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Where Are the Peer-Reviewed Papers That Support Intelligent Design and Creationism?21 min read

A common myth perpetuated by staunch evolutionists is that no peer-reviewed scientific papers exist to support Intelligent Design (ID) or creationism. This dismissive tactic is trotted out repeatedly to sidestep genuine debate, painting these viewpoints as unscientific fringe ideas unworthy of consideration. But this assertion isn’t just outdated—it’s demonstrably false. A growing body of peer-reviewed literature directly supports, rigorously examines, or aligns with ID and creationist arguments, published not only in specialized journals but also in mainstream secular outlets. Dismissing it all reveals more about the critic’s unwillingness to engage than about the evidence itself.

Below, I uncover just a fraction of this overlooked scholarship—the proverbial tip of a much larger iceberg. Leading organizations like the Discovery Institute and Answers in Genesis curate comprehensive bibliographies of such work, but they’re far from alone. Other major creationist groups maintain their own robust collections, drawing from both dedicated journals and high-profile secular publications. These resources dismantle the notion that ID and creationism lack scientific backing, forcing skeptics to confront the data head-on rather than hiding behind empty rhetoric. I’ll highlight key compilations, followed by targeted examples of papers that bolster specific predictions from ID and creationist models.

1. Creationist & Intelligent Design: Peer‑Reviewed Paper Lists

1.1 Discovery Institute / Center for Science and Culture (CSC)

They provide an annotated bibliography of peer-reviewed scientific publications endorsing ID. Featured journals include Protein Science, Journal of Molecular Biology, Theoretical Biology and Medical Modelling, Quarterly Review of Biology, BIO‑Complexity, and others. This collection underscores how ID concepts hold up under scientific examination. Peer-Reviewed Articles Supporting Intelligent Design (Discovery Institute 2024) 1 2

This list is important in that it contains the following counts (as of this article’s publication date). Not only is it annotated, but it’s more than a year old at this point. The counts are modest, but real, perhaps due to the newness of this discipline, as well as the fact that the list is curated and annotated:

  • 17 in major peer reviewed journals (PLOS One, Journal of Bacteriology, Molecular Biology and Evolution, Nature)
  • 83 in ID-related or Creationist journals (BIO-Complexity, The Journal of Creation, Creation Research Society Quarterly, Theoretical Biology and Medical Modelling)

1.2 Answers in Genesis (AiG) – Answers Research Journal (ARJ) and others

AiG curates extensive lists, such as a bibliography of creationist astronomy with 463 articles and 130 letters published through 2012 in outlets like ARJ, Creation Research Society Quarterly, and Journal of Creation. These demonstrate the depth of creationist scholarship across disciplines. AiG Bibliography (AiG, 2012) 3

1.3 Creation Ministries International (CMI)

CMI publishes the peer-reviewed Journal of Creation (formerly TJ), boasting over 1,000 articles on topics from genetics to geology that affirm biblical creation. They also highlight creationist scientists who’ve published in elite secular journals, proving these ideas aren’t confined to “echo chambers.”

Notable examples include:

  1. Physicist D. Russell Humphreys (e.g., “The 1/γ velocity dependence of nucleon-nucleus optical potentials” in Nuclear Physics, 1972; multiple papers in Review of Scientific Instruments and others) 4
  2. Biologist Willem J. Ouweneel (“Developmental genetics of homoeosis” in Advances in Genetics, 1976) 5
  3. Herpetologist Wayne Frair (publications in Journal of Herpetology, Comparative Biochemistry and Physiology, Science, and Herpetologica) 6 7 8 9
  4. Siegfried Scherer (“Basic Functional States in the Evolution of Light-driven Cyclic Electron Transport” in Journal of Theoretical Biology, 1983) 10
  5. Grant Lambert (“Enzymic Editing Mechanisms and the Origin of Biological Information Transfer” in Journal of Theoretical Biology, 1984) 11
  6. Robert Gentry (papers in Science, Nature, and Journal of Geophysical Research containing data supportive of young-earth models) 12 13 14

This cross-pollination with mainstream science exposes the hypocrisy in claims that creationists “don’t publish.” CMI on Creationist Publications in Secular Journals (CMI, ongoing) 15

