Related by context. All words. (Click for frequent words.) 58 recessive genes 57 recessive gene 55 autosomal recessive 55 autosomal dominant 54 recessive trait 52 mutated gene 51 recessive genetic 51 autosomal dominant disorder 50 autosomal recessive disorder 50 autosomal recessive disease 49 mutation 49 FMR1 gene 48 mutant gene 48 homozygous 48 homozygosity 48 germline mutations 48 incomplete penetrance 48 Angelman syndrome 48 premutation 48 FXTAS 48 heterozygous 47 genetically inherited 47 heritable 47 X chromosome 47 mosaicism 47 maternally inherited 47 recessive mutations 47 selfing 47 highly heritable 47 defective gene 47 Epidermolysis bullosa 47 de novo mutations 47 aY chromosome 47 Apert syndrome 47 nonhereditary 47 phenotype 46 Beckwith Wiedemann syndrome 46 recessive inheritance 46 Fragile X gene 46 inherited mutations 46 polygenic 46 recessive mutation 46 Lactose intolerance 46 Mendelian 46 maternally transmitted 46 polygynous 46 Klinefelter syndrome 45 autosomal 45 FASPS 45 ataxias 45 penetrance 45 microdeletion 45 maternally 45 spontaneous mutation 45 genetic abnormality 45 Tay Sachs disease 45 Male pattern baldness 45 phenotypically 45 chromosome abnormality 45 LIS1 45 inbreeding depression 45 gametophyte 45 recessive traits 45 MC1R 45 chromosomal abnormality 45 autosomal dominant inheritance 45 sexually dimorphic 45 inherited predisposition 44 galactosemia 44 APOE epsilon 4 44 polydactylism 44 HFE gene 44 dominantly inherited 44 familial adenomatous polyposis 44 nucleoli 44 germline cells 44 overo 44 APOE4 44 chromosomal deletions 44 phenotypes 44 genetic mutation 44 lymphocytic 44 allelic variants 44 heterozygote 44 polyploidy 44 polymorphism 44 orthologs 44 missense mutations 43 assortative mating 43 antigenic shift 43 genetic trait 43 genetic defect 43 PTPN# 43 Genetic predisposition 43 sub syndromal 43 schizoid personality 43 alleles 43 IGF1 43 classical scrapie 43 chromosomal rearrangements 43 fatal neurodegenerative 43 Empty nest 43 incurable neurodegenerative disease 43 deleterious mutations 43 OCA2 43 COMT gene 43 X chromosomes 43 APOE ε4 43 trypanosome 43 G#S mutation 43 mutations 43 LPA gene 43 Hashimoto thyroiditis 43 heterozygotes 43 antisocial tendencies 43 genetic predisposition 43 paternally inherited 43 inheritable 43 abnormal hemoglobin 42 mutant allele 42 parkinsonism 42 familial ALS 42 genes predisposing 42 heritable trait 42 C#BL/#J 42 MTHFR 42 MYH9 gene 42 disease epidermolysis bullosa 42 MECP2 gene 42 autosomes 42 haploid 42 Febrile seizures 42 Nicotine dependence 42 orthologous 42 genetically predetermined 42 reproductively isolated 42 Alu elements 42 zygotic 42 orthologous genes 42 MC4R gene 42 chromosome deletion 42 MLH1 42 genetic abnormalities 42 Mendelian inheritance 42 VHL gene 42 polyploid 42 C#Y 42 OPRM1 gene 42 unisexual 42 neurofibroma 42 IGF2 42 giant danio 42 monogenic 42 lissencephaly 42 mitochondrial mutations 42 APOE 42 D. melanogaster 42 Leber hereditary optic neuropathy 42 masculine traits 42 biological predisposition 42 coeval 42 WAGR syndrome 42 NF1 42 dysgenesis 42 SLC#A# [001] 42 Crouzon Syndrome 42 mutant genes 42 phenotypic variation 42 dopamine D4 receptor 42 outbred 42 lysosomal storage disease 41 Li Fraumeni syndrome 41 neuropsychiatric disorder 41 Atopic dermatitis 41 genomic imprinting 41 proband 41 beta thalassemia 41 imprinted genes 41 G allele 41 congenital disorders 41 Ehlers Danlos syndrome 41 Marfan syndrome connective tissue 41 antisense strand 41 HGPS 41 apolipoprotein E gene 41 hereditary hemochromatosis 41 gene mutation 41 Pax6 41 monozygotic twins 41 LMNA gene 41 Pervasive Developmental Disorder 41 rare chromosomal disorder 41 ciliated 41 cellular prion protein 41 combined immunodeficiency SCID 41 chromosomal rearrangement 41 chromatid 41 CFTR gene 41 neonatal respiratory distress 41 susceptibility genes 41 APOE gene 41 mutant alleles 41 epistasis 41 somatoform disorder 41 mtDNA mutations 41 fatal neuromuscular disorder 41 epigenetic 41 genetic disorder 41 segmental duplications 41 CHD7 41 frameshift mutation 41 inbred strains 41 pathological narcissism 41 meiotic recombination 41 characteristic 41 monophyletic 41 RCAN1 41 epigenetic modification 41 behavioral disinhibition 41 TP# mutation 41 beta globin 41 genetic 41 P. infestans 40 cystic fibrosis sickle cell 40 diploid 40 Arabidopsis plants 40 heterochromatin 40 Hurler syndrome 40 parkin gene 40 G#S [002] 40 allele 40 X inactivation 40 monozygotic 40 cerebellar 40 Heredity 40 epigenetic modifications 40 piRNAs 40 Alopecia areata 40 synuclein 40 Polycystic kidney disease 40 monomorphic 40 heritable traits 40 HLA gene 40 CYP#D# gene 40 Y chromosome 40 paralogs 40 tapeworm infection 40 centrosomes 40 genetic mutations 40 cerebellar hypoplasia 40 Pol IV 40 paraneoplastic 40 sporadic ALS 40 prairie vole 40 TACI mutations 40 Fig. 1C 40 APOE e4 40 genetic variant 40 melanocyte stem cells 40 S. cerevisiae 40 CYP#C# gene 40 A. thaliana 40 inherited neurological disorder 40 primary ciliary dyskinesia 40 aneuploid 40 proline rich 40 phenotypic expression 40 Treg cell 40 homozygote 40 multigenic 40 Polycystic ovary syndrome 40 FMR1 40 genetic recombination 40 Dental fluorosis 40 Seasonal affective disorder 40 myostatin gene 40 HLA molecules 40 Sandhoff disease 40 phthalate syndrome 40 metabolic abnormality 40 inherited genetic mutations 40 neurodevelopment disorder 40 archaeal 40 MLL gene 40 Vitamin B# deficiency 40 fig. S1 40 SGK1 40 neuritic 40 masculinizing 40 yellow tinge 40 genetic lineages 40 antisocial traits 40 presenilin 40 XY chromosome 40 ego dystonic 40 cyclicity 40 immunodeficiency 40 recessive genetic disorders 40 MC1R gene 40 neurasthenic 40 familial pancreatic cancer 40 Maroteaux Lamy Syndrome 40 epigenetic reprogramming 40 undiagnosed celiac disease 40 genetic alteration 40 Proteus syndrome 40 HYPP 39 observable traits 39 granulosa cell 39 Genetic variation 39 MAOA gene 39 masculinization 39 opsin 39 B. subtilis 39 involuntary tics 39 alternatively spliced 39 Apert 39 idiopathic 39 schizotypal 39 puerperal psychosis 39 Mendelian disorders 39 Rh incompatibility 39 evolvability 39 elongated limbs 39 Myotonic dystrophy 39 conformational 39 polyploids 39 dementia praecox 39 extra centrosomes 39 bilaterally symmetrical 39 allelic variation 39 dysmorphic 39 feminised 39 trisomy 39 Fanconi anemia 39 Congenital Adrenal Hyperplasia 39 dyskeratosis congenita 39 Wilhern 39 autosomal recessive genetic 39 epigenetic silencing 39 Aß# 39 thalassemia trait 39 hyperexcitability 39 biotype 39 ApoE gene 39 Cancerous cells 39 dimeric 39 SMN1 39 morphogen 39 #q#.# deletion syndrome 39 SRY gene 39 genetically 39 stochasticity 39 chromosomal instability 39 DRD4 gene 39 TP# gene 39 reproducing asexually 39 CNTNAP2 gene 39 clonal reproduction 39 myotonic dystrophy 39 spontaneous mutations 39 fig. S2 39 Lafora disease 39 neural crest cells 39 Supplementary Fig 39 DNA methylation patterns 39 aneuploidy 39 MHC genes 39 conspecifics 39 TCF#L# gene 39 neurodegenerative disorder 39 mouse ESCs 39 dizygotic twins 39 plausible hypothesis 39 hypoactive 39 APOE genotype 39 abnormal chromosomes 39 polydactyly 39 hemochromatosis 39 sawtooth pattern 39 Androgenetic alopecia 39 fibrous dysplasia 39 shorter lifespans 39 genetic susceptibility 39 Prefrontal 39 Asperger syndrome milder 39 haplogroup 39 hereditary disorder 39 autistic traits 39 mutational 39 D. simulans 39 susceptibility gene 39 S. sanguinis 39 chronicity 39 5 methylcytosine 39 chromosomal aberration 39 epiphenomenon 39 bdelloids 39 hyperactive impulsive 39 Agreeableness 39 systemic mastocytosis 39 homologs 39 fertilized egg splits 39 OCA2 gene 39 Quova delivers 39 CDH1 39 septo optic dysplasia 39 UGT#B# 39 DiGeorge syndrome 39 pea aphid 39 BARD1 39 sequence homology 39 Asperger disorder 39 meadow vole 39 Bacterial vaginosis 39 neuropsychological impairment 39 ploidy 39 dysthymic 39 Fig. 3B 39 chromosome #q# [001] 39 germline stem cells 39 apoE4 39 dyadic 39 retinal dysfunction 39 outbreeding 39 childhood disintegrative disorder 38 archetypally 38 vascular Ehlers Danlos 38 nonidentical 38 Alport syndrome 38 Abdominal obesity 38 PTEN mutations 38 prion protein gene 38 Meckel Gruber syndrome 38 unmethylated 38 germline 38 consanguineous 38 PON1 gene 38 GABRA2 gene 38 translocations 38 prokaryote 38 epigenetically 38 dizygotic 38 genes 38 Meckel Gruber 38 chromosomal aberrations 38 psychogenic 38 ENPP1 38 Worthingtons testified 38 GSTM1 gene 38 IKZF1 38 lysosomal storage diseases 38 ApoE4 38 SCA5 38 undesirable traits 38 progeria rare 38 genetic defects 38 breast cancer genes BRCA1 38 eusocial 38 Malignant mesothelioma 38 #q# [001] 38 velo cardio facial 38 CCR5 delta# 38 haplogroups 38 Rickettsia 38 heredity 38 Mendelian diseases 38 fossilization 38 genetically coded 38 Aunt Blanche 38 extraverted 38 chordate 38 Postpartum psychosis 38 Bardet Biedl Syndrome 38 chromosome #q#.