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Connection

Molly Przeworski to Humans

This is a "connection" page, showing publications Molly Przeworski has written about Humans.
Connection Strength

0.731
  1. The clock-like accumulation of germline and somatic mutations can arise from the interplay of DNA damage and repair. PLoS Biol. 2024 Jun; 22(6):e3002678.
    View in: PubMed
    Score: 0.031
  2. 2023 ASHG Scientific Achievement Award. Am J Hum Genet. 2024 Mar 07; 111(3):425-427.
    View in: PubMed
    Score: 0.031
  3. Relating pathogenic loss-of-function mutations in humans to their evolutionary fitness costs. Elife. 2023 01 17; 12.
    View in: PubMed
    Score: 0.028
  4. A paternal bias in germline mutation is widespread in amniotes and can arise independently of cell division numbers. Elife. 2022 08 02; 11.
    View in: PubMed
    Score: 0.027
  5. Lottery, luck, or legacy. A review of "The Genetic Lottery: Why DNA matters for social equality". Evolution. 2022 04 01; 76(4):846-853.
    View in: PubMed
    Score: 0.027
  6. PRDM9 losses in vertebrates are coupled to those of paralogs ZCWPW1 and ZCWPW2. Proc Natl Acad Sci U S A. 2022 03 01; 119(9).
    View in: PubMed
    Score: 0.027
  7. Mutation saturation for fitness effects at human CpG sites. Elife. 2021 11 22; 10.
    View in: PubMed
    Score: 0.026
  8. The evolution of group differences in changing environments. PLoS Biol. 2021 01; 19(1):e3001072.
    View in: PubMed
    Score: 0.025
  9. A comparison of humans and baboons suggests germline mutation rates do not track cell divisions. PLoS Biol. 2020 08; 18(8):e3000838.
    View in: PubMed
    Score: 0.024
  10. Variable prediction accuracy of polygenic scores within an ancestry group. Elife. 2020 01 30; 9.
    View in: PubMed
    Score: 0.023
  11. Signatures of replication timing, recombination, and sex in the spectrum of rare variants on the human X chromosome and autosomes. Proc Natl Acad Sci U S A. 2019 09 03; 116(36):17916-17924.
    View in: PubMed
    Score: 0.022
  12. Overlooked roles of DNA damage and maternal age in generating human germline mutations. Proc Natl Acad Sci U S A. 2019 05 07; 116(19):9491-9500.
    View in: PubMed
    Score: 0.022
  13. Measuring intolerance to mutation in human genetics. Nat Genet. 2019 05; 51(5):772-776.
    View in: PubMed
    Score: 0.022
  14. Contrasting Determinants of Mutation Rates in Germline and Soma. Genetics. 2017 09; 207(1):255-267.
    View in: PubMed
    Score: 0.019
  15. Human Germline Mutation and the Erratic Evolutionary Clock. PLoS Biol. 2016 Oct; 14(10):e2000744.
    View in: PubMed
    Score: 0.018
  16. Variation in the molecular clock of primates. Proc Natl Acad Sci U S A. 2016 09 20; 113(38):10607-12.
    View in: PubMed
    Score: 0.018
  17. Interpreting the Dependence of Mutation Rates on Age and Time. PLoS Biol. 2016 Jan; 14(1):e1002355.
    View in: PubMed
    Score: 0.017
  18. An estimate of the average number of recessive lethal mutations carried by humans. Genetics. 2015 Apr; 199(4):1243-54.
    View in: PubMed
    Score: 0.016
  19. TroX: a new method to learn about the genesis of aneuploidy from trisomic products of conception. Bioinformatics. 2014 Jul 15; 30(14):2035-42.
    View in: PubMed
    Score: 0.015
  20. The convergent evolution of blue iris pigmentation in primates took distinct molecular paths. Am J Phys Anthropol. 2013 Jul; 151(3):398-407.
    View in: PubMed
    Score: 0.014
  21. Evaluating the evidence for transmission distortion in human pedigrees. Genetics. 2012 May; 191(1):215-32.
    View in: PubMed
    Score: 0.013
  22. Variation in human recombination rates and its genetic determinants. PLoS One. 2011; 6(6):e20321.
    View in: PubMed
    Score: 0.013
  23. Classic selective sweeps were rare in recent human evolution. Science. 2011 Feb 18; 331(6019):920-4.
    View in: PubMed
    Score: 0.012
  24. Genome-sequencing anniversary. The golden age of human population genetics. Science. 2011 Feb 04; 331(6017):547.
    View in: PubMed
    Score: 0.012
  25. Broad-scale recombination patterns underlying proper disjunction in humans. PLoS Genet. 2009 Sep; 5(9):e1000658.
    View in: PubMed
    Score: 0.011
  26. Natural selection on genes that underlie human disease susceptibility. Curr Biol. 2008 Jun 24; 18(12):883-9.
    View in: PubMed
    Score: 0.010
  27. The timing of selection at the human FOXP2 gene. Mol Biol Evol. 2008 Jul; 25(7):1257-9.
    View in: PubMed
    Score: 0.010
  28. High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans. Science. 2008 Mar 07; 319(5868):1395-8.
    View in: PubMed
    Score: 0.010
  29. An evolutionary view of human recombination. Nat Rev Genet. 2007 Jan; 8(1):23-34.
    View in: PubMed
    Score: 0.009
  30. How reliable are empirical genomic scans for selective sweeps? Genome Res. 2006 Jun; 16(6):702-12.
    View in: PubMed
    Score: 0.009
  31. Genetics. Motivating hotspots. Science. 2005 Oct 14; 310(5746):247-8.
    View in: PubMed
    Score: 0.009
  32. Causal interpretations of family GWAS in the presence of heterogeneous effects. Proc Natl Acad Sci U S A. 2024 Sep 17; 121(38):e2401379121.
    View in: PubMed
    Score: 0.008
  33. Insights into recombination from patterns of linkage disequilibrium in humans. Genetics. 2004 May; 167(1):387-97.
    View in: PubMed
    Score: 0.008
  34. Down the Penrose stairs, or how selection for fewer recombination hotspots maintains their existence. Elife. 2023 Oct 13; 12.
    View in: PubMed
    Score: 0.007
  35. Limited role of generation time changes in driving the evolution of the mutation spectrum in humans. Elife. 2023 02 13; 12.
    View in: PubMed
    Score: 0.007
  36. Evidence for population growth in humans is confounded by fine-scale population structure. Trends Genet. 2002 Nov; 18(11):559-63.
    View in: PubMed
    Score: 0.007
  37. The signature of positive selection at randomly chosen loci. Genetics. 2002 Mar; 160(3):1179-89.
    View in: PubMed
    Score: 0.007
  38. Impact of essential workers in the context of social distancing for epidemic control. PLoS One. 2021; 16(8):e0255680.
    View in: PubMed
    Score: 0.006
  39. Linkage disequilibrium in humans: models and data. Am J Hum Genet. 2001 Jul; 69(1):1-14.
    View in: PubMed
    Score: 0.006
  40. Why is there so little intragenic linkage disequilibrium in humans? Genet Res. 2001 Apr; 77(2):143-51.
    View in: PubMed
    Score: 0.006
  41. When did the human population size start increasing? Genetics. 2000 Aug; 155(4):1865-74.
    View in: PubMed
    Score: 0.006
  42. Adjusting the focus on human variation. Trends Genet. 2000 Jul; 16(7):296-302.
    View in: PubMed
    Score: 0.006
  43. Deconstructing the sources of genotype-phenotype associations in humans. Science. 2019 09 27; 365(6460):1396-1400.
    View in: PubMed
    Score: 0.006
  44. Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation. Elife. 2019 09 24; 8.
    View in: PubMed
    Score: 0.006
  45. The population genetics of human disease: The case of recessive, lethal mutations. PLoS Genet. 2017 Sep; 13(9):e1006915.