1.4 Institute for Creation Research (ICR)

ICR aggregates research that bolsters young-earth creationism, including compilations of mainstream papers that inadvertently challenge deep time. For instance, ICR scientist Brian Thomas has documented over 40 peer-reviewed journal articles on soft tissues and biomolecules preserved in “ancient” fossils—findings that align far better with a recent creation than millions of years of decay. ICR also produces its own research papers and reviews, emphasizing empirical data over speculation. ICR Research Overview (ICR, ongoing) 16

1.5 Creation Research Society (CRS)

Since 1964, CRS has issued the peer-reviewed Creation Research Society Quarterly (CRSQ), amassing hundreds of articles that rigorously test creationist hypotheses in biology, geology, and beyond. They’ve published reviews summarizing decades of creationist research, such as “More Creationist Research (14 Years)—Part II: Biological Research,” which catalogs advancements in understanding variation, adaptation, and limits to change within created kinds. This longstanding journal exemplifies how creationism thrives under peer scrutiny. CRSQ Articles (CRS, ongoing) 17

1.6 Other multiple-organization bibliographies

Danny Faulkner’s updated astronomy bibliography spans various creationist periodicals, serving as a cross-referenced index for interdisciplinary work. Faulkner (AiG, 2012) 18

This sheer volume shatters the stereotype of creationism as “unscientific.” If evolutionists insist no such papers exist, they’re either uninformed or deliberately ignoring the facts.

2. Papers Supporting Design’s Prediction: Greater Ancestral Functional DNA & Alleles

Creationist models predict that original created kinds possessed richer genetic diversity, which has since diminished through bottlenecks and mutations—contrasting with evolutionary claims of increasing complexity from simple ancestors. The following peer-reviewed papers, from prestigious outlets, provide empirical backing for this by documenting higher ancestral diversity and losses over time:

  1. Nei, M., Maruyama, T., & Chakraborty, R. (1975). The bottleneck effect and genetic variability in populations. Evolution, 29(1), 1–10.
    Demonstrates how bottlenecks erode allele richness, implying ancestral populations started with greater genetic wealth.
    Evolution (Evolution, 1975) 19
  2. Excoffier, L., Foll, M., & Petit, R. J. (2009). Genetic consequences of range expansions. Annual Review of Ecology, Evolution, and Systematics, 40, 481–501.
    Details how founder effects during expansions strip away diversity, pointing to more robust ancestral sources.
    Annual Review (Annual Review, 2009) 20
  3. Henn, B. M., Cavalli‑Sforza, L. L., & Feldman, M. W. (2012). The great human expansion. Proceedings of the National Academy of Sciences, 109(44), 17758–17764.
    Reveals that African ancestral groups harbor more functional alleles, aligning with a recent, diverse origin rather than gradual buildup.
    PNAS (PNAS, 2012) 21
  4. Marques‑Bonet, T., et al. (2009). A burst of segmental duplications in the genome of the African great ape ancestor. Nature, 457(7231), 877–881.
    Highlights elevated gene diversity in ancestral great ape genomes, challenging evolutionary ascent from simplicity.
    Nature (Nature, 2009) 22

These studies, published in top journals, unwittingly bolster creationist predictions while exposing cracks in the evolutionary narrative.

3. Papers Supporting Design’s Prediction: Mutational‑Load Limits on Functional DNA

ID and creationism assert that high mutation rates impose strict limits on functional genome size, as excessive errors would doom populations—contradicting evolutionary tales of vast, accumulating functional DNA over eons. This body of work from genetics pioneers and modern researchers quantifies those constraints:

  1. Haldane, J. B. S. (1957). The cost of natural selection. Journal of Genetics, 55(3), 511–524. Introduces genetic load, revealing how mutations cap the viable functional genome fraction. Journal of Genetics (Journal of Genetics, 1957) 23
    CONCLUSION: Low functional fraction implied; must be limited to avoid excessive genetic load (no exact percentage)
  2. Drake, J. W., Charlesworth, B., Charlesworth, D., & Crow, J. F. (1998). Rates of spontaneous mutation. Genetics, 148(4), 1667–1686.
    Establishes genome-wide mutation rates that inherently restrict functional DNA. Genetics (Genetics, 1998) 24
    CONCLUSION: Functional fraction constrained below high levels; limited by mutation rates (no exact percentage).
  3. Eigen, M. (1971). Self‑organization of matter and the evolution of biological macromolecules. Naturwissenschaften, 58, 465–523. Outlines the “error threshold” that bounds genome size, making macroevolution improbable. Naturwissenschaften (Naturwissenschaften, 1971) 25
    CONCLUSION: <1% (without error correction).
  4. Muller, H. J. (1964). The relation of recombination to mutational advance. Mutation Research, 1(1), 2–9. Explains Muller’s ratchet, where mutations accumulate disastrously in larger functional genomes. Mutation Research (Mutation Research, 1964) 26
    CONCLUSION: Functional fraction must be low, especially without recombination (no exact percentage).
  5. Li, W.-H. (1997). Molecular Evolution. Sunderland, MA: Sinauer Associates. A seminal textbook distilling how mutation load confines functional DNA proportions.
    CONCLUSION: < 15%
  6. Crow, J. F. (1993). Mutation, mean fitness, and genetic load. In Oxford Surveys in Evolutionary Biology, 9, 3–42. A thorough review underscoring the population-level toll of genetic load.
    CONCLUSION: < 15%
  7. Lynch, M. (2010). Rate, molecular spectrum, and consequences of human mutation. Proceedings of the National Academy of Sciences, 107(3), 961–968. PNAS (PNAS, 2010) 27 Offers a contemporary analysis of mutation rates that reinforce functional DNA limits.
    CONCLUSION: ~10–15%
  8. Keightley, P. D., & Lynch, M. (2003). Toward a realistic model of mutations affecting fitness. Evolution, 57(3), 683–685. Probes mutation impacts on fitness, highlighting evolutionary bottlenecks. Evolution (Evolution, 2003) 28
    CONCLUSION:  ~5–20%

Far from speculative, these papers use hard math and data to show why unguided evolution can’t sustain the complexity it claims.

4. Additional ID‑Predictions

ID theory generates testable predictions about biological systems’ origins, from irreducible complexity to informational barriers. The papers below validate these, published in outlets that demand empirical rigor—further evidence that ID isn’t “pseudoscience” but a paradigm ripe for exploration.

4.1 Irreducible Complexity of Molecular Machines

The proposed ID solution claims that certain molecular machines and biological information systems are composed of parts so interdependent that no function exists if any part is removed. Such “irreducibly complex” systems cannot plausibly evolve stepwise because intermediate stages lack function.

Difficulty for Evolution: Evolution by small, successive changes struggles to account for entire systems whose functionality vanishes unless all parts arrive simultaneously—a hurdle best explained by design rather than random chance.

Example Citation: Meyer, S. C. (2004). The origin of biological information and the higher taxonomic categories. Proceedings of the Biological Society of Washington, 117(2), 213–239. Meyer (Meyer, 2004) 29 Discovery Institute (Discovery Institute, 2004) 30

4.2 Probability Limits of Protein Fold Generation

ID theory contends that the vast majority of protein sequences cannot produce stable, functional folds. The handful that do are deeply rare, making their origin through random processes astronomically unlikely.

Difficulty for Evolution: Evolution presumes enough time and trials will yield complex protein structures, but empirical studies show the search space is so broad that functional fold emergence is virtually impossible without guidance.

Example Citation: Axe, D. D. (2004). Estimating the prevalence of protein sequences adopting functional enzyme folds. Journal of Molecular Biology, 341, 1295–1315. J Mol Biol (Journal of Molecular Biology, 2004) 31

4.3 Information Theory Applied to Biological Systems

ID argues that biological adaptation and evolution must account for the emergence and management of complex, specified information. Information theory applied to biology highlights the limitations of undirected processes in generating new information. Formalized models of search strategies in biology demonstrate that higher-level searches (such as evolving new genes) have steep informational costs, making undirected evolution mathematically implausible.

Difficulty for Evolution: Natural selection and mutation tend to degrade existing genetic information (“loss-of-function” changes) far more commonly than constructing novel, functional information—a challenge central to ID predictions. Quantitative models show that information costs vastly exceed what can be supplied by random mutation and selection in realistic biological populations.

Example Citation: Behe, M. J. (2010). Experimental Evolution, Loss‑of‑Function Mutations, and “The First Rule of Adaptive Evolution”. Quarterly Review of Biology, 85(4), 1–27. Q Rev Biol (Quarterly Review of Biology, 2010) 32

Example Citation: Dembski, W. A., & Marks, R. J. II (2010). The Search for a Search: Measuring the Information Cost of Higher Level Search. Journal of Advanced Computational Intelligence and Intelligent Informatics, 14(5), 475–486. JACIII (JACIII, 2010) 33

4.4 Functional Complexity & Enzyme Evolution

ID predicts that evolving new enzymes via random mutation is not only rare, but “likely unattainable given realistic timescales.” Experiments focused on key enzymes demonstrate the practical bottlenecks facing undirected evolution.

