Related by context. All words. (Click for frequent words.) 63 mutated K ras 59 gene predisposing 59 TP# mutation 58 Rh factor 58 APOL1 57 BRIP1 57 cardiac channelopathies 57 HLA markers 57 monozygotic twin 57 impair fertility 57 genes predisposing 57 spontaneous miscarriages 57 CHEK2 57 FGFR2 gene 57 gene BRCA2 57 synthetic lethality 57 BRCA1 mutations 56 BARD1 56 epigenetic changes 56 HLA DQ2 56 Fragile X gene 56 APOE ε4 56 embryo biopsy 56 APOE genotype 56 NF1 gene 55 aneuploidy screening 55 apolipoprotein E gene 55 STK# gene 55 mutated BRCA 55 hereditary predisposition 55 pre eclamptic 55 prion gene 55 precancerous condition 55 causative mutation 55 Ets2 55 genomewide 55 APOE e4 55 transgenic rats 55 egg retrieval 54 #q# deletion 54 woman ovulates 54 Entamoeba 54 MC4R gene 54 thyroid deficiency 54 progranulin gene 54 MYH9 gene 54 BRCA1 mutation 54 chromosomal aberrations 54 ovulatory cycles 54 CFTR gene mutations 54 clefting 54 NR#A# gene 54 transfusion syndrome 54 TMPRSS2 ERG fusion 54 maternally derived 54 ABCB1 gene 54 inherited mutations 54 Genetic variants 54 maternally inherited 54 chromosome translocations 54 CHD7 54 CYP#D# gene 54 gastric carcinomas 54 BRCA mutation carriers 54 BRCA mutation 54 PALB2 54 ovariectomy 54 breast cancer genes BRCA1 54 promoter hypermethylation 53 potent inducer 53 monogenic 53 Heavy menstrual bleeding 53 BRCA mutations 53 phenotypic expression 53 reproductive endocrine 53 aneuploid 53 laforin 53 placental malaria 53 mitochondrial mutations 53 Li Fraumeni 53 BRCA2 gene 53 teratogens 53 hypermethylated 53 BRCA1 gene 53 preimplantation 53 germline mutations 53 chromosomal alterations 53 TCF#L# gene 53 chlamydial infection 53 recessive genetic 53 histocompatibility 53 PALB2 gene 53 Genetic variation 53 LRRK2 gene 53 genetic loci 53 testicular biopsy 53 monozygotic twins 53 endometrial cancers 53 MC1R gene 53 TOMM# 53 spontaneous mutations 53 iPS derived 52 malarial parasites 52 gene amplification 52 fruitfly Drosophila 52 chromosomal anomalies 52 testicular germ cell 52 abnormal Pap smear 52 Levy Lahad 52 epigenetic markers 52 egg follicles 52 gestational diabetes mellitus 52 MSH2 52 p# mutations 52 molar pregnancy 52 mutant allele 52 mosaicism 52 K ras gene 52 preeclamptic 52 causative genes 52 thyroid nodules 52 modifier genes 52 MEF2A 52 recessive trait 52 HLA DRB1 52 familial hypercholesterolaemia FH 52 PTEN gene 52 M. genitalium 52 SOD2 gene 52 confers susceptibility 52 UGT#B# 52 androgen receptor gene 52 microdeletion 52 embyros 52 familial adenomatous polyposis 52 genetic manipulations 52 HLA G 52 de novo mutations 52 mitochondrial DNA mtDNA 52 IDH2 52 genetic locus 52 chromosomal deletions 51 herpesviruses 51 operable breast cancer 51 RhD negative 51 Li Fraumeni syndrome 51 chromosomal defects 51 aneuploidies 51 heterozygote 51 ApoE gene 51 multigenic 51 uterus womb 51 familial ALS 51 salivary proteins 51 recessive mutations 51 FUS protein 51 PrPSc 51 mammary cells 51 fetal malformations 51 inheritable diseases 51 chemosensitivity 51 primordial germ cells 51 genetic syndromes 51 CFTR gene 51 methylation markers 51 mutated genes 51 genetic polymorphisms 51 APOE4 51 paternally inherited 51 somatic mutation 51 paratuberculosis 