# [001] 38 familial clustering 38 PRNP 38 Lesch Nyhan syndrome 38 C. neoformans 38 Y chromosomal 38 homeobox genes 38 neural crest 38 KCNQ1 38 neurological abnormalities 38 APOE4 gene 38 enzyme deficiency 38 hippocampal function 38 Fig. 3a 38 Jhdm2a 38 causally linked 38 euthymic patients 38 mammalian brains 38 androgen receptor gene 38 spontaneous remission 38 LRRK2 gene 38 Diamond Blackfan anemia 38 epidermolysis bullosa EB 38 histone modification 38 dimorphism 38 glycogen storage 38 predisposing factor 38 nurturant 38 Fig. 1b 38 epidermal cells 38 Leydig cells 38 centrosome 38 cone photoreceptors 38 alexia 38 Premature ejaculation 38 autoinflammatory diseases 38 Fragile X 38 chromosomal 38 #q#.# [001] 38 phenotypic variability 38 microcephalin 38 neurobiological disorder 38 Frontal lobe 38 domineering 38 stomatal 38 lateralized 38 gene 38 karyotype 38 huntingtin 38 HLA genes 38 chromosomal anomalies 38 ZNF# 38 MSH2 38 dopamine transporter gene 38 notochord 38 rhesus 38 Oppositional Defiant Disorder 38 homologous chromosomes 38 gene DRD4 38 Irritable bowel syndrome 38 virulence genes 38 comorbid disorders 38 mammary gland tumors 38 cis regulatory 38 CNTNAP2 38 stereotypically 38 Obsessive compulsive disorder 38 poorer prognosis 38 ARID1A 38 PrPSc 38 Dravet syndrome 38 HMGA2 gene 38 Or#b 38 roseola 38 chromosome 38 ApoE4 gene 38 A. gambiae 38 neuronal progenitor cells 38 melanocyte 38 mitochondrial DNA mutations 38 thymine 38 sporulation 38 parthenogenetic 38 Rb gene 38 patrilineal 38 Fig. 1a 38 epistatic 38 MLL2 38 invariant 38 haplotypes 38 familial aggregation 38 centrioles 38 microcephaly 38 unmodulated 38 Picky eating 38 progranulin 38 sexually reproducing 38 genetic alterations 38 evolutionarily conserved 38 paranoid schizoid 37 Drosophila melanogaster 37 Uveal melanoma 37 endosymbiosis 37 eccrine 37 genetically homogeneous 37 testis 37 eusociality 37 BRCA1 gene 37 cybrid 37 bimodal 37 autosomal dominant polycystic kidney 37 indistinctive 37 sRNAs 37 autoimmune thyroiditis 37 HLA identical 37 neurofibrillary 37 fungal genomes 37 offspring 37 clade B 37 deformational plagiocephaly 37 HNPCC 37 DRD4 37 lactase persistence 37 hermaphroditism 37 auditory neuropathy 37 histone methylation 37 recombination hotspots 37 R. equi 37 degenerative neurological disorder 37 apoE 37 CYP#E# gene 37 naturalistic worldview 37 myeloproliferative 37 Lamarckian 37 prion gene 37 hypercoagulable 37 Personality traits 37 mutated 37 mammary cancers 37 estrous cycle 37 nongenetic 37 androgen deficiency 37 nucleotide substitution 37 aetiological 37 tubule 37 Beckwith Wiedemann Syndrome 37 congenital disorder 37 var genes 37 male prairie voles 37 microdeletions 37 Prox1 37 Sickle cell 37 disulfide bond 37 Rh positive 37 gene deletions 37 VNTR 37 progranulin gene 37 ribosomal RNA 37 methylation patterns 37 Spinal muscular atrophy 37 granulomatous 37 Fig. 3b 37 incommunicative 37 BDNF gene 37 bimodal distribution 37 1 diabetes T1D 37 mitochondrial genes 37 genetically disposed 37 Y chromosomes 37 Neurofibromatosis type 37 hyperplastic 37 odorant receptor 37 Adam Pontipee 37 Penile cancer 37 CGG repeats 37 fungoides 37 alveolar rhabdomyosarcoma 37 premature ovarian 37 Muscular dystrophy 37 eukaryotic cell 37 causative genes 37 processive 37 genomic instability 37 unaffectionate 37 