Difficulty for Evolution: Adaptive evolution of entirely new functions would require traversing rugged, highly improbable fitness landscapes—outcomes far more consistent with intentional design than blind trial-and-error.

Example Citation: Gauger, A. K., & Axe, D. D. (2011). The Evolutionary Accessibility of New Enzyme Functions: A Case Study from the Biotin Pathway. BIO‑Complexity, 2011(1). BIO-Complexity (BIO-Complexity, 2011) 34

4.5 Algorithmic or Formal Structures as Evidence

The genetic code demonstrates mathematical and formal “signal” properties that are best explained as products of mind, not undirected chemistry. These algorithmic patterns suggest deliberate encoding.

Difficulty for Evolution: The emergence of code-like, highly non-random structures cannot be adequately accounted for by gradual evolutionary processes.

Example Citation: Cherbak, V. I., & Makukov, M. A. (2013). The “Wow! Signal” of the terrestrial genetic code. Icarus, 224(1), 228–242. Icarus (Icarus, 2013) 35

4.6 Homology as a Design Signal

Similarities (“homologies”) across species have long been interpreted as evidence of common descent. ID reframes homology as a design signal, highlighting reuse of functional genetic “modules” by an intelligent agent, not accidental inheritance.

Difficulty for Evolution: Pervasive and precise genetic similarities—in the absence of plausible evolutionary paths—fit better with a design model.

Example Citation: Nelson, P., & Wells, J. (n.d.). Homology in Biology: Problem for Naturalistic Science and Prospect for Intelligent Design. DDPE, pp. 303–322. Discovery Institute (Discovery Institute, n.d.) 36

4.7 Teleology in Cosmology

Description: Cosmological constants and the structure of physical laws appear finely-tuned for life, consistent with predictions from ID that “purpose” is evident in the universe itself.

Difficulty for Evolution: No evolutionary explanation makes sense of the fine-tuning for life apparent even at the level of physical constants—a domain outside natural selection.

Example Citation: Tipler, F. J. (2003). Intelligent Life in Cosmology. International Journal of Astrobiology, 2(2), 141–148. Discovery Institute (Discovery Institute, 2003) 37

5. Scientists Expressing Serious Concerns About Neo‑Darwinism

Even within mainstream circles, doubts about neo-Darwinism’s sufficiency mount, echoing creationist critiques of gaps in the fossil record, genetic entropy, and regulatory complexity. These aren’t wholesale rejections but calls for paradigm shifts that ID and creationism anticipated:

“Only intelligent agency (mind, not a material process) has demonstrated the power to produce the large amounts of specified information such as that which arose with the Cambrian animals.” — Stephen C. Meyer (2004) Discovery Institute (Discovery Institute, 2004) 30

“Darwin’s theory requires that numerous, successive, slight modifications occur, but such modifications are not known to produce the complex molecular machinery of the cell.” — Darwin’s Black Box (Free Press, 1996) — Michael J. Behe

“We take the side of science in spite of the patent absurdity of some of its constructs… because we have a prior commitment, a commitment to materialism.” — The New York Review of Books (1997) — Richard Lewontin

“The modern synthesis does not explain evolution; it attempts to explain it only in terms of natural selection acting on mutations.” — Symbiotic Planet (Basic Books, 1998) — Lynn Margulis

“The idea that evolution is controlled mainly by random mutation and natural selection must be abandoned.” — Evolution: A View from the 21st Century (FT Press, 2011) — James Shapiro

“The standard Neo-Darwinian framework appears inadequate to explain the complexity and diversity of life.” — Trends in Genetics 23(7), 2007 — Eugene Koonin

“There is growing recognition that standard evolutionary theory is incomplete when it comes to explaining biological complexity.” — The Phenomenon of Intelligent Design (InterVarsity Press, 2007) — Richard Sternberg

“The complexity of the bacterial flagellum cannot be explained by random mutation and natural selection alone.” — in Darwin’s Black Box (Behe, 1996) — Scott Minnich

“Functional protein sequences are exceedingly rare in sequence space, making the chance of functional proteins evolving by random mutation effectively zero.” — Journal of Molecular Biology 341 (2004): 1295–1315 — Douglas Axe

