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Erbkrankheiten in endogamen Populationen (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Erbkrankheiten in endogamen Populationen" in German language version.

refsWebsite
Global rank German rank
24nih.gov
4th place
7th place
13zdb-katalog.de
123rd place
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11doi.org
2nd place
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1nature.com
234th place
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1karger.com
4,489th place
3,288th place
1web.archive.org
1st place
1st place
1bmj.com
1,226th place
1,116th place

bmj.com

jmg.bmj.com

doi.org

  • K. B. McKusick, S. R. Schach, J. H. Koeslag: Social mechanisms in the population genetics of Tay-Sachs and other lethal autosomal recessive diseases: a computer simulation model. In: American journal of medical genetics. Band 36, Nummer 2, Juni 1990, S. 178–182, ISSN 0148-7299. doi:10.1002/ajmg.1320360211. PMID 2368806.
  • A. L. Price, A. Helgason, S. Palsson, H. Stefansson, D. St Clair, O. A. Andreassen, D. Reich, A. Kong, K. Stefansson: The impact of divergence time on the nature of population structure: an example from Iceland. In: PLoS genetics. Band 5, Nummer 6, Juni 2009, S. e1000505, ISSN 1553-7404. doi:10.1371/journal.pgen.1000505. PMID 19503599. PMC 2684636 (freier Volltext).
  • A. Helgason, B. Yngvadóttir, B. Hrafnkelsson, J. Gulcher, K. Stefánsson: An Icelandic example of the impact of population structure on association studies. In: Nature genetics. Band 37, Nummer 1, Januar 2005, S. 90–95, ISSN 1061-4036. doi:10.1038/ng1492. PMID 15608637.
  • S. Beleza, J. Campos, J. Lopes, I. I. Araújo, A. Hoppfer Almada, A. Correia e Silva, E. J. Parra, J. Rocha: The admixture structure and genetic variation of the archipelago of Cape Verde and its implications for admixture mapping studies. In: PloS one. Band 7, Nummer 11, 2012, S. e51103, ISSN 1932-6203. doi:10.1371/journal.pone.0051103. PMID 23226471. PMC 3511383 (freier Volltext).
  • K. Kristiansson, J. Naukkarinen, L. Peltonen: Isolated populations and complex disease gene identification. In: Genome Biol. (2008), Band 9, Nr. 8, S. 109. doi:10.1186/gb-2008-9-8-109. PMID 18771588; PMC 2575505 (freier Volltext).
  • A. D. Overall: The influence of the wahlund effect on the consanguinity hypothesis: consequences for recessive disease incidence in a socially structured pakistani population. In: Hum Hered. (2009), Band 67, Nr. 2, S. 140–144. doi:10.1159/000179561. PMID 19077430.
  • T. J. Pemberton, F. Y. Li, E. K. Hanson, N. U. Mehta, S. Choi, J. Ballantyne, J. