The overwhelming majority of variants which The Koreans only carry have relation to brain and mental diseases

NCBI search results for gene with variants which The Korean only carry

SNV-1= SNVs (single nucleotide variant) detected in Korean individuals but not included in others (Europeans, The Chinese, The Japanese etc)


 1.brain 2.testis


1.brain 2.kidney

1.brain 2.stomatch

1.brain 2.heart

1.brain 2.prostate


1.brain 2.testis


1.brain 2.adrenal

1.brain 2.endometrium

1.brain 2.adrenal

1.brain 2.testis

1.brain 2.thyroid

1.brain 2.prostate

1.brain 2.others

1.brain


1.brain 2.adrenal


1.brain 2.lung

And so on ......

The above graphs which were shown in the NCBI search results indicates the body parts associated with gene which are variants(=mutation) that Koreans only carry, and the targeting gene symbol names used for the NCBI searching are a list of gene names with Korean-specific genetic mutations extracted from the following paper.

It is very clear thing that the genes in which Korean-specific variants have occurred are related to the brain in the human body parts.

population genetics paper #1 (FDA)

Whole genome sequencing of 35 individuals provides insights into the genetic structure of Korean population
Wenqian Zhang et al.
Supplementary Table S5:
A list of genes involved in Korean SNV-1 and the SNV count per gene.

SYMBOL Gene Name	# of SNVs
PRIM2 please see below	5033
Y_RNA Y chromosome	3300
CSMD1 please see above	1786
snoU13 No items found in NCBI	1731
PDE4DIP please see above	1374
RBFOX1 please see above	1272
PTPRN2 please see above	1224
KMT2C please see bellow	1091
PTPRD please see above	1084
LINC00842 please see below	1008
and so on	and so on

 

1.prostate

various

1.skin 2.liver

Answer by Google AI for gene with variants which The Korean only carry

The PRIM2 gene has been identified as a key player in the genetic basis of insomnia. Research has shown that PRIM2, along with other genes like RPA2, ORC6, and PIAS3, are core nodes in brain regions associated with insomnia. Studies have linked PRIM2 to the prenatal dorsolateral prefrontal cortex, inferolateral temporal cortex, medial prefrontal cortex, and amygdala, suggesting its role in regulating sleep-wake cycles and sleep disturbances. Additionally, research suggests a strong genetic component to insomnia, with studies indicating that genetics and epigenetics contribute to its development.





Please note that the crucial point is that CSMD1 gene have relation to synaptic pruning.

1.The excessive synaptic pruning is the pathogenetic basis of schizophrenia.
2.The insufficient synaptic pruning is the pathogenetic basis of autism spectrum disorder (ASD).
3. The inadequate or irregular synaptic pruning is the basis of other psychiatric disorders.

And, we, humans around the world should know the very simple fact that The Koreans have a huge number of peculiar mutations in CSMD1 gene.



Small nucleolar RNAs (snoRNAs) are a class of non-coding RNAs that play a role in various diseases, including psychiatric disorders. Studies have shown that alterations in snoRNA expression are linked to conditions like autism spectrum disorder (ASD), schizophrenia, and major depressive disorder (MDD). snoRNAs can influence brain function and behavior by regulating gene expression and other cellular processes.

Here's a more detailed look:

1. SnoRNAs and Psychiatric Disorders:

Autism Spectrum Disorder (ASD):
Research suggests that dysregulated snoRNA expression in both blood and brain tissues is correlated with changes in synaptic gene functions in ASD.

Schizophrenia (SCZ):
While studies on snoRNAs in SCZ are still ongoing, some research indicates that snoRNAs may be involved in the disease's pathophysiology, potentially through sex-based dysregulation in the brain.

Major Depressive Disorder (MDD):
Several studies have identified snoRNAs associated with MDD, some using brain tissue and others using both brain tissue and blood samples.

Bipolar Disorder:
One study suggests that snoRNAs may be associated with bipolar disorder.

2. How SnoRNAs Influence the Brain:
Gene Regulation:
snoRNAs can influence alternative splicing and epigenomic and epitranscriptomic modifications, affecting cell proliferation, differentiation, and neurotransmission.

Synaptic Function:
Dysregulated snoRNA expression can impact synaptic gene functions, which are important for communication between neurons.

Neurotransmitter Regulation:
Some snoRNAs have been shown to affect neurotransmitter pathways, which are important for mood regulation and other mental processes.

Omitted below

 
The RBFOX1 gene has been linked to various mental disorders, including autism spectrum disorder (ASD), schizophrenia, and other neurodevelopmental conditions. RBFOX1 encodes a protein that regulates gene expression, and variations in this gene can disrupt normal brain development, contributing to the development of these disorders.

Mechanism of Action:
RBFOX1 acts as a splicing factor, meaning it regulates the process of how genes are expressed. Disruptions in this process can lead to abnormal brain function and contribute to the development of mental disorders.


The PDE4DIP gene, also known as Myomegalin (MMGL), has been linked to various mental health conditions, particularly in studies involving Alzheimer's disease (AD), vascular dementia (VaD), and frontotemporal dementia (FTD). Dysregulation of PDE4DIP expression is considered a potential early event that may contribute to the development of these dementias. Additionally, PDE4DIP has been implicated in schizophrenia and bipolar disorder.

And so on ......

My investigation results completely consistent with NCBI and Google AI.

Although there is no exact data, please don't misunderstand that the prevalence rates of schizophrenia are high among Koreans compared with other ethnic populations

>

gene	# of SNVs	Related papers
PRIM2	5033	insomnia paper[86] Schizophrenia paper[103]
CSMD1	1786	Schizophrenia paper[9] paper[52] paper[115] paper[116] paper[141] paper[142] paper[148] paper[165] paper[178] paper[181] bipolar paper[66] paper[148] paper[165] paper[116] autism paper[137] cognitive ability paper[138] Amygdala in brain paper[139] rs10503253 Schizophrenia,Memory and learning ability paper[140] neurodevelopmental disorders （DSM-5） paper[179]
snoU13 =snoRNAs U13	1731	=gene symbol name means Small nucleolar RNAs (snoRNAs) U13 depression, insomnia paper[43]
PDE4DIP	1374	mental disorders paper[4] paper[177] depression, paper[91] dementia paper[119] synapse paper[173]
RBFOX1	1272	intelligence paper[168] paper[169] insomnia paper[161] autism paper[165] anger,aggression,autism paper[100] Schizophrenia paper[5] paper[167] depression, Schizophrenia, neurosis paper[121] Personality, alcoholism, paper[122] ADHD paper[123] paper[182] aggressive behavior paper[124] Schizophrenia (the neuronspecific RNA splicing regulator) paper[125] Many other related papers
PTPRN2	1224	Personality disorders paper[99] depression paper[6] Schizophrenia, ADHD paper[126]
KMT2C	1091	intelligence paper[159] bipolar paper[7] paper[130] Schizophrenia paper[128]   depression paper[129]
PTPRD	1084	insomnia paper[161] intelligence paper[159] paper[168] ADHD paper[165] bipolar paper[165] Personality disorders paper[8] paper[165] paper[127] Schizophrenia, synaptic adhesion paper[125] intellectual disability, anxiety, Personality disorders paper[127] autism paper[137] Personality disorders paper[143] Neuroticism paper[143]
LINC00842	1008	0
CNTNAP2	940	intellectual disability, autism paper[109] Schizophrenia paper[10] paper[165] mental disorders,language development disorder paper[131] paper[175] Personality disorders paper[176]
ROBO2	932	Schizophrenia, depression paper [13] autism paper [117]
ZNF717	859	intellectual disability paper[14] psychoneurosis  paper[93] brain paper[94] autism paper[132]
CROCC	844	0
AF146191	800	insomnia paper[101]
LSAMP	800	insomnia paper[161] suicide paper[15] bipolar paper[165]
WWOX	797	mentally retardation paper[81] autism paper[165]
DLG2	789	Schizophrenia paper[5]
GUSBP1	760	0
EYS	759	Schizophrenia paper[5] bipolar paper[160]
ANKRD30BL	730	0
PCDHA1 ～ PCDHA14	710	Schizophrenia paper[166]
MACROD2	693	intelligence paper[168] paper[169] autism paper[165] bipolar paper[5] depression paper[158]
DPP6	681	neurodevelopmental disorders paper[89]
LRP1B	677	intelligence paper[159] cognitive ability paper[5] Schizophrenia paper[165]
TPTE	664	intelligence paper[159] depression paper[110]
ANKRD36C	653	0 paper[112] Alzheimer’s Disease
PCDH15	645	cognitive ability paper[114] Schizophrenia・autism paper[82] ADHD paper[182]
FHIT	642	Schizophrenia paper[5] paper[165]
LINC00969	640	Schizophrenia paper[57]
KCNJ12	626	depression paper[113]
BAGE2	618	0 paper[146] Alzheimer’s Disease
UPK3B	608	0
CTNNA3	605	Schizophrenia paper[165] autism paper[79] impulsive behavior paper[172] effectiveness of antidepressants paper[98]
NRXN3	602	neuropsychiatric disease paper[80] autism paper[117]
CDH13	600	autism, Schizophrenia, bipolar, depression, ADHD paper[16] paper[64] Schizophrenia, ADHD paper[165] Personality disorders paper[176]
SGCZ	582	intelligence paper[168] depression paper[73]
CNTN5	568	suicide paper[74]
PARK2	568	intelligence paper[159] intellectual disability, autism paper[109] Personality disorders paper[75]
MAP2K3	564	General mental deseases paper[76] autism paper[146]
CCSER1	564	0 alcoholism paper[77]
GRID2	561	0 stress  paper[78]
CTNNA2	553	intelligence paper[168] educational attainment paper[5] impulsive behavior paper[172]
DAB1	528	insomnia paper[161] mentally retardation paper[44] Schizophrenia paper[165]
GPC5	527	intelligence paper[159] cognitive ability paper[45]
NAALADL2	519	autism paper[46]
MAGI2	50MAGI26	Schizophrenia, depression [paper[47] Personality [paper[75] Schizophrenia, synaptic adhesion paper[125] paper[165]
DPP10	505	Neurodevelopmental disorders paper[177] ADHD paper[48]
PDE4D	503	intelligence paper[168] paper[169] personal disorder paper[49] synapse paper[173]
KCNIP4	497	Personality disorders, ADHD paper[50]
CNTN4	485	intellectual disability, autism paper[109] paper[177] Schizophrenia paper[40] paper[165] autism paper[137] bipolar paper[160]
TBC1D5	478	paper[51] bipolar
AGBL4	474	paper[52] cognitive ability
ASIC2	471	paper[52] Schizophrenia
CADM2	471	intelligence paper[118] paper[168] General mental deseases paper[38] cognitive ability paper[88]
CDH12	469	Schizophrenia, bipolar, depression paper[24]
ZDHHC11	468	intelligence paper[159]
ADARB2	468	autism paper[53]
DCC	467	intelligence paper[135] paper[168] paper[169] insomnia paper[161] cognitive ability paper[5] ADHD, depression paper[134] paper[162] autism paper[162] depression paper[136] paper[137] paper[174] Schizophrenia paper[162] impulsive behavior paper[171] paper[172] brain capacity paper[164]
GALNTL6	459	intelligence paper[159]
ANKRD36	458	0 alcoholism paper[54]
CDH4	457	intelligence paper[168] Schizophrenia paper[25]
PRR4	457	Schizophrenia paper[55]
LRRC4C	448	intelligence paper[159] anorexia paper[5] Schizophrenia, synaptic adhesion paper[125]
MIR44351HG	445	0
LINC00960	443	Schizophrenia paper[56]
SLC9B1P4	442	0
PTPRT	434	intelligence paper[168] paper[169] intellectual disability paper[58] autism paper[165]
SDK1	431	insomnia paper[161] child abuse paper[59] Personality disorders paper[176]
PARD3B	430	intelligence paper[159] Personality disorders paper[60]
SLC9B1P1	425	0
TAS2R14	421	0
RUNX1	420	mentally retardation paper[61]
AUTS2	420	intelligence paper[168] paper[169] intellectual disability, autism paper[111] Schizophrenia,autism paper [42],[53]
CSMD3	418	autism paper[62] neurodevelopmental disorders （DSM-5） paper[180]