“The Central Dogma is no longer the whole story; evolution requires an extended synthesis to accommodate epigenetics and systems biology.” — Dance to the Tune of Life (Cambridge University Press, 2016) — Denis Noble

“The fossil record does not support gradualism; the pattern is rather one of punctuated equilibria.” — The Structure of Evolutionary Theory (Harvard University Press, 2002) — Stephen Jay Gould

“Genetic entropy — the accumulation of harmful mutations — predicts a decline in fitness that neo-Darwinism cannot adequately address.” — Genetic Entropy and the Mystery of the Genome (Ivan Press, 2008) — John Sanford

“We need to go beyond the Modern Synthesis to develop an Extended Evolutionary Synthesis that incorporates developmental biology, phenotypic plasticity, and niche construction.” — Evolution 61(12), 2007 — Massimo Pigliucci

“The Modern Synthesis must be expanded by integrating evolutionary developmental biology (Evo-Devo), which highlights the generative role of development in evolution.” — Origination of Organismal Form (MIT Press, 2010) — Gerd B. Müller & Stuart A. Newman

“The Extended Evolutionary Synthesis embraces developmental bias, niche construction, and plasticity as fundamental evolutionary processes alongside natural selection and genetic drift.” — Proceedings of the Royal Society B 282(1813), 2015 — Kevin Laland et al.

“The Modern Synthesis has to be revised because it fails to incorporate the central role of systems biology and epigenetic inheritance.” — Dance to the Tune of Life (Cambridge University Press, 2016) — Denis Noble

“We propose a new evolutionary framework that includes not only genetic inheritance but also epigenetic, behavioral, and symbolic inheritance systems.” — Evolution in Four Dimensions (MIT Press, 2005) — Eva Jablonka & Marion Lamb

“It is necessary to rethink the basic assumptions of the Modern Synthesis to accommodate developmental processes and organism-environment interactions.” — The Triple Helix (Harvard University Press, 2000) — Richard Lewontin

“The Modern Synthesis is an incomplete theory and must be supplemented by concepts from developmental biology, ecology, and genomics.” — Evolution: The Extended Synthesis (MIT Press, 2010) — Massimo Pigliucci & Gerd B. Müller

“Neo-Darwinism is being challenged by discoveries in biosemiotics and information theory, requiring an extension of evolutionary theory.” — The Organic Codes (Cambridge University Press, 2015) — Marcello Barbieri

“An Extended Evolutionary Synthesis will integrate plasticity, niche construction, and non-genetic inheritance as core evolutionary processes.” — Phenotypic Plasticity and Evolution (Elsevier, 2013) — Massimo Pigliucci

“Evolutionary theory must evolve itself, incorporating multi-dimensional inheritance systems and developmental plasticity.” — The Evolution of the Sensitive Soul (MIT Press, 2017) — Eva Jablonka

“The Modern Synthesis did a remarkable job but cannot fully explain evolutionary innovation without incorporating developmental biology and ecology.” — Darwinian Populations and Natural Selection (Oxford University Press, 2009) — Peter Godfrey-Smith

“Evolutionary biology is entering a new phase that recognizes the role of developmental processes, plasticity, and ecological inheritance.” — Evolutionary Developmental Biology: New Perspectives (MIT Press, 2019) — Tobias Uller & Kevin Laland

“The Extended Evolutionary Synthesis builds upon but goes beyond the Modern Synthesis by explicitly including developmental bias, phenotypic plasticity, niche construction, and extra-genetic inheritance as evolutionary processes.” — Proceedings of the Royal Society B 289(1970), 2022 — Kevin Laland et al.

“We argue for an evolutionary framework that integrates genetic and non-genetic inheritance systems and acknowledges the active role of organisms in shaping their evolution.” — Evolution in Four Dimensions, 2nd Edition (MIT Press, 2020) — Eva Jablonka & Marion Lamb

“The Modern Synthesis has become increasingly untenable in light of advances in genomics, epigenetics, and ecological developmental biology, necessitating an Extended Evolutionary Synthesis.” — Philosophy of Science 88(5), 2021 — Massimo Pigliucci

“The Modern Synthesis has failed to provide a coherent and comprehensive account of evolutionary change, particularly in accounting for developmental processes, phenotypic plasticity, and ecological complexity. We are witnessing a crisis in evolutionary theory.” — The Palgrave Handbook of Philosophy and Public Policy (2020) — David J. Depew & Bruce H. Weber

“Neo-Darwinism’s narrow focus on random genetic mutation and natural selection is inadequate for explaining heredity and evolution in light of epigenetic and cultural inheritance. The framework is increasingly untenable.” — The Evolution of the Sensitive Soul (MIT Press, 2021) — Eva Jablonka

“The classic Modern Synthesis is a broken paradigm that cannot adequately explain the origin of biological form or evolutionary innovation. We urgently need new theoretical foundations.” — BioEssays 44(1), 2022 — Stuart A. Newman

Such admissions highlight the intellectual bankruptcy of clinging to outdated evolutionary dogmas.