51 mammary cancers 51 sickle cell hemoglobin 51 HbF 51 Kufs disease 51 epigenetic inheritance 51 ALK gene 51 mammary stem cells 51 somatic mutations 51 genetic polymorphism 51 chromosome rearrangements 51 ductal breast cancer 51 genomic alterations 51 TGFBR1 * 6A 51 Genetic predisposition 51 NEIL1 51 precancerous tumors 51 female hormone progesterone 51 human leukocyte antigens 51 MTHFR 51 LRAT 51 microdeletions 51 metabolizing enzymes 51 Helicobacter 51 Genetic variations 51 Klinefelter syndrome 51 multigene 51 familial pancreatic cancer 51 Rb gene 51 CYP#C# [002] 51 observable traits 51 ApoE4 gene 50 orchitis 50 recessive mutation 50 Leydig cells 50 nongenetic 50 hereditary breast cancer 50 peroxisome 50 pancreatic tissue 50 gamma globin gene 50 MTHFR gene 50 environmental toxicants 50 anal lesions 50 underlying pathophysiology 50 Genetic mutations 50 NPM1 gene 50 HFE gene 50 missense mutations 50 maternally transmitted 50 dopamine transporter gene 50 chromosomal anomaly 50 amyloid toxicity 50 genetic alteration 50 GFP gene 50 genetic makeups 50 molecular abnormalities 50 ovarian dysfunction 50 mtDNA mutations 50 endometrial hyperplasia 50 vitro maturation 50 genetically mapped 50 developmental neurotoxicity 50 GSTT1 50 molecular determinants 50 parkin gene 50 #S rDNA 50 Pre implantation genetic 50 immunodeficient 50 Meckel Gruber 50 congenital disorders 50 T. vaginalis 50 virulence genes 50 prenatally diagnosed 50 MC1R 50 bacterial symbionts 50 abnormal pap smears 50 mutant genes 50 oocyte retrieval 50 gene rearrangements 50 mitochondrial DNA mutations 50 SMN2 gene 50 abnormal chromosomes 50 immune suppressing 50 DNA methylation patterns 50 FGFs 50 CDH1 50 oophorectomy 50 Rhesus D 50 VHL gene 50 recurrent miscarriages 50 ADPKD 50 phthalate syndrome 50 recurrent ovarian 50 Aneuploidy 50 number variations CNVs 50 axonal degeneration 50 abnormal Pap test 50 BRCA gene 50 abnormal prions 50 spontaneous mutation 50 prophylactic mastectomies 50 stimulate neurogenesis 50 precancerous cervical 50 causative gene 50 Cryptococcus neoformans 49 tissue homeostasis 49 LIS1 49 tumor subtype 49 PTPN# 49 genetic variants associated 49 TRIM5a 49 secrete proteins 49 subfertile 49 dysfunctional voiding 49 ovarian hyperstimulation 49 familial clustering 49 hypothalamic amenorrhea 49 LRP5 49 undergone hysterectomy 49 Retrograde ejaculation 49 genetic recombination 49 penetrance 49 proband 49 gene mutations 49 inherited predisposition 49 genetically attenuated 49 methylation patterns 49 preventive mastectomies 49 immunologically compatible 49 heritable genetic 49 Dr. Victor Velculescu 49 nucleus Chinnery 49 splice junctions 49 CCL#L# 49 post natally 49 epigenetic mechanisms 49 Spinal muscular atrophy 49 mutagens 49 singleton pregnancy 49 fertilized ova 49 chromosomal disorders 49 genetic mutations 49 genetic abnormalities 49 BRCA2 gene mutations 49 STAT4 49 MAPCs 49 PPCM 49 aberrant methylation 49 sCJD 49 Amniocentesis 49 outer membrane proteins 49 neuroligins 49 Deoxyribonucleic acid DNA 49 Mutant mice 49 Mycoplasma genitalium 49 exome sequencing 49 protein isoforms 49 HLA molecules 49 transplanted ovarian 49 parasitic nematode 49 tumorigenicity 49 prodynorphin 49 stimulate ovulation 49 mutant worms 49 Rh positive 49 alpha synuclein gene 49 aneuploid cells 49 mutations 49 HLA identical 49 diploid cells 49 MIF protein 49 germline mutation 49 differential gene expression 49 HOX genes 49 Sox9 49 anovulatory 49 JAK mutations 49 detect precancerous 49 recurrent miscarriage 49 noncancerous growths 49 induce ovulation 49 Neanderthal genes 49 T. cruzi 49 pathogenic mutations 49 hemoglobins 49 achromatopsia 49 astrocyte cells 49 genomewide association studies 49 HNPCC 49 Apobec3 49 spontaneously aborted 49 HLA genes 49 genotoxic stress 49 LPA gene 49 MYH9 48 SRY gene 48 PARP inhibition 48 warfarin dosing 48 abruption 48 Yamanaka recipe 48 Fallopian tube 48 cancerous polyp 48 mitochondrial metabolism 48 human chorionic gonadotrophin hCG 48 prion infection 48 Brugada Syndrome 48 uterine tumors 48 cell nuclei 48 bilateral oophorectomy 48 epigenetically 48 gamete 48 KIBRA 48 polycystic ovarian syndrome PCOS 48 Stress hormones 48 genomic biomarkers 48 xenobiotic 48 MIF gene 48 Single Nucleotide Polymorphisms SNPs 48 GABRA2 48 reproductive abnormalities 48 dominantly inherited 48 P. patens 48 TMEM#B 48 epigenetic regulation 48 bile acid metabolism 48 LQTS 48 myostatin gene 48 Sertoli cells 48 non coding RNA 48 toxoplasma 48 Ionizing radiation 48 autosomal dominant inheritance 48 ultra rapid metabolizer 48 coding exons 48 tumor suppressor protein 48 gene loci 48 humanized mouse 48 suppressor gene 48 FGFR2 48 gene locus 48 G#S mutation 48 IUD inserted 48 gene deletions 48 Trichomonas 48 undergoing fertility treatments 48 Folate deficiency 48 reproductive tracts 48 periodontal tissues 48 BRCA genes 48 ribosomal genes 48 genetic susceptibility 48 metabolic enzymes 48 generalized vitiligo 48 RhD 48 genes BRCA1 48 prophylactic mastectomy 48 HLA DQ 48 Toxoplasma gondii 48 trichomonas 48 infertility miscarriages 48 metabolomic profile 48 palladin 48 ultrastructure 48 malaria parasite Plasmodium falciparum 48 malaria parasite genome 48 HLAs 48 mitochondrial proteins 48 fetal microchimerism 48 hereditary disorders 48 HHV 6 48 preimplantation genetic diagnosis PGD 48 modulate gene expression 48 mycobacterial 48 blastomeres 48 genomic imprinting 48 mutation 48 genetic determinants 48 nulliparous 48 genetic rearrangements 48 gene variation 48 SERT gene 48 lentiviruses 48 chromosomal translocations 48 vitro maturation IVM 48 BCL#A 48 PTEN mutations 48 SOD1 gene 48 polycystic ovary syndrome PCOS 48 dizygotic twins 48 SNPs pronounced snips 48 Malaria parasite 48 metazoans 48 genomic rearrangements 48 HMGCR 48 LRRK2 mutations 48 herpes viruses 48 beta globin gene 48 epigenetic silencing 48 mammary gland tumors 48 immunological mechanisms 48 IUGR 48 malaria endemic regions 48 chimerism 48 pea aphid 48 epistasis 48 nonpathogenic 48 secondary amenorrhea 48 microbiomes 48 biologic pathways 48 chromosome aberrations 48 muscular dystrophy cystic fibrosis 48 von Hippel Lindau 48 cultured neurons 48 pilocytic astrocytomas 47 dopamine receptor gene 47 causative mutations 47 infectious prion proteins 47 orchidectomy 47 epigenetic modifications 47 inherit predisposition 47 C EBP alpha 47 neuroglobin 47 rickettsial 47 chorionic villus sampling 47 FOXP2 gene 47 RNA ribonucleic acid 47 PCA3 gene 47 TP# gene 47 DNA rearrangements 47 Froguel 47 Rh incompatibility 47 Aspergillus nidulans 47 protein coding RNAs 47 drugable 47 KCNQ1 47 MHC genes 47 germline 47 abnormal cervical 47 epigenetic alterations 47 Tr DNA 47 mitochondrial disorders 47 FTO variant 47 genetic abnormality 47 genes CYP#C# 47 SLC#A# gene [001] 47 MeCP2 protein 47 colostomies 47 vesicular stomatitis virus 47 rhesus negative 47 exomes 47 vasopressin receptor 47 HLA alleles 47 DNA deoxyribonucleic acid 47 allelic variation 47 chromatin proteins 47 UGT#A# 47 INF2 47 ductal lavage 47 glucocorticoid receptors 47 apoE4 47 heritable diseases 47 IL#R 47 morally licit 47 premenstrual syndrome PMS 47 transcriptomic 47 muscular dystrophies 47 mammalian embryos 47 susceptibility gene 47 tubal pregnancy 47 A. fumigatus 47 vaginal fluids 47 proteomic analyzes 47 physiological characteristics 47 Fc gamma receptor 47 Jhdm2a 47 IKZF1 47 gene expression patterns 47 Foxp2 47 T. gondii 47 genetically predetermined 47 galactosemia 47 apoE 47 genetic alterations 47 mutated protein 47 chromosomal abnormalities 47 chromosome #q# [001] 47 Notch receptor 47 GAB2 47 chromosomal aberration 47 S nitrosylation 47 STK# [002] 47 consanguineous marriage 47 GBS colonization 47 transplanting organs 47 telomere DNA 47 abort fetus 47 allelic 47 JAK2 mutation 47 KIAA# 47 genital tracts 47 microsatellite instability 47 HMGA2 47 bacterial genomes 47 sphingolipid 47 ZNF# 47 metabolize cholesterol 47 homozygote 47 hippocampal function 47 bacterial virulence 47 Evolutionarily speaking 47 microchimerism 47 klotho gene 47 inheritable genetic 47 #p#.# [002] 47 irregular menstrual cycle 47 heritable traits 47 estrogen metabolism 47 Preimplantation Factor 47 toxicologic 47 pharmacodynamic markers 47 epigenetic modification 47 fetal chromosomal abnormalities 47 genetic modifiers 47 genes BRCA 47 hypermethylation 47 thale cress Arabidopsis thaliana 47 BChE 47 Genotypic 47 transcriptome profiling 47 genomic profiling 47 autism susceptibility genes 47 airborne fungal spores 47 CTVT 47 breast cancer metastasis 47 C. difficile toxins 47 unexplained infertility 47 enzymatically active 47 bioengineered mice 47 Apert syndrome 47 Mendelian 47 monozygotic 47 APOE gene 46 proteomes 46 primordial follicles 46 synaptogenesis 46 immature dendritic cells 46 number variation CNV 46 effector molecules 46 vertebrate embryos 46 testosterone supplementation 46 sporadic ALS 46 methylated DNA 46 unexplained stillbirth 46 previously undescribed 46 pre cancerous growths 46 MLL2 46 chromosomal instability 46 peroxisomes 46 fungal genomes 46 Pseudomonas syringae 46 M. pneumoniae 46 undergoing hysterectomy 46 telomeres shorten 46 paternal lineage 46 mature oocytes 46 miRNA expression 46 susceptibility locus 46 undergoing bariatric surgery 46 Hair follicles 46 TACI mutations 46 COMT gene 46 #p#.