| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | J F Crow | |
| P2860 | cites work | Sex differences in mutation rate in higher primates estimated from AMG intron sequences | Q48052208 |
| Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients. | Q50990244 | ||
| A study of parental age effects on the occurrence of fresh mutations for the Apert syndrome. | Q53717616 | ||
| A paternal wash in Apert syndrome | Q56383962 | ||
| Parental age at conception and offspring longevity | Q57730472 | ||
| Spontaneous mutation in man | Q67508556 | ||
| Selection against harmful mutations in large sexual and asexual populations | Q70563103 | ||
| Mutation frequency in human blood cells increases with age | Q71758731 | ||
| The mutation rate of the gene for haemophilia, and its segregation ratios in males and females | Q83229412 | ||
| The gene | Q83314169 | ||
| Paternal age and the risk of congenital heart defects | Q22337382 | ||
| Parent-of-origin effects in multiple endocrine neoplasia type 2B | Q24672503 | ||
| Spontaneous mutation and parental age in humans | Q24676048 | ||
| Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine | Q24680144 | ||
| Efficiency of truncation selection | Q28305670 | ||
| High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders | Q30502821 | ||
| On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis | Q33673489 | ||
| The effects of spontaneous mutation on quantitative traits. I. Variances and covariances of life history traits | Q33963892 | ||
| Comparing mutational variabilities. | Q33968050 | ||
| THE GENETIC STRUCTURE OF NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER. I. SPONTANEOUS MUTATION RATE OF POLYGENES CONTROLLING VIABILITY | Q33981138 | ||
| Homozygous viability and fertility loads in Drosophila melanogaster | Q33982737 | ||
| The mutational load with epistatic gene interactions in fitness | Q33983691 | ||
| Mutation rate and dominance of genes affecting viability in Drosophila melanogaster | Q33988415 | ||
| Spontaneous and ethyl methanesulfonate-induced mutations controlling viability in Drosophila melanogaster. II. Homozygous effect of polygenic mutations | Q33992507 | ||
| Selection differentials and selection coefficients | Q33992736 | ||
| How much do we know about spontaneous human mutation rates? | Q34061777 | ||
| Contamination of the genome by very slightly deleterious mutations: why have we not died 100 times over? | Q34288465 | ||
| Our load of mutations | Q34295607 | ||
| Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia | Q34322623 | ||
| Trinucleotide repeat length instability and age of onset in Huntington's disease | Q34357407 | ||
| Exclusive paternal origin of new mutations in Apert syndrome | Q34385938 | ||
| The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease | Q34532438 | ||
| Frequency and nature of specific-locus mutations induced in female mice by radiations and chemicals: a review | Q35148417 | ||
| Mutation in human populations | Q39494010 | ||
| Spontaneous mutation as a risk factor | Q40930713 | ||
| Human aneuploidy: incidence, origin, and etiology | Q41202582 | ||
| Nature of deleterious mutation load in Drosophila. | Q42967314 | ||
| Factor VIII gene inversions in severe hemophilia A: results of an international consortium study. | Q45868290 | ||
| P433 | issue | 16 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 8380-6 | |
| P577 | publication date | 1997-08-05 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | The high spontaneous mutation rate: is it a health risk? | |
| P478 | volume | 94 |
| Q73895737 | A comparative study of ejaculate traits in three endangered ungulates with different levels of inbreeding: fluctuating asymmetry as an indicator of reproductive and genetic stress |
| Q52041272 | A comprehensive model of mutations affecting fitness and inferences for Arabidopsis thaliana. |
| Q92620768 | A little bit of sex prevents mutation accumulation even in apomictic polyploid plants |
| Q46615460 | A multigenerational effect of parental age on offspring size but not fitness in common duckweed (Lemna minor). |
| Q73259086 | A new study challenges the current belief of a high human male:female mutation ratio |
| Q41053593 | Advanced Paternal Age and Risk of Musculoskeletal Congenital Anomalies in Offspring |
| Q34599167 | Advanced parental age and the risk of autism spectrum disorder |
| Q41264159 | Advanced paternal age and parental history of schizophrenia |
| Q22337254 | Advanced paternal age and reproductive outcome |
| Q50344675 | Advancing paternal age and simplex autism |
| Q57414261 | Age at first birth in women is genetically associated with increased risk of schizophrenia |