NRXN1	418	intelligence paper[159] intellectual disability, autism paper[109] autism, Schizophrenia paper[35] paper[95] autism paper[117] Schizophrenia, synaptic adhesion paper[125] mental disorders,Schizophrenia,autism paper[131] paper[167]
LINC00955	418	0
ZNF385D	418	Schizophrenia paper[63]
PRKG1	417	ADHD paper[64] impulsive behavior paper[172]
CAMTA1	416	intelligence paper[159] paper[169] memory ability paper[65]
SPAG16	414	bipolar paper[66] paper[156]
TMEM132D	410	intelligence paper[159] personarity disorder paper[67] anxiety paper[165]
ROBO1	409	math ability paper[68]
GPC6	408	autism paper[69] paper[137]
NBPF1	407	brain capacity paper[92]
LRRTM4	406	tourette syndrome paper[70]
	405	brain capacity ppaper[71] brain paper[105]
NCOR1P2	402	0
TTC34	400	0
NKAIN2	398	intelligence paper[72] Schizophrenia paper[72]
SMYD3	397	mentally retardation paper[41]
RPTOR	395	intelligence paper[159] Schizophrenia paper[40]
AC090044.1	394	0
OPCML	390	Schizophrenia paper[37] paper[165]
SNX29	390	intelligence paper[168] paper[169] insomnia paper[161] educational attainment paper[5] autism paper[26]
NRG1	388	ADHD paper[2] bipolar paper[104] Schizophrenia paper[11]paper[87] Schizophrenia, synaptic plasticity related genes paper[125]
ERBB4	387	intelligence paper[159] Schizophrenia paper[36] autism paper[117]
ERC2	386	autism,Schizophrenia paper[35] Schizophrenia, ADHD paper[126]
NTM	385	insomnia paper[161] intelligence paper[34]
SRGAP2B	383	Brain development paper[83]
SLC9B1P3	383	0
CNTNAP3B	379	cognitive ability paper[39] Appendix 4
GRM7	379	bipolar paper[33]
CACNA2D3	379	Schizophrenia paper[32] paper[125] Personality disorders paper[176]
MIR663A	376	0
SNTG1	376	cerebral cortex paper[163]
SUMF1	374	mentally retardation paper[31]
SORCS2	373	bipolar, paper[30] paper[165]
DMD	373	autism paper[117]
HYDIN	372	brain capacity paper[85]
DGKB	372	cognitive ability paper[29]
NRG3	371	Schizophrenia paper[28] Schizophrenia,synaptic plasticity related genes paper[125]
FAM182B	369	0
TEKT4P2	368	0
DIP2C	367	General mental deseases paper[27]
AGBL1	366	autism paper[26]
CDH18	364	Schizophrenia,bipolar,depression paper[24]
HERC2P3	364	ADHD paper[23]
FRG2C	363	ADHD paper[23]
TRPM3	359	intellectual disability paper[22]
TRAPPC9	358	mentally retardation paper[21] intellectual disability paper[133]
ERICH1AS1	357	Schizophrenia paper[5]
DLGAP1	355	Schizophrenia paper[20]
HDAC9	354	Schizophrenia paper[19]
CTNND2	354	intelligence paper[159] intellectual disability paper[18]
C10orf11	351	cerebral cortex paper[163]
ASTN2	348	brain capacity paper[164] Schizophrenia, bipolar, autism paper[165]
CNTNAP5	340	bipolar paper[160]
PCDH9	330	intellectual disability, autism paper[109]
SHANK2	322	intellectual disability, autism paper[109] paper[109] paper[151] paper[152] paper[153] paper[154] depression paper[129] paper[157] autism, ADHD paper[149] neuropsychiatric disorders paper[150] ADHD paper[155]
FIP1L1	320	cerebral cortex paper[163]
EXOC4	320	intelligence paper[147] paper[135] paper[168] paper[169]
DPYD	319	Personality disorders paper[97] autism paper[117] intelligence paper[159] paper[168]
LARGE	317	intelligence paper[159] paper[168]
NEGR1	312	insomnia paper[161] intelligence paper[135] paper[147] paper[168] paper[169] depression paper[158]
CALN1	311	intelligence paper[159] paper[168] paper[169]
NPAS3	309	insomnia paper[161] intelligence paper[159] Schizophrenia paper[165]
THSD7B	306	intelligence paper[159] Personality disorders paper[176]
AGAP1	303	intelligence paper[159] paper[168] paper[169]
CACNA1C	302	autism paper[177] Schizophrenia paper[95] paper[141] paper[148] paper[166] paper[166] paper[181]