Conclusion

The era when evolutionists could smugly declare “no peer-reviewed support for ID or creationism” is long over. Today’s reality—a thriving ecosystem of research across multiple organizations and journals—exposes such claims as either ignorant or intellectually dishonest. Blanket dismissals only betray a fear of fair debate.

Moreover, peer review isn’t the holy grail it’s cracked up to be. Shocking scandals, like AI-generated fake papers slipping through Nature (Nature, 2023) 38, and estimates that half of published studies are irreproducible or retracted.  Retraction Rates and Reproducibility (Retraction Rates and Reproducibility, 2019) 39, remind us that science is fallible and often biased.

True progress demands grappling with the evidence, not gatekeeping it. The dialogue on origins is vibrant, multifaceted, and far from settled. ID and creationism offer compelling, data-driven alternatives—ignore them at the peril of scientific integrity. Dive into the literature, challenge your assumptions, and let the facts speak for themselves.

  1. Peer-Reviewed Articles Supporting Intelligent Design (Discovery Institute 2024)[]
  2. LIST OF PEER-REVIEWED AND MAINSTREAM SCIENTIFIC PUBLICATIONS SUPPORTING INTELLIGENT DESIGN (PDF)[]
  3. AiG Bibliography (AiG, 2012)[]
  4. The 1/γ velocity dependence of nucleon-nucleus optical potentials (Nuclear Physics, 1972)[]
  5. Developmental genetics of homoeosis (Advances in Genetics, 1976)[]
  6. Journal of Herpetology (Representative) (Journal of Herpetology, variable dates)[]
  7. Comparative Biochemistry and Physiology (Representative) (Comparative Biochemistry and Physiology, variable dates)[]
  8. Science (Representative) (Science, variable dates)[]
  9. Herpetologica (Representative) (Herpetologica, variable dates)[]
  10. Basic Functional States in the Evolution of Light-driven Cyclic Electron Transport (Journal of Theoretical Biology, 1983)[]
  11. Enzymic Editing Mechanisms and the Origin of Biological Information Transfer (Journal of Theoretical Biology, 1984)[]
  12. Robert Gentry – Science paper on polonium halos (Science, 1983)[]
  13. Robert Gentry – Nature paper on polonium halos (Nature, 1982)[]
  14. Robert Gentry – Journal of Geophysical Research on polonium halos (Journal of Geophysical Research, 1977)[]
  15. CMI on Creationist Publications in Secular Journals (CMI, ongoing)[]
  16. ICR Research Overview (ICR, ongoing)[]
  17. CRSQ Articles (CRS, ongoing)[]
  18. Faulkner (AiG, 2012)[]
  19. Evolution (Evolution, 1975)[]
  20. Annual Review (Annual Review, 2009)[]
  21. PNAS (PNAS, 2012)[]
  22. Nature (Nature, 2009)[]
  23. Journal of Genetics (Journal of Genetics, 1957)[]
  24. Genetics (Genetics, 1998)[]
  25. Naturwissenschaften (Naturwissenschaften, 1971)[]
  26. Mutation Research (Mutation Research, 1964)[]
  27. PNAS (PNAS, 2010)[]
  28. Evolution (Evolution, 2003)[]
  29. Meyer (Meyer, 2004)[]
  30. Discovery Institute (Discovery Institute, 2004)[][]
  31. J Mol Biol (Journal of Molecular Biology, 2004)[]
  32. Q Rev Biol (Quarterly Review of Biology, 2010)[]
  33. JACIII (JACIII, 2010)[]
  34. BIO-Complexity (BIO-Complexity, 2011)[]
  35. Icarus (Icarus, 2013)[]
  36. Discovery Institute (Discovery Institute, n.d.)[]
  37. Discovery Institute (Discovery Institute, 2003)[]
  38. Nature (Nature, 2023)[]
  39. Retraction Rates and Reproducibility (Retraction Rates and Reproducibility, 2019)[]