lymphoproliferative disorder 37 pronouncedly 37 F. graminearum 37 PTEN gene 37 Neuregulin 1 37 chromosome #q# [002] 37 hereditary nonpolyposis colorectal cancer 37 thalassemia sickle cell 37 achromatic 37 hypomanic episodes 37 Amborella 37 cytologically 37 heritable variation 37 MTHFR gene 37 reproductively 37 BRCA1 mutations 37 homocystinuria 37 genetic makeups 37 spinal muscle atrophy 37 probands 37 symptomatically 37 CYP#A# gene 37 debilitating neurodegenerative disorder 37 neurotic 37 brain malformation 37 progerin 37 chromosomally 37 trichomes 37 uniparental 37 Basal cell carcinoma 37 P. vivax 37 FOXP2 gene 37 apo E 37 δ 37 quiescent 37 Autistic Disorder 37 CALHM1 37 rs# [003] 37 sarcoid 37 dissociative disorders 37 incurable neurological disorder 37 Hox gene 37 masculinized 37 immunodominant 37 trait 37 pustular 37 DRD2 gene 37 frontotemporal dementia 37 constitutively active 37 uncharacterized 37 major histocompatibility complex 37 prodromal 37 pseudogenes 37 stathmin 37 predispose 37 prion strains 37 heterochromatic 37 unmarriageable 37 stereotypic 37 CAG repeats 37 outcrossing 37 fig. S4 37 AAT Deficiency 37 FTO gene 36 Pseudomonas syringae 36 cytochrome b 36 punctate 36 somatic mutation 36 sexual dimorphism 36 protein encoded 36 maladjustment 36 Follicular lymphoma 36 T rubrum 36 Ashkenazi Jewish 36 onset Alzheimer 36 human influenzas 36 Negroid 36 fig. 36 desmosomes 36 degenerative disorder 36 abnormal prion 36 cystic fibrosis Duchenne muscular 36 BRIP1 36 flightiness 36 Magnesium deficiency 36 untranslated regions 36 haplotype 36 charmingly naive 36 idiopathic epilepsy 36 DNA rearrangements 36 multinomial 36 heterozygosity 36 manipulativeness 36 codon 36 coexistent 36 ribosomal genes 36 affective psychosis 36 Von Willebrand disease 36 Plaque psoriasis 36 inbreeding 36 intergenic 36 tumor suppressor genes 36 evolutionary conserved 36 anaphylaxis angioedema 36 Fig. 1A 36 amnestic 36 genetically wired 36 CNVs 36 methylated 36 leucine zipper 36 Cystic fibrosis CF 36 Domesticated dogs 36 Tay Sachs thalassemia 36 radiosensitive 36 inborn traits 36 apelike 36 oscillatory behavior 36 gene variant 36 homologues 36 #p#.# [001] 36 MeCP2 gene 36 asexual 36 polyandrous 36 sociopathy 36 photoreceptor cell 36 modifier genes 36 T. vaginalis 36 diathesis 36 Plantar warts 36 gravitational perturbations 36 premorbid 36 Su var 36 Fig. 2a 36 pathological 36 Bifidobacteria 36 hereditary 36 sapiens 36 ductile deformation 36 distractible 36 #S rRNA genes 36 pathogenetic 36 chromosomal translocations 36 totipotent 36 LQTS 36 unloving 36 consanguineous marriages 36 DiGeorge Syndrome 36 genetically identical 36 subsyndromal 36 effeminacy 36 Chronic constipation 36 alpha synuclein gene 36 pelage 36 NR#A# gene 36 Kraepelin 36 hypochondriacal 36 phylogenetically 36 oncoproteins 36 inhibitory receptor 36 OCD obsessive compulsive disorder 36 metamorphism 36 Wolbachia strains 36 causative gene 36 noncoding 36 metazoan 36 noncoding regions 36 Synovial sarcoma 36 predisposing factors 36 angiosperms flowering plants 36 NF1 gene 36 