And so on ......

List of paper names

paper[1]
Rare coding variants in 10 genes confer substantial risk for schizophrenia.

Singh TJ et al.
Nature. April 6, 2022

paper[2]
an intriguing therapeutic target for neurodevelopmental disorders
Liang Shi & Clare M. Bergson
Nature Published: 16 June 2020

paper[3]
An interaction network of mental disorder proteins in neural stem cells
M J Moen et al,
Nature Published: 04 April 2017

paper[4]
Association between SNPs and gene expression in multiple regions of the human brain
S Kim et al,
Nature Published: 08 May 2012

paper[5]
Identification of pleiotropy at the gene level between psychiatric disorders and related traits
Tatiana Polushina et al,
Nature Published: 29 July 2021

[cited from the above paper]
Here, we aimed to identify genetic overlaps at the gene level between 7 mental disorders (schizophrenia, autism spectrum disorder, major depressive disorder, anorexia nervosa, ADHD, bipolar disorder and anxiety), 8 brain morphometric traits, 2 cognitive traits (educational attainment and general cognitive function) and 9 personality traits (subjective wellbeing, depressive symptoms, neuroticism, extraversion, openness to experience, agreeableness and conscientiousness, children’s aggressive behaviour, loneliness) based on publicly available GWASs.

paper[6]
A Genomewide Linkage Scan of Cocaine Dependence and Major Depressive Episode in Two Populations
BaoZhu Yang et ai.
Nature Published: 17 August 2011

paper[7]
Exome sequencing for bipolar disorder points to roles of de novo lossoffunction and proteinaltering mutations
M Kataoka et al.
Nature Published: 24 May 2016

paper[8]
Genomewide association study in obsessivecompulsive disorder: results from the OCGAS
M Mattheisen
Nature Published: 13 May 2014

paper[9]
The SchizophreniaAssociated Gene, CSMD1,Encodes a BrainSpecific Complement Inhibitor
Matthew L Baum
Harvard Libraly

paper[10]
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy
J I Friedman et al.
Nature Published: 24 July 2007

paper[11]
The molecular genetics of schizophrenia: new findings promise new insights M J Owen et al.
Nature Published: 28 October 2003

paper[12]
A genomewide investigation into parentoforigin effects in autism spectrum disorder identifies previously associated genes including SHANK3
Siobhan Connolly et al.
Nature Published: 23 November 2016


paper[13]
Convergence of evidence from a methylomewide CpGSNP association study and GWAS of major depressive disorder
Karolina A. Aberg et al.
Nature Published: 22 August 2018

[cited from the above paper]
ROBO2 (roundabout, axon guidance receptor, homolog 2) is critical for the maintenance of inhibitory synapses in the adult ventral tegmental area, a brain region important for the production of dopamine[41], and has been implicated in schizophrenia[42],[43],[44] and bipolar depression[45].

paper[14]
Identification of 11 potentially relevant gene mutations involved in growth retardation, intellectual disability, joint contracture, and hepatopathy
Hongyan Diao et al.
Published online 2018 Nov 16

paper[15]
Association of limbic systemassociated membrane protein (LSAMP) to male completed suicide
Anne Must et al.
Published: 23 April 2008

[cited from above paper]
According to the results of the current study, there might be a chance that variations in LSAMP gene play a role in pathoaetiology of suicidal behaviour.

paper[16]
The role of cadherin genes in five major psychiatric disorders: A literature update
Ziarih Hawi et al.
published: 18 September 2017

paper[17] Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11
Andreas Tzschach et al.
Nature Published: 21 October 2009

paper[18]
CTNND2— a candidate gene for reading problems and mild intellectual disability
Wolfgang Hofmeister et al.
February 3, 2015

paper[19]
HDAC9 is implicated in schizophrenia and expressed specifically in postmitotic neurons but not in adult neural stem cells
Bing Lang et al.
Published online 2011 Aug 18.

paper[20]
Genetic analysis of the DLGAP1 gene as a candidate gene for schizophrenia
JunMing Liet al
30 January 2013

paper[21]
Identification of Mutations in TRAPPC9, which Encodes the NIK and IKKβBinding Protein, in Nonsyndromic AutosomalRecessive Mental Retardation
Asif Mir et al.
11 December 2009

paper[22]
Diseaseassociated mutations in the human TRPM3 render the channel overactive via two distinct mechanisms
Siyuan Zhao et al.
eLife 2020

paper[23]
De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems
Erik A Ehli et al.
Nature Published: 11 April 2012

paper[24]
A novel relationship for schizophrenia, bipolar and major depressive disorder Part 5: a hint from chromosome 5 high density association screen
Xing Chen et al.
Published online 2017 May 15.


paper[25]
Neuronal cell adhesion genes Key players in risk for schizophrenia, bipolar disorder and other neurodevelopmental brain disorders?
Aiden P. Corvin
01 Oct 2010

paper[26]
Genomewide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders
Lu Xia et al.
published: 24 October 2019

paper[27]
Integrated multiomics reveal epigenomic disturbance of assisted reproductive technologies in human offspring
WeiChen et al.
Volume 61, November 2020

paper[28]
Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition
B Morar et al.
Nature
Published: 15 June 2010

paper[29]
Genetic Basis of a Cognitive Complexity Metric
Narell K. Hansell et al.
Published: April 10, 2015

[cited from the above paper] Abstract
Relational complexity (RC) is a metric reflecting capacity limitation in relational processing. It plays a crucial role in higher cognitive processes and is an endophenotype for several disorders. However, the genetic underpinnings of complex relational processing have not been investigated. Using the classical twin model, we estimated the heritability of RC and genetic overlap with intelligence (IQ), reasoning, and working memory in a twin and sibling sample aged 1529 years (N = 787). Further, in an exploratory search for genetic loci contributing to RC, we examined associated genetic markers and genes in our Discovery sample and selected loci for replication in four independent samples (ALSPAC, LBC1936, NTR, NCNG), followed by metaanalysis (N>6500) at the single marker level. Twin modelling showed RC is highly heritable (67%), has considerable genetic overlap with IQ (59%), and is a major component of genetic covariation between reasoning and working memory (72%). At the molecular level, we found preliminary support for four singlemarker loci (one in the gene DGKB), and at a genebased level for the NPS gene, having influence on cognition. These results indicate that genetic sources influencing relational processing are a key component of the genetic architecture of broader cognitive abilities. Further, they suggest a genetic cascade, whereby genetic factors influencing capacity limitation in relational processing have a flowon effect to more complex cognitive traits, including reasoning and working memory, and ultimately, IQ.

paper[30]
SorCS2 is required for BDNFdependent plasticity in the hippocampus
S Glerup el al.
Nature Published: 26 July 2016

paper[31]
Candidate genes for recessive nonsyndromic mental retardation on chromosome 3p (MRT2A)*
JJ Higgins et al
published: 18 May 2004

paper[32]
Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip
Tim Moons et al.
March 30, 2016

paper[33]
Allelic Association, DNA Resequencing and Copy Number Variation at the Metabotropic Glutamate Receptor GRM7 Gene Locus in Bipolar Disorder
Radhika Kandaswamy et al.
Accepted: 14 April 2014

paper[34]
NTM and NR3C2 polymorphisms influencing intelligence: Familybased association studies
Yue Pan et al.
Progress in NeuroPsychopharmacology & Biological Psychiatry 35 (2011) 154–160

paper[35]
CNTNAP2 and NRXN1 Are Mutated in AutosomalRecessive PittHopkinslike Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila
ChristianeZweier et al
13 November 2009,

paper[36]
Schizophrenia Candidate Gene ERBB4: Covert Routes of Vulnerability to Psychosis Detected at the Population Level
Nicholas C. Stefanis
March 2013

paper[37]
OPCML Gene as a Schizophrenia Susceptibility Locus in Thai Population
Benjaporn Panichareon
Published: 21 July 2011

paper[38]
Genetic variation in CADM2 as a link between psychological traits and obesity
Julia Morris et al
Nature Published: 14 May 2019

paper[39]
Ancient Migrations The first complete genome assembly, annotation and variants of the 2 ZoroastrianParsi community of India
Naseer Pasha et al
February 17, 2021

paper[40]
Altered DNA methylation associated with a translocation linked to major mental illness
Daniel L. McCartney et al.
Nature Published: 19 March 2018

