1 reference

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29 November 2018

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Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

29 November 2018

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29 November 2018

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Schizophrenic patients and their first-degree relatives show an excess of mixed-handedness

29 November 2018

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The recycling pathway of protein ERGIC-53 and dynamics of the ER-Golgi intermediate compartment

29 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/17667961

12 December 2020

inferred from PubMed ID database lookup

Hand preference and hand skill in families with schizophrenia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17667961

12 December 2020

inferred from PubMed ID database lookup

Epigenetic heterogeneity at imprinted loci in normal populations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17667961

12 December 2020

inferred from PubMed ID database lookup

Genetics of Cognition: Outline of a Collaborative Twin Study

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.MP.4002053

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.MP.4002053

1 reference

Dimensions Publication ID

1034646284

0 references

1 reference

1 reference

PubMed publication ID

17667961

1 reference