genetic variability 36 CG methylation 36 M. leprae 36 telomeres shorten 36 clonal expansion 36 Pneumocystis carinii 36 dystonic 36 mycosis fungoides 36 masculinisation 36 grapheme color 36 Binge eating 36 TAp# 36 JAK2 mutation 36 mitochondrial DNA mtDNA 36 thyroiditis 36 Hypophosphatasia 36 Chromosomal 36 yellowish color 36 gene mutations 36 blackish brown 36 Strep throat 36 masculinised 36 Fig. 2C 36 non syndromic 36 steatohepatitis 36 ossify 36 myelitis 36 disabling neurological 36 Helicobacter 36 p# mutation 36 Pathological gambling 36 primordial germ cells 36 PGCs 36 PCNSL 36 Joubert syndrome 36 BRCA mutation 36 Retinitis pigmentosa 36 colouration 36 clonally 36 affiliative 36 prothrombotic 36 onsets 36 inherited neurodegenerative 36 spatio 36 ferroelectricity 36 progressive retinal degenerative 36 underlying pathophysiology 36 finely etched 36 histone H4 36 pseudogene 36 psychopathic traits 36 pathogenic mutations 36 maturational 36 Yeast infections 36 endogenous retrovirus 36 primitive neuroectodermal tumors 36 miRNA genes 36 Bos taurus 35 Heritability 35 Glioblastomas 35 eukaryote 35 primitive organisms 35 Krabbe leukodystrophy 35 evolutionarily speaking 35 rs# [002] 35 osteochondroma 35 CDKN2A 35 hyper IgE syndrome 35 chiari malformation 35 xanthus 35 aberrant 35 Allergic conjunctivitis 35 rDNA 35 globin 35 bivalent domains 35 predictible 35 chromosomal disorders 35 homochirality 35 Vpu 35 immunodeficiencies 35 permissive parenting 35 microsatellite instability 35 chromosomes 35 allelic 35 Oedipus complex 35 smectite 35 clades 35 macrocycle 35 highly pathogenic viruses 35 penile spines 35 paternal lineages 35 gait abnormalities 35 chromosomal abnormalities 35 generalized epilepsy 35 genetic rearrangements 35 dimorphic 35 cough syncope 35 monocots 35 Th2 responses 35 Mycoplasma species 35 superfetation 35 incompletely understood 35 fey 35 behavioral abnormalities 35 mutated BRCA1 35 assortative 35 phonic tics 35 linkage disequilibrium 35 chromosomal defects 35 muscular dystrophy cystic fibrosis 35 Mitochondrial 35 MHC molecules 35 DISC1 35 polyandry 35 anatomic abnormalities 35 Fig. 1B 35 nonprogressive 35 APOC3 35 gut microbes 35 Oedipal complex 35 oncogene addiction 35 enzymatic activity 35 deeply ingrained maladaptive 35 mtDNA 35 guanine 35 #q# deletion 35 lactase gene 35 oncogenic transformation 35 rRNA 35 Chalcopyrite 35 polymicrobial 35 PCR amplified 35 Fig. 3C 35 gene duplications 35 pleiotropy 35 infiltrative 35 agnosia 35 TGFBR1 35 mutable 35 musth 35 Agrobacterium tumefaciens 35 Lady Marchmain 35 epigenetic inheritance 35 DICER1 35 hairlessness 35 abnormal 35 inherited 35 heritability 35 S. pombe 35 estrogenic effects 35 retrovirus 35 pathognomonic 35 Neuroticism 35 Drosophila 35 unicellular 35 Bacteroides 35 gonadal 35 human leukocyte antigen 35 nonidentical twins 35 5 hydroxymethylcytosine 35 ontogeny 35 Powdery mildew 35 bilaterians 35 morphologic 35 inexpressive 35 epigenetic changes 35 Haplogroup 35 biochemical imbalances 35 p# mutations 35 mammalian evolution 35 suppressor gene