    View in: PubMed
    Score: 0.005
  46. Identifying genetic variants that affect viability in large cohorts. PLoS Biol. 2017 Sep; 15(9):e2002458.
    View in: PubMed
    Score: 0.005
  47. A genetic method for dating ancient genomes provides a direct estimate of human generation interval in the last 45,000 years. Proc Natl Acad Sci U S A. 2016 May 17; 113(20):5652-7.
    View in: PubMed
    Score: 0.004
  48. Variation in Rural African Gut Microbiota Is Strongly Correlated with Colonization by Entamoeba and Subsistence. PLoS Genet. 2015 Nov; 11(11):e1005658.
    View in: PubMed
    Score: 0.004
  49. Non-crossover gene conversions show strong GC bias and unexpected clustering in humans. Elife. 2015 Mar 25; 4.
    View in: PubMed
    Score: 0.004
  50. Footprints of ancient-balanced polymorphisms in genetic variation data from closely related species. Evolution. 2015 Feb; 69(2):431-46.
    View in: PubMed
    Score: 0.004
  51. Determinants of mutation rate variation in the human germline. Annu Rev Genomics Hum Genet. 2014; 15:47-70.
    View in: PubMed
    Score: 0.004
  52. Different selective pressures shape the evolution of Toll-like receptors in human and African great ape populations. Hum Mol Genet. 2013 Dec 01; 22(23):4829-40.
    View in: PubMed
    Score: 0.004
  53. Ancestry runs deeper than blood: the evolutionary history of ABO points to cryptic variation of functional importance. Bioessays. 2013 Oct; 35(10):862-7.
    View in: PubMed
    Score: 0.004
  54. Multiple instances of ancient balancing selection shared between humans and chimpanzees. Science. 2013 Mar 29; 339(6127):1578-82.
    View in: PubMed
    Score: 0.004
  55. A fine-scale chimpanzee genetic map from population sequencing. Science. 2012 Apr 13; 336(6078):193-8.
    View in: PubMed
    Score: 0.003
  56. The case of the fickle fingers: how the PRDM9 zinc finger protein specifies meiotic recombination hotspots in humans. PLoS Biol. 2011 Dec; 9(12):e1001211.
    View in: PubMed
    Score: 0.003
  57. PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice. Science. 2010 Feb 12; 327(5967):836-40.
    View in: PubMed
    Score: 0.003
  58. No effect of recombination on the efficacy of natural selection in primates. Genome Res. 2008 Apr; 18(4):544-54.
    View in: PubMed
    Score: 0.003
  59. Combining sperm typing and linkage disequilibrium analyses reveals differences in selective pressures or recombination rates across human populations. Genetics. 2007 Feb; 175(2):795-804.
    View in: PubMed
    Score: 0.002
  60. The rise and fall of the chemoattractant receptor GPR33. J Biol Chem. 2005 Sep 02; 280(35):31068-75.
    View in: PubMed
    Score: 0.002
  61. Fine-scale recombination patterns differ between chimpanzees and humans. Nat Genet. 2005 Apr; 37(4):429-34.
    View in: PubMed
    Score: 0.002
  62. Absence of the TAP2 human recombination hotspot in chimpanzees. PLoS Biol. 2004 Jun; 2(6):e155.
    View in: PubMed
    Score: 0.002
  63. Evidence for a complex demographic history of chimpanzees. Mol Biol Evol. 2004 May; 21(5):799-808.
    View in: PubMed
    Score: 0.002
  64. Loss of olfactory receptor genes coincides with the acquisition of full trichromatic vision in primates. PLoS Biol. 2004 Jan; 2(1):E5.
    View in: PubMed
    Score: 0.002
  65. A neutral explanation for the correlation of diversity with recombination rates in humans. Am J Hum Genet. 2003 Jun; 72(6):1527-35.
    View in: PubMed
    Score: 0.002
  66. Molecular evolution of FOXP2, a gene involved in speech and language. Nature. 2002 Aug 22; 418(6900):869-72.
    View in: PubMed
    Score: 0.002
  67. Evidence for positive selection and population structure at the human MAO-A gene. Proc Natl Acad Sci U S A. 2002 Jan 22; 99(2):862-7.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.