Cellebiologi

Sven‑Olof Bohman and Peter K.A. Jensen: Morphometric Studies on the Lipid Droplets of the Interstitial Cell of the Renal Medulla in Different States of Diuresis. J. Ultrastruct. Res. 55, 182‑192 (1976).

Sven‑Olof Bohman and Peter K.A. Jensen: The Interstitial Cells in the Renal Medulla of Rat, Rabbit, and Gerbil. Light and Electron Microscope Studies of Animals in Different States of Diuresis. Cell Tiss. Res. 189, 1‑18 (1978).

Peter K.A. Jensen and A.J. Therkelsen: Cultivation at low temperature as a measure to prevent contamination with fibroblasts in epithelial cultures from human skin. J. Invest. Dermatol. 77, 210‑212 (1981).

Peter K.A. Jensen and A.J. Therkelsen: Selective inhibition of fibroblasts by spermine in primary cultures of normal human skin epithelial cells. In Vitro 18, 867‑871 (1982).

Peter K.A. Jensen, J.O.R. Nørgård, S. Pedersen, and L. Bolund: Morphological and functional differentiation in epithelial cultures obtained from human skin explants. Virchows Arch (Cell Pathol) 44, 305‑322 (1983.

Peter K.A. Jensen and N.O. Jacobsen: Studies of D‑amino acid oxidase activity in human epidermis and cultured human epidermal cells. Arch. Dermatol. Res. 276, 57‑64 (1984). 

Peter K.A. Jensen, S. Pedersen and L. Bolund: Basal cell subpopulations and cell cycle kinetics in human epidermal explant cultures. Cell Tissue Kinet. 18, 201‑215 (1985).

Peter K.A. Jensen, J.O.R. Nørgård and L. Bolund: Changes in basal cell sub­populations and tissue differentiation in human epidermal cultures treated with epidermal growth factor and cholera toxin. Virchows Arch. (Cell Pathol) 49, 325‑340 (1985). 

Peter K.A. Jensen and L. Bolund: Changes in proliferating cell subpopulations and mitotic activity in human epidermal cultures treated with epithelial growth inhibitors. J. Invest. Dermatol. 86: 46‑50 (1986).

A. Andreasen, Peter K.A. Jensen and E. Jacobsen: Cloning of cells from synovial membrane in the investigation of rheumatoid arthritis. Exp. Cell Biol. 54: 220‑224 (1986). 

Peter K.A. Jensen, C. Knudsen, S. Pedersen, and L. Bolund: Cell kinetically defined subpopulations of cultured human epidermal keratinocytes differ with respect to cell size and staining pattern with antikeratin antibodies. Epithelia 1, 307‑321 (1987).

Peter K.A. Jensen and L. Bolund: Low Ca2+ stripping of differentiating cell layers in human epidermal cultures: An in vitro model of epidermal regeneration. Exp. Cell Res. 175: 63‑73 (1988). 

Peter K.A. Jensen: Keratinernes molekylære biologi og betydning inden for klinisk tumordiagnostik. Ugeskr. Læg. 151: 680‑686 (1989).

Peter K.A. Jensen, J.O.R. Nørgård, C. Knudsen, V. Nielsen, and L. Bolund: Effects of extra‑ and intracellular calcium concentration of DNA replication, lateral growth, and differentiation of human epidermal cells in culture. Virchows Archiv B 59: 17‑25 (1990). 

T.G. Jensen, Peter K.A. Jensen, J.O.R. Nørgård, and L. Bolund: High‑frequency transfection of cultured human epidermal basal cells that differentiate to form a multilayered tissue. Exp. Cell Res. 189: 163‑168 (1990).

Peter K.A. Jensen, K. Elgjo, O.D. Laerum, and L. Bolund: Syynthetic epidermal pentapeptide and related growth regulatory peptides inhibit proliferation and enhance differentiation in primary and regenerating cultures of human epidermal keratinocy­tes. J. Cell Sci. 97: 51-58 (1990).  

Peter K.A. Jensen, S.J. Fey, P. Mose Larsen, J.O.R. Nørgård, and L. Bolund: Morphological differentiation   and changes in polypeptide synthesis pattern during regeneration of human epidermal tissue developed     in vitro. Differentiation 47: 37-48 (1991).

Peter K.A. Jensen and L. Bolund: Tissue culture of human epidermal keratinocytes: A differentiating model system for gene testing and somatic gene therapy. J. Cell Sci. 100: 255-259 (1991). 

M. Kristensen, K. Paludan, C.G. Larsen, C.O.C. Zachariae, B.W. Deleuran, Peter K.A. Jensen, P. Jørgensen, and K. Thestrup-Pedersen: Ouantitative determination of IL-1Ó-induced IL-8 mRNA levels in cultured human keratinocytes, dermal fibroblasts, endothelial cells, and monocytes. J. Invest. Dermatol. 97: 506-510 (1991).20.

Peter K.A. Jensen, J.O.R. Nørgård, and L. Bolund: Lateral growth and terminal differentiation during          repeated epidermal regeneration in vitro. Age dependence and modulation by cholera toxin. Virchows  Archiv B 62: 189-198 (1992). 

T.G. Jensen, U.B. Jensen, Peter K.A. Jensen, H.H. Ibsen, F. Brandrup, A. Ballabio, and L. Bolund: Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue cultured epidermis from patients with recessive X-linked ichthyosis. Exp. Cell Res. 209: 392-397 (1993).

U.B. Jensen, T.G. Jensen, Peter K.A. Jensen, J. Rygaard, H. Ørskov, B. Sehested Hansen, J. Fogh, S. Kølvrå, and L. Bolund: Gene transfer into human tissue cultured epidermis and its transplantation onto immunodeficient mice: An experimental model for somatic gene therapy. J. Invest. Dermatol. 103:391-394 (1994). 

 

Genetik

1.  Peter K.A. Jensen and P. Hansen: A Bisatellited marker chromosome in an infant with the caudal regression anomalad. Clin. Genet. 19, 126‑129 (1981). 

2.  Peter K.A. Jensen: Nerve Deafness, Optic Nerve Atrophy, and Dementia ‑ A new X‑linked Recessive Syndrome? Amer. J. Med. Genet. 9, 55‑60 (1981). 

3.  Peter K.A. Jensen, Kirsten Rasmussen og Poul Bro: Belastningen af genetiske sygdomme blandt indlagte på en regional børneafdeling. Ugeskr. Læger 144, 2489‑2492 (1982). 

4.  Peter K.A. Jensen, C. Junien, S. Despoisse, A. Bernsen, T. Thelle, U. Friedrich, A. de la Chapelle: Inverted tandem duplication of the short arm of chromosome 8: A non‑random de novo structural aberration in man. Localization of the gene for glu­tat­hione re­duc­­ta­se in sub­band 8p2­1.1. Ann. Ge­net. 25, 207‑211 (1982). 

5.  Peter K.A. Jensen, C. Junien, and A. de la Chapelle: Gene for glutathione reductase Localized to subband 8p21.1. Seventh International Workshop on Human Gene Mapping. Los Angeles Conference (1983). 

6.  U. Friedrich, N. Horn, Peter K.A. Jensen, C. Lundsteen, M. Mikkelsen, J. Mosbech, J. Nielsen, K.B. Nielsen, G.B. Petersen, J. Philip, K. Rasmussen, A.J. Therkelsen, N. Tommerup og P. Videbech: Forebyggende fosterkromosom­undersøgelser i Danmark. Ugeskr. Læger 145, 1760‑1762 (1983). 

7.  U. Friedrich and Peter K.A. Jensen: Limited use of chromosomal markers in prenatal diagnosis. Prenatal Diagnosis 3, 355‑356 (1983). 