| Q33582225 | Age- and temperature-dependent somatic mutation accumulation in Drosophila melanogaster |
| Q47652949 | Are children of older fathers at risk for genetic disorders? |
| Q34283911 | Base excision repair in a network of defence and tolerance |
| Q34276065 | Base excision repair is limited by different proteins in male germ cell nuclear extracts prepared from young and old mice |
| Q24619872 | Biodemography of exceptional longevity: early-life and mid-life predictors of human longevity |
| Q28748265 | Biological species is the only possible form of existence for higher organisms: the evolutionary meaning of sexual reproduction |
| Q50302247 | Brief Report: Phenotypic Differences and their Relationship to Paternal Age and Gender in Autism Spectrum Disorder |
| Q34665596 | Brief report: parental age and the sex ratio in autism |
| Q51775095 | Characteristics, causes and evolutionary consequences of male-biased mutation. |
| Q59212648 | Characterization of unstable microsatellites in mice: No evidence for germline mutation induction following gamma-radiation exposure |
| Q47912883 | DNA helix: the importance of being AT-rich. |
| Q35664448 | DNA polymerase beta is critical for genomic stability of sperm cells |
| Q36268064 | DNA repair pathway choice is influenced by the health of Drosophila melanogaster |
| Q34388868 | DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation rates |
| Q34133424 | Delayed child-bearing |
| Q47864795 | Delayed maternity and risk at delivery |
| Q35113063 | Deleterious genomic mutation rate for viability in Drosophila melanogaster using concomitant sibling controls |
| Q43578518 | Direct separation of in vivo and in vitro am3 revertants in transgenic mice carrying the phiX174 am3, cs70 vector |
| Q37050787 | Do heat stress and deficits in DNA repair pathways have a negative impact on male fertility? |
| Q35933888 | Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases |
| Q34602537 | EMS-induced polygenic mutation rates for nine quantitative characters in Drosophila melanogaster |
| Q35990909 | Early-Life Factors and Risk of Parkinson's Disease: A Register-Based Cohort Study |
| Q79733597 | Effectiveness of sexual selection in preventing fitness deterioration in bulb mite populations under relaxed natural selection |
| Q33933796 | Effects of chemical contaminants on genetic diversity in natural populations: implications for biomonitoring and ecotoxicology |
| Q28267889 | Effects of familial risk factors and place of birth on the risk of autism: a nationwide register-based study |
| Q43416279 | Elderly persons with elderly fathers - do they face additional risks? |
| Q34454629 | Environmental dependence of inbreeding depression in cultured Coho salmon (Oncorhynchus kisutch): aggressiveness, dominance and intraspecific competition. |
| Q34646160 | Environmental stress and mutational load in diploid strains of the yeast Saccharomyces cerevisiae |
| Q24604149 | Error-prone bypass of certain DNA lesions by the human DNA polymerase kappa |
| Q24548130 | Estimate of the mutation rate per nucleotide in humans |
| Q24804367 | Evidence for widespread degradation of gene control regions in hominid genomes |
| Q33633422 | Evidence that replication-associated mutation alone does not explain between-chromosome differences in substitution rates |
| Q33300344 | Evolution of female preference for younger males |
| Q55058456 | Facial fluctuating asymmetry is not associated with childhood ill-health in a large British cohort study. |
| Q35647831 | Fitness Consequences of Advanced Ancestral Age over Three Generations in Humans |
| Q54070830 | GENETIC LOAD OF THE YEAST SACCHAROMYCES CEREVISIAE UNDER DIVERSE ENVIRONMENTAL CONDITIONS. |
| Q39632462 | Genealogical process on a correlated fitness landscape |
| Q74258800 | Genetic engineering: what are we fearing? |
| Q33949730 | Genetic screening in patients of reproductive age. How do you advise prospective parents who want to know specific risks? |
| Q50305587 | Genetics: The rate of human mutation |
| Q40989489 | Germline Stem Cell Competition, Mutation Hot Spots, Genetic Disorders, and Older Fathers |
| Q89628360 | Haldane and modern evolutionary genetics |
| Q24548061 | Hardy, Weinberg and language impediments |
| Q73606389 | Heterogeneous mutation processes in human microsatellite DNA sequences |
| Q34491535 | High genomic deleterious mutation rates in hominids |
| Q52922431 | How important is DNA replication for mutagenesis? |
| Q35213745 | Human nutrition and food research: opportunities and challenges in the post-genomic era |
| Q48205348 | Identification and characterization of a novel splice variant of mouse and rat cytochrome b5/cytochrome b5 reductase. |
| Q33394214 | Impact of inbreeding on fertility in a pre-industrial population |
| Q34034696 | Implications of advancing paternal age: does it affect offspring school performance? |
| Q36320029 | Implications of fidelity difference between the leading and the lagging strand of DNA for the acceleration of evolution |
| Q38952645 | In Genes We Trust: Germline Engineering, Eugenics, and the Future of the Human Genome |
| Q33319616 | Increased transmission of mutations by low-condition females: evidence for condition-dependent DNA repair |
| Q36962345 | Investigating the specific core genetic-and-epigenetic networks of cellular mechanisms involved in human aging in peripheral blood mononuclear cells |
| Q39754055 | Invited commentary: taking the search for causes of schizophrenia to a different level |
| Q77525543 | Ionizing radiation and genetic risks IX. Estimates of the frequencies of mendelian diseases and spontaneous mutation rates in human populations: a 1998 perspective |
| Q30616268 | Ionizing radiation and genetic risks. XI. The doubling dose estimates from the mid-1950s to the present and the conceptual change to the use of human data on spontaneous mutation rates and mouse data on induced mutation rates for doubling dose calcu |
| Q34617609 | Is the rate of insertion and deletion mutation male biased?: Molecular evolutionary analysis of avian and primate sex chromosome sequences. |
| Q83229123 | Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation |
| Q43569689 | Late paternity and stillbirth risk |
| Q43891060 | Lineage-specific variation in slow- and fast-X evolution in primates. |
| Q57133292 | Lineages evolved under stronger sexual selection show superior ability to invade conspecific competitor populations |
| Q34481806 | Lionel Sharples Penrose, 1898-1972: A personal memoir in celebration of the centenary of his birth. |
| Q52935162 | Local similarity in evolutionary rates extends over whole chromosomes in human-rodent and mouse-rat comparisons: implications for understanding the mechanistic basis of the male mutation bias. |
| Q34921032 | Male-biased transmission of deleterious mutations to the progeny in Arabidopsis thaliana |
| Q35109500 | Male-male competition magnifies inbreeding depression in wild house mice |
| Q58042179 | Maternal age affects offspring lifespan of the seed beetle, Callosobruchus maculatus |
| Q33722046 | Maternal non-Mendelian inheritance of a reduced lifespan? A hypothesis |
| Q62964509 | Meiotic silencing by unpaired DNA |
| Q28741124 | Meta-analysis of paternal age and schizophrenia risk in male versus female offspring |
| Q34096157 | Microsatellite mutations in the germline: implications for evolutionary inference |
| Q46353594 | Modeling the maternal-age dependency of reproductive failure and genetic fitness |
| Q50930753 | Molecular evolution--who is in the driver's seat? |
| Q37856457 | Molecular population genomics: a short history |
| Q33651160 | Mutation Size Optimizes Speciation in an Evolutionary Model |
| Q28389468 | Mutation and Human Exceptionalism: Our Future Genetic Load |
| Q22011012 | Mutation enhancement by DINB1, a mammalian homologue of the Escherichia coli mutagenesis protein dinB |
| Q36283159 | Mutation frequency declines during spermatogenesis in young mice but increases in old mice |
| Q37117871 | Mutation load under additive fitness effects |
| Q34146302 | Mutation rates in humans. II. Sporadic mutation-specific rates and rate of detrimental human mutations inferred from hemophilia B. |
| Q42382061 | Mutation, Eugenics, and the Boundaries of Science |
| Q51721422 | Negative environmental perturbations may improve species persistence. |
| Q36853758 | Origins and consequences of DNA damage in male germ cells. |
| Q64095472 | Overlooked roles of DNA damage and maternal age in generating human germline mutations |
| Q73832606 | Oxidative stress in the male germ line and its role in the aetiology of male infertility and genetic disease |
| Q39341914 | PERSPECTIVE: SPONTANEOUS DELETERIOUS MUTATION. |
| Q38692051 | Parental Age and Offspring Psychopathology in the Philadelphia Neurodevelopmental Cohort |
| Q77493342 | Paternal age affects fertility and progeny outcome in the Brown Norway rat |
| Q24596212 | Paternal age and risk of schizophrenia in adult offspring |
| Q24561502 | Paternal age and schizophrenia: a population based cohort study |
| Q48680791 | Paternal age effect on age of onset in bipolar I disorder is mediated by sex and family history |
| Q47589125 | Paternal and maternal age as risk factors for schizophrenia: a case-control study |
| Q57239357 | Paternal and maternal ages at conception and risk of bipolar affective disorder in their offspring |
| Q34356609 | Paternal factors and schizophrenia risk: de novo mutations and imprinting |
| Q28138231 | Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome |
| Q33938164 | Paternal transmission of genetic damage: findings in animals and humans |
| Q36870022 | Phenotypically distinct subtypes of psychosis accompany novel or rare variants in four different signaling genes |
| Q41739794 | Population genetics: surviving under mutation pressure |
| Q34280525 | Prenatal and perinatal risk factors for autism in China |
| Q36720684 | Preservation of methylated CpG dinucleotides in human CpG islands |
| Q28678675 | Properties and rates of germline mutations in humans |
| Q28755128 | Quantifying the threat of extinction from Muller's ratchet in the diploid Amazon molly (Poecilia formosa) |
| Q36716123 | Rapid decline of fitness in panmictic populations of Drosophila melanogaster maintained under relaxed natural selection. |
| Q33667179 | Rate, molecular spectrum, and consequences of human mutation |
| Q24633781 | Rates and fitness consequences of new mutations in humans |
| Q24548000 | Rates of spontaneous mutation |
| Q24812652 | Reactive oxygen species in spermatozoa: methods for monitoring and significance for the origins of genetic disease and infertility |
| Q43463309 | Risk of autism associated with general anesthesia during cesarean delivery: a population-based birth-cohort analysis |
| Q48018626 | Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations |
| Q92205734 | Schizophrenia: update on genetics, cognitive behavioural therapy and early intervention |
| Q46229578 | Senescent sperm performance in old male birds |
| Q73428625 | Sex and U |
| Q50856271 | Sex biases in the mutation rate. |
| Q80594044 | Sexual selection, redundancy and survival of the most beautiful |
| Q37106059 | Should autism be considered a canary bird telling that Homo sapiens may be on its way to extinction? |
| Q52572510 | Significance of the perigametic interval as a major source of spontaneous mutations that result in mosaics. |
| Q52693094 | Single-nucleotide mutation rate increases close to insertions/deletions in eukaryotes. |
| Q34604252 | Spectra of spontaneous frameshift mutations at the hisD3052 allele of Salmonella typhimurium in four DNA repair backgrounds |
| Q84321746 | Sperm DNA damage: correlation to severity of semen abnormalities |
| Q37789756 | Sperm donation in the United Kingdom in 2010 |
| Q35649504 | Spontaneous deleterious mutation in Arabidopsis thaliana |
| Q33698759 | Spontaneous mutation in man. |
| Q24619077 | Statement on guidance for genetic counseling in advanced paternal age |
| Q51819432 | Substitution rate heterogeneity and the male mutation bias. |
| Q42382062 | Taking Exception to Human Eugenics |
| Q34142204 | The X chromosome and the rate of deleterious mutations in humans |
| Q52006859 | The conservation of redundancy in genetic systems: effects of sexual and asexual reproduction. |
| Q92054415 | The deteriorating soma and the indispensable germline: gamete senescence and offspring fitness |
| Q38299878 | The disparity mutagenesis model predicts rescue of living things from catastrophic errors |
| Q22065135 | The distribution of fitness effects of new deleterious amino acid mutations in humans |
| Q28817127 | The effect of induced mutations on quantitative traits in Arabidopsis thaliana: Natural versus artificial conditions |
| Q35108676 | The effect of paternal age on offspring intelligence and personality when controlling for paternal trait level |
| Q39979716 | The effects of low-impact mutations in digital organisms |
| Q40241703 | The effects of reproduction on courtship, fertility and longevity within and between alternative male mating tactics of the horned beetle, Onthophagus binodis |
| Q46265868 | The fundamental theorem of natural selection with mutations |
| Q53671372 | The importance of advanced parental age in the origin of neurofibromatosis type 1. |
| Q28206110 | The origins, patterns and implications of human spontaneous mutation |
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| Q34218124 | Theoretical analysis of mutation hotspots and their DNA sequence context specificity |
| Q28768916 | There is no universal molecular clock for invertebrates, but rate variation does not scale with body size |
| Q47836425 | Unexpectedly similar rates of nucleotide substitution found in male and female hominids |
| Q41881742 | Unpredictable fitness transitions between haploid and diploid strains of the genetically loaded yeast Saccharomyces cerevisiae |
| Q73956230 | [Daltonism and the genetics of aging] |
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