# [001] 46 euthyroid 46 ovulation inducing 46 underactive thyroids 46 chromosomally abnormal 46 metabonomics 46 antimetastatic 46 Genetic testing 46 PCR RFLP 46 neoplastic 46 effector protein 46 biosynthetic pathways 46 rhinovirus infection 46 CYP#C# [001] 46 postnatally 46 ovarian transplant 46 epiblast stem cells 46 transcriptomics 46 SORL1 gene 46 evolvability 46 Dr Taranissi 46 FMR1 gene 46 Arabidopsis genes 46 microcephalin 46 single celled yeast 46 parasite Toxoplasma gondii 46 Plasmodium parasites 46 ADRB2 46 Klotho gene 46 cAMP signaling 46 IGF2 46 MECP2 gene 46 congenital CMV infection 46 obligate intracellular 46 Prevotella 46 maternal lineage 46 intracellular compartments 46 transcriptomes 46 genetic 46 shorten telomeres 46 Velculescu 46 genetic imprinting 46 haploid 46 chromosomal regions 46 Xenopus embryos 46 Chlamydia infection 46 homozygosity 46 radioiodine therapy 46 semen saliva 46 orthologs 46 HSF1 46 CYP#E# gene 46 chloroplast genome 46 heritable disorders 46 giant danio 46 enterotypes 46 MCAD deficiency 46 Cryptococcus 46 inherited genetic mutation 46 sirtuin enzymes 46 epigenetic marks 46 HLA B# 46 chromosomally normal 46 gestational hypertension 46 IDH1 mutations 46 NOD2 46 fascin 46 evolutionarily distant 46 implantation genetic 46 prion strains 46 chloroplast DNA 46 infantile hemangiomas 46 antisense therapies 46 genetically altered mouse 46 herpes virus infection 46 nucleotide substitutions 46 dedifferentiation 46 VKORC1 46 antisense RNA 46 anencephalic 46 Folic acid supplements 46 Math1 46 Wolbachia strains 46 recessive genes 46 NPY gene 46 genetic aberrations 46 organogenesis 46 morphological traits 46 nematode worm C. elegans 46 C. neoformans 46 MLH1 46 metabolome 46 mutant alleles 46 metabolomic profiling 46 premature ovarian 46 nonfunctioning kidneys 46 sexually reproducing 46 cephalic presentation 46 inherited maternally 46 HPRT gene 46 FGF signaling 46 allele frequencies 46 embryo clones 46 breech births 46 Sanger sequencing 46 glycolipid 46 Hirschsprung 46 imprinted genes 46 budding yeast 46 HMMR 46 Malignant tumors 46 Fetal distress 46 polycystic ovaries 46 Wnt proteins 46 FMRP protein 46 initiates cascade 46 HIV seropositive 46 nanocarrier 46 mutated gene 46 transcriptional regulation 46 mitochondrial genomes 46 inbred strains 46 parthenogenic 46 mitochondrial gene 46 genetically defective 46 microglial 46 TCF4 46 autosomal 46 furiosus 46 genes encoding 46 familial predisposition 46 human leukocyte antigen 46 therapeutically useful 46 genomic variants 46 post partum haemorrhage 46 babies umbilical cords 45 Dr. Rafii 45 GATA4 45 Smac mimic 45 SMN2 45 hematopoetic stem cells 45 neural crest 45 DRD4 45 DNA Deoxyribonucleic Acid 45 pleiotropic 45 apoptosis pathway 45 Follicle Stimulating Hormone 45 amniotic cells 45 anal warts 45 uncircumcised males 45 premature menopause 45 primary cilia 45 antenatal depression 45 abnormal Pap 45 prostate glands 45 lincRNA 45 CB2 receptor 45 Ovary removal 45 pharmacogenetic 45 commensal bacteria 45 microbial flora 45 orchiectomy 45 replicative 45 irregular menstrual cycles 45 Plasmodium parasite 45 trimester ultrasound 45 sequence homology 45 Simian Immunodeficiency Virus 45 Male infertility 45 enucleated 45 genetic markers 45 drug clomiphene 45 phenotypic variability 45 intracytoplasmic sperm injection 45 mRNA transcripts 45 uterine scar 45 inhibit ovulation 45 tubal 45 sister chromatid 45 SMN1 gene 45 baker yeast Saccharomyces cerevisiae 45 precancerous spots 45 drank pomegranate juice 45 IRS1 45 chromosome abnormalities 45 Fanconi anemia 45 germline cells 45 IDH mutations 45 hormone FSH 45 DRD2 gene 45 protein phosphorylation 45 endospores 45 SH2 B 45 IDH1 45 mtDNA sequences 45 MCADD 45 endogenous retroviruses 45 cryo preserved 45 gene variant 45 phylogenetic analyzes 45 GPx 45 IVF embryo 45 bacterial vaginosis 45 genotypic 45 transdifferentiation 45 genetic variants 45 demethylating 45 prolapsed uterus 45 neural cells 45 H#Y 45 cybrid 45 CFH gene 45 diseased liver 45 curable cancers 45 Folic acid deficiency 45 gene expression microarray 45 warfarin dose 45 hormone aldosterone 45 Leishmania parasites 45 asymptomatic hypothyroidism 45 susceptibility genes 45 RISUG 45 retrovirus 45 gene mutation 45 congenital abnormalities 45 ribosomal RNA 45 ovary stimulating 45 pattern baldness 45 polyploid 45 cDNA microarray 45 heterozygosity 45 nematode worms 45 deacetylation 45 EBV infection 45 polygenic 45 abnormal hemoglobin 45 DLX5 45 validate biomarkers 45 diagnosed prenatally 45 SETDB1 45 gynecological examination 45 varicocele 45 ionizing irradiation 45 genetic variant 45 clostridia 45 CYP#C# gene 45 bacterial flora 45 ARID1A 45 Ashwell receptor 45 undiagnosed celiac disease 45 oncomodulin 45 gene duplications 45 Borrelia 45 Wnt#b 45 preimplantation genetic 45 genetically inherited 45 blastomere 45 antibiotic resistant genes 45 #S rRNA gene 45 RNA splicing 45 aryl hydrocarbon receptor 45 cypin 45 LMNA 45 S. pombe 45 implanted embryos 45 hormonal stimulation 45 Preimplantation genetic diagnosis 45 fetal abnormalities 45 induced pluripotent cells 45 GBM tumors 45 gamete donors 45 divide asymmetrically 45 FMR1 45 Posiphen TM 45 molecular mimicry 45 folic acid supplement 45 ovaries removed 45 MLL gene 45 fertilising eggs 44 cybrids 44 Leptospira 44 LJ# [002] 44 suppress ovulation 44 chemistry microbiology immunology 44 autologous transplant 44 abort fetuses 44 telomere lengths 44 underlying molecular mechanisms 44 cancerous breast 44 overt hypothyroidism 44 epigenomic 44 ovarian follicles 44 micro RNAs 44 varicoceles 44 retroviral 44 Telomere length 44 RNA silencing 44 gene variants 44 chromosomal imbalance 44 Bt toxins 44 mitochondrial DNA sequence 44 genetically susceptible 44 gene expression microarrays 44 mutated EGFR 44 uncurable 44 Menkes disease 44 epigenomes 44 defective mitochondria 44 filoviruses 44 KRAS gene 44 HPV# 44 genotype phenotype 44 karyotype 44 pea aphids 44 Hirschsprung disease 44 primary ovarian insufficiency 44 totipotent 44 mRNA molecules 44 PGD PGS 44 Drosophila genome 44 Contraceptive pill 44 stillborn infants 44 histone modifications 44 PCOD 44 genetic susceptibilities 44 IL 7R 44 ovarian stimulation 44 HLA B# gene 44 invitro 44 BRCA1 44 heritable 44 Hsp# [001] 44 glycan microarray 44 Mycobacterium smegmatis 44 aneuploidy 44 Thermus thermophilus 44 incurable genetic 44 fertilized ovum 44 molecular underpinnings 44 lactose tolerance 44 inbreeding depression 44 Dr. Vitetta 44 genome decoded 44 lincRNAs 44 chromatin structure 44 frequent ejaculation 44 ovarian hyperstimulation syndrome 44 Nicotiana benthamiana 44 ovarian tumors 44 Notch receptors 44 insertional mutagenesis 44 evolutionary relatedness 44 bdelloid rotifer 44 limbed vertebrates 44 viral genomes 44 HELLP syndrome 44 diethylstilbestrol 44 pathogenic mechanisms