8.  U. Friedrich, N. Horn, Peter K.A. Jensen, C. Lundsteen, M. Mikkelsen, J. Nielsen, K. Brøndum Nielsen, G.B. Petersen, J. Philip, K. Rasmussen, A.J. Therkelsen, N. Tom­merup og P. Videbech: Spontane aborter og dødfødsler i relation til prænatale under­søgelser i Danmark. Ugeskr. Læger 146, 1848‑ 1849 (1984). 

9.  U. Friedrich, Peter K.A. Jensen, G.B. Petersen, K. Rasmussen og A.J. Therkelsen: Prænatal genetisk diagnostik. Opgørelse af 12 års resultater. Ugeskr. Læger 146, 1844‑1848 (1984). 

10.Peter K.A. Jensen: A 5p;22q reciprocal translocation with a high risk for segregation of unbalanced offspring. Clin. Genet. 26, 252‑254 (1984). 

11. A.M. Møllekær, Peter K.A. Jensen, U. Friedrich and G.B. Petersen: Four cases of the prenatal diagnosis of trisomy 20 mosaicism with a follow up investigation. Clin. Genet. 26, 265‑268 (1984). 

12.S. Smidt‑Jensen, N. Hahnemann, Peter K.A. Jensen and A.J. Therkelsen: Experience with trans­abdominal fine needle biopsy from chorionic villi in the first trimester: an alternative to am­niocenthesis. Clin. Genet. 26, 272‑274 (1984).

13.Peter K.A. Jensen, N. Hahnemann, H. Rehder, E. Schwinger and U. Friedrich: Prenatal diagnosis of af 46,XX/47,XX,+12 mosaicism. Prenatal diagnosis 4, 307‑309 (1984). 

14.S. Smidt‑Jensen, N. Hahnemann, Peter K.A. Jensen, and A.J. Therkelsen: Transabdominal Chorionic Villi Sampling for First Trimester Fetal Diagnosis. In: M. Fraccaro et al. (eds): First Trimester Fetal Diagnosis. Springer‑Verlag Berlin Heidelberg 1985, pp. 51‑53. 

15.A.J. Therkelsen, Peter K.A. Jensen, J. Trier Hansen, S. Smidt‑ Jensen, and N. Hah­nemann: Choice of medium for Cultivation and 24‑Hour Incubation of Chorionic Villi: Selective Effects     in Vitro. In: M. Fraccaro et al. (eds.). First Trimester Fetal Diagnosis. Springer‑Verlag Berlin Heidelberg 1985, pp. 157‑160. 

16.S. Smidt‑Jensen, N. Hahnemann, J. Jariri, Peter K.A. Jensen, and A.J. Therkelsen: Transabdominal chorionic villus sampling for first trimester fetal diagnosis. First 26 pregnancies followed to term. Prenatal diagnosis. 6:125‑132 (1986). 

17.Peter K.A. Jensen, J.M. Hertz, and A.J. Therkelsen: Admixture of maternal metaphases in first trimester direct chromosome preparations? Prenatal Diagnosis 6: 383‑385 (1986). 

18.S. Kølvraa, T.A. Kruse, Peter K.A. Jensen, K.H. Linde, S.R. Vestergård, and L. Bolund: Close linkage between X‑linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11‑12. Hum. Genet. 74: 284‑287 (1986). 

19.J.M. Hertz, Peter K.A. Jensen, and A.J. Therkelsen: Convoluted Cells as a Marker for Maternal Cell Contamination in CVS Cultures. Clin. Genet. 31: 410‑412 (1987). 

20.Peter K.A. Jensen, J.M. Hertz, N. Hahnemann, S. Smidt‑Jensen og A.J. Therkelsen: Prænatal diagnostik i første trimester. Ugeskr. Læger 149: 718‑721 (1987). 

21.Peter K.A. Jensen, E. Reske‑Nielsen, O. Hein‑Sørensen, and M. Warburg: The Syndrome of Op­ticoacoustic Nerve Atrophy with Dementia. Am. J. Med. Gen. 28: 517‑518 (1987).

K. Baggesen, U. Friedrich, Peter K.A. Jensen, K. Rasmussen: Three Large Danish Families with Paracentric Inversion in the Short Arm of Chromosome No. 5. Ann. Genet. 31: 50‑52 (1988). 

23.A.J. Therkelsen, Peter K.A. Jensen, J.M. Hertz, S. Smidt‑Jensen, and N. Hahnemann: Prenatal Cytogenetic Diagnosis after Transabdominal Chorionic Villus Sampling in the first Trimester. Prenatal Diagnosis 8: 19‑31 (1988). 

24.E. Reske‑Nielsen, Peter K.A. Jensen, O. Hein‑Sørensen, and K. Abelskov: Cal­cification of the central nervous system in a new hereditary neurological syndrome. Acta Neuropathol. 75: 590‑596 (1988). 

25.J.M. Hertz, PeterK.A. Jensen, U. Henriques og S. Maigaard: Transabdominal chorion villus biopsi ved abnormt ultralydfund i 2. trimester. Ugeskr. Læger 152: 28‑30 (1990). 

26.S. Kølvraa, J. Koch, N. Gregersen, Peter K.A. Jensen, A.L. Jørgensen, K.B. Petersen, K. Rasmussen, and L. Bolund: Application of flourescence in situ hybridization techniques in clinical genetics: Use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectively. Clin. Genet. 39: 278-286 (1991). 

27.B.S. Andresen, I. Knudsen, Peter K.A. Jensen, K. Rasmussen, and N. Gregersen: Two novel nonradioactive polymerase chain reaction-based assays of dried blood spots, genomic DNA, or whole cells for fast, reliable detection of Z and S mutations in the  1-antitrypsin gene. Clin. Chem. 38: 2100-2107 (1992). 

28.C.A. Brandt, O. Kierkegaard, J. Hindkjær, Peter K.A. Jensen, S. Pedersen, and A.J. Therkelsen: Ring  chromosome 20 with loss of telomeric sequences detected by multicolour PRINS. Clin. Genet. 44: 26-31 (1993).

29.B. Hertz, C.A. Brandt, M.B. Petersen, S. Pedersen, U. König, H. Strømkjær, and Peter K.A. Jensen: Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21. Clin. Genet. 44: 89-94 (1993). 

30.B. Hertz, C.A. Brandt, M.B. Petersen, S. Pedersen, U. König, H. Strømkjær, and Peter K.A. Jensen: Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21. In: C.S. Bartsocas, and P. Beighton (eds.): Dysmorphology and Genetics of Cardiovascular Disorders. HTA Medical Publications, Athen 1994. 

31.N. Gregersen, V. Winter, Peter K.A. Jensen, A. Holmskov, S. Kølvraa, B.S. Andresen, E. Christensen, P. Bross, J.B. Lundemose, and M. Gregersen: Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhood. Prenatal Diagnosis 15: 82-86 (1995). 

32.P. Koefoed, J.E. Nielsen, L. Hasholt, Peter K.A. Jensen, K. Fenger, and S.A. Sørensen: The molecular diagnosis of spinocerebellar ataxia type 1 in patients with ataxia. Europ. J. Neurol. 4: 586-592 (1997). 

33.Peter K. A. Jensen: Kromosomafvigelser hos mennesket. Gads Forlag 1998, 140 sider. 

34.C.B. Sørensen, A.-S. Ladekjær-Mikkelsen, B.S. Andresen, F. Brandrup, N.K. Veien, S.K. Buus, I. Anton-Lamprecht, T.A. Kruse,  Peter K.A. Jensen, H. Eiberg, L. Bolund, and N. Gregersen: Identification of novel and known mutations in the genes for keratin 5 and 14 in Danish patients with epidermolysis bullosa simplex: Correlation between genotype and phenotype. J. Invest. Dermatol. 112:184-190 (1999). 

35.Silahtaroglu, F.A. Hol, Peter K.A. Jensen, M. Edel, H.-C. Duba, M.P.A. Geurds, N.V.A.M. Knoers, E.C.M. Mariman, Z. Tümer, G. Utermann, J. Wirth, M. Bugge, and N. Tommerup: Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome. Eur. J. Hum. Gen. 7: 68-76 (1999). 

36.J.M. Hertz og Peter K.A. Jensen: Klinisk genetisk afdeling, Århus Kommunehospital. Månedsskr. Prakt. Lægegern. 77: 175-188 (1999). 

     R.M. Plenge, L. Tranebjaerg, Peter K.A. Jensen, C. Schwartz, and H.F. Willard: Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation. Am. J. Hum. Genet. 64: 759-767 (1999).

J.M Hertz, Peter K.A. Jensen og L.A. Bolund. Gener og sygdom. Odontologi 2000: 69-84. Munksgaard 2000. 

39.Peter K.A. Jensen: Udforskningen af menneskets arvemasse. Tidsskrift for Sygeplejeforskning 16: 27-44 (2000). 

40.Peter K.A. Jensen, C.B. Sørensen, B.S. Andresen, F. Brandrup, N.K. Veien, S.K. Buus, N. Gregersen, and L. Bolund. Keratinsygdomme. Ugeskr. Læg. 162: 1867-1872 (2000). 

41.C.B. Sørensen, A.-S. Ladekjær-Mikkelsen, B.S. Andresen, F. Brandrup, N.K. Veien, S.K. Buus, I. Anton-Lamprecht, T. Kruse, Peter K.A. Jensen, H. Eiberg, L. Bolund, and N. Gregersen. Epidermolysis bullosa simplex. Korrelation mellem genotype og fænotype hos danske patienter. Ugeskr. Læg. 162: 1873-1876 (2000). 

42.L. Tranebjærg, Peter K.A. Jensen, M. van Ghelue. X-linked recessevie deafness-dystonia syndrome (Mohr-Tranebjærg syndrome). In: K. Kitamura, K.P. Steel (eds): Genetics in Otorhinolaryngology. Adv Otorhinolaryngol Basel, Karger 2000, 56: 176-180. 

43.M. Kirchhoff, H. Rose, J. Maahr, T. Gerdes, M. Bugge, N. Tommerup, Z. Tümer, J. Lespinasse, Peter K. A. Jensen, J. Wirth, C. Lundsteen. High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. Eur. J. Hum. Gen. 2000, 8: 661-668. 

44.M. Bugge, G. Bruun-Petersen, K. Brøndum-Nielsen, U. Friedrich, J. Hansen, G. Jensen, Peter K. A. Jensen, U. Kristoffersson, C. Lundsteen, E. Niebuhr, K.R. Rasmussen, K. Rasmussen, N. Tommerup. Disease associated balanced chromosome rearrangement: A resource for large scale genotype-phenotype delineation in man. J. Med. Genet. 2000, 37: 858-865. 

Peter K.A. Jensen. Prænatal genetisk diagnostik og risikoscreening af gravide. Medicus 2001, 31 (1): 15-19.

Olesen, C. Hansen, E. Bendsen, A.G. Byskov, E. Schwinger, I. Lopez-Pajares, Peter K.A. Jensen, U. Kristoffersen, R. Schubert, E. Van Assche, J. Wahlstroem, J. Lespinasse, N. Tommerup. Identification of human candidate genes for male infertility by digital differential display.  Mol. Hum. Reproduc. 2001, 7 (1): 11-20. 

47.Peter K. A. Jensen: Forebyggelse af medfødt mental retardering. I: Sygdomsforbyggelse – hverdag og visioner. Red.: H. Goldstein. Akademisk Forlag 2001, side 99-119. 