[cited from the above paper] Twentytwo of the DMRs identified were within the major histocompatibility complex (MHC; Fig. 3), which has been implicated in the pathogenesis of SZ through a largescale GWAS.16 In addition, we identified DMRs within two additional genes (IGSF9B, CNTN4) that showed genomewide association with SZ in the same study.
Two additional DMRs were identified within genes associated with SZ at the genomewide significant level by the SZ Working Group of the Psychiatric Genomics Consortium (PGC).16 These were within the genes IGSF9B and CNTN4, both of which function as cell adhesion molecules. Two largescale epigenomewide association studies of SZ have recently been reported.12,13 These studies reported significant differential methylation in RPTOR: a gene in which we identified a DMR. RPTOR is a key component of mTOR signalling, which has been implicated in synaptic plasticity.36

paper[41]
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair
Dilek Aktas et al.
Published: 28 May 2010

paper[42]
Rare structural variants found in attentiondeficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
J Elia et al
Nature Published: 23 June 2009


paper[43]
GWAS MetaAnalysis Reveals Shared Genes and Biological Pathways between Major Depressive Disorder and Insomnia
YiSian Lin
Published: 26 September 2021

paper[44]
The Gene Encoding Disabled1 (DAB1), the Intracellular Adaptor of the Reelin Pathway, Reveals Unusual Complexity in Human and Mouse*
Isabelle Bar et al.
FEBRUARY 2003


paper[45]
Postaxial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR1792 and GPC5
P.Kannu et al.
8, August 2013

paper[46]
GenomeWide Association Study for Autism Spectrum Disorder in Taiwanese Han Population
PoHsiu Kuo et al.
2015 Sep 23

paper[47]
Genetic Dissection of Temperament Personality Traits in Italian Isolates Maria Pina Concas et al. 21 December 2021

paper[48]
Attention, cognitive control and motivation in ADHD: Linking eventrelated brain potentials and DNA methylation patterns in boys at early school age
Hartmut Heinrich et al
. Published: 19 June 2017

paper[49]
Association study of the PDE4D gene and obsessivecompulsive disorder in a Chinese Han population
Huang, Xing et al.
December 2019

paper[50]
KCNIP4 as a candidate gene for personality disorders and adult ADHD
LenaWeißflog et al. 2012.07.017

paper[51]
Implication of synapserelated genes in bipolar disorder by linkage and gene expression analyses
Catalina Lopez de Lara
2010 Jul 29

paper[52]
EpigenomeWide Association Study of Cognitive Functioning in MiddleAged Monozygotic Twins
Anna Starnawskal et al
12 December 2017

paper[52]
Host genetics influences the relationship between the gut microbiome and psychiatric disorders
ThaisMartinsSilva
2 March 2021

paper[53]
Identification of a functional rare variant in autism using genomewide screen for monoallelic expression
Eyal BenDavid et al
15 September 2011

paper[54]
Genomewide association study for maximum number of alcohol drinks in European Americans and African Americans
Ke Xu et al
2015 Jun 3

paper[55]
Sex differences in schizophrenia: a longitudinal methylome analysis
Christopher Adanty et al
Published: 30 December 2021

paper[56]
Long noncoding RNAassociated competing endogenous RNA axes in the olfactory epithelium in schizophrenia: a bioinformatics analysis
Hani Sabaie et al.
Nature Published: 30 December 2021

paper[57]
GenomeWide Search for SNP Interactions in GWAS Data: Algorithm, Feasibility, Replication Using Schizophrenia Datasets
KwanYeung Lee et al.
Nature 28 August 2020

paper[58]
Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) Contiguous Gene Syndromes by Chromosome Engineering in Mice: Phenotypic Consequences of Gene Dosage Imbalance
Katherina Walz 2003 May

paper[58]
Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing
Janneke H M SchuursHoeijmakers et al
February 13, 2014

paper[59]
Exposure to childhood abuse is associated with human sperm DNA methylation
Andrea L. Roberts et al.
Nature Published: 02 October 2018

paper[60]
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[notes]
# of SNVs in SNV1/ns is 21.
"# of SNVs in SNV35/ns" is 11.

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many thanks!


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