48.L. Tranebjærg, Peter K. A. Jensen, M. van Ghelue, C.L. Vnencak-Jones, S. Sund, K. Elgjo, J. Jakobsen, S. Lindal, M. Warburg, A. Fuglsang-Frederiksen, K. Skullerud. Neuronal cell death in te visual cortex is a prominent feature of te X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in te TIMM8a gene. Ophthalmic Genetics 2001, 22 (4): 207-223. 

49.P. Kumarathas, Peter K. A. Jensen, M. Houman, U. Friedrich: Microdissection and reverse painting. Reevaluation of three cases with structural abnormalities in chromosome 13. Int. J. Hum. Genet. 2 (1): 1-4, 2002. 

50.Peter K. A. Jensen: Monogent arvelige sygdomme. Ugeskr. Læg. 165: 805-809 (2003). 

51.Sørensen CB, Andresen BS, Jensen UB, Jensen TG, Jensen, PKA, Gregersen N and Bolund L: Functional testing of keratin 14 mutant proteins associated with the three major subtypes of epidermolysis bullosa simplex. Exp. Derm. 2003, 12, 472-479. 

52.Peter K. A. Jensen: Prænatal diagnostik og screening for Downs syndrom. Ugeskr. Læg. 166: 1115 (2004). 

53.Bache Iben, Peter K.A. Jensen et al. An excess of chromosome 1 breakpoints in male infertility. Eur. J. Hum. Gen. 12: 993-1000, 2004. 

54.Pedersen S, Jensen, LG, Peter K. A. Jensen: Molekylær karyotypering. Ugeskr. Læg. 168: 1232 (2006). 

55.Nørby S, Peter K. A. Jensen (red.): Medicinsk Genetik. Lærebog for medicinstuderende, FADL’s Forlag 2006. 

56.Hertz JM, Peter K. A. Jensen: Genetisk rådgivning. I: Nørby S, Peter K. A. Jensen (red.): Medicinsk Genetik. Lærebog for medicinstuderende, FADL’s Forlag 2006, side 145-153. 

57.Lundsteen C, Peter K. A. Jensen: Prænatal genetisk diagnostik. I: Nørby S, Peter K. A. Jensen (red.): Medicinsk Genetik. Lærebog for medicinstuderende, FADL’s Forlag 2006, side 155-173. 

58.Thomassen M, Kruse TA, Peter K. A. Jensen, Gerdes, A-M: A missense mutation in exon 13 in BRCA2, c.7235G>A, results in skipping of exon 13. Genetic Testing 10 (2): 116-120, 2006.

59.Tarp U, Peter K. A. Jensen: Hereditære bindevævssygdomme. I: Pødenphant J et al. (red.): Reumatologi, FADL’s Forlag 2006, side 487-493.

Lone Sunde, Peter K. A. Jensen: Genetisk rådgivning. Det klinisk genetiske laboratorium. Lægen i Midten 2 (1): 15-18, 2007. 

Øyen  N, Poulsen G, Boyd HA, Wohlfahrt J, Jensen PKA, Melbye M: Recurrence of congenital heart defects in families. Circulation 120: 295-301, 2009.

Øyen  N, Poulsen G, Boyd HA, Wohlfahrt J, Jensen PKA, Melbye M: National time trends in congenital heart defects, Denmark, 1977-2005. Am Heart J 157: 467-473, 2009.

Øyen  N, Poulsen G, Boyd HA, Wohlfahrt J, Jensen PKA, Melbye M: Recurrence of congenital heart defects in families. Circulation 120: 295-301, 2009.

Øyen  N, Poulsen G, Wohlfahrt J, Boyd HA, Jensen PKA, Melbye M: Recurrence of discordant congenital heart defects in families. Circ Cardiovasc Genet 3: 122-128, 2010.

Birkebæk, NH, Sørensen JS, Vikre-Jørgensen J. Jensen PKA, Pedersen O, Hansen T. A De Novo Whole GCK Gene Deletion Not Detected by Gene Sequencing, in a Boy with Phenotypic GCK Insufficiency. Case Reports in Genetics 2011: 1-3, 2011.

Peter K. A. Jensen: Kromosomafvigelser hos mennesket. Gyldendal 2011, 143 sider.

Nørby S, Peter K. A. Jensen (red.): Medicinsk Genetik. Lærebog for medicinstuderende, FADL’s Forlag.  2. udgave 2012.

Hertz JM, Kjærgaard, S, Peter K. A. Jensen: Genetisk rådgivning. I: Nørby S, Peter K. A. Jensen (red.): Medicinsk Genetik. Lærebog for medicinstuderende, FADL’s Forlag. 2. udgave 2012, side 163-171.

Peter K. A. Jensen, Petersen, OB: Prænatal genetisk diagnostik. I: Nørby S, Peter K. A. Jensen (red.): Medicinsk Genetik. Lærebog for medicinstuderende, FADL’s Forlag. 2. udgave 2012, side 173-193.

Antropologi

Peter K. A. Jensen: Menneskets oprindelse og  udvikling. Gads Forlag 1996, 349 sider.

Peter K. A. Jensen: Hvorfor bliver vi gamle? Futuriblerne 26 (3): 7-14 (1998).

Peter K.A. Jensen. Da mennesket blev til – oprindelsen af Homo sapiens. Del 1. Aktuel Naturvidenskab, No. 2, 2001.

Peter K.A. Jensen. Da mennesket blev til – oprindelsen af Homo sapiens. Del 2.  Aktuel Naturvidenskab, No. ?, 2001.

Peter K. A. Jensen: Menneskets oprindelse og  udvikling. 2. udgave. Gads Forlag 2001, 349 sider.

Børglum AD, Madsen B, Jensen PKA, Vernesi C and Barbujani G: Population genetic study of possible descendants of the Cimbri in Denmark and Italy. Biennial Books of EAA 2: 169-178, 2002. 

Peter K. A. Jensen: Slægtskabet mellem jøder og palæstinensere. Aktuel naturvidenskab 2002, nr. 2, side 21-23. 

Peter K. A. Jensen: Da mennesket blev menneske. 1. udgave. Gyldendal 2004, 334 sider. 

Peter K. A. Jensen: Myten om Syndfloden. Aktuel Naturvidenskab, No. 4, 2005.

Peter K. A. Jensen: Menneskets oprindelse og  udvikling. 3. udgave. Gyldendal 2005, 432 sider.

Peter K. A. Jensen: Dværgmennesket fra Flores – The Lost World. Aktuel Naturvidenskab, No. 2, 2006.

Peter K. A. Jensen: Mennesket – den genetiske arv. Aarhus Universitetsforlag 2006.

Anders D. Børglum, Cristiano Vernesi, Peter K.A. Jensen, Bo Madsen, Annette Haagerup, and Guido Barbujani: No signature of Y chromosomal resemblance between possible descendants of the Cimbri in Denmark and Northern Italy. Am J Phys Anthropol  132: 278-284, 2007.

Peter K. A. Jensen: Da mennesket blev menneske. 2. udgave. Gyldendal 2007, 311 sider.

Peter K. A. Jensen: Menneskets evolution. I: Biologisk Antropologi (Lynnerup N et al., eds.), side 175-205, Gyldendal 2008.

Peter K. A. Jensen: Menneskets genetiske variation. I: Biologisk Antropologi (Lynnerup N et al., eds.), side 207-226, Gyldendal 2008.

Peter K. A. Jensen: Hvordan kan den moderne genetik bidrage til belysning af menneskets udvikling? Dansk Naturhistorisk Forenings Årsskrift nr. 18 2007/2008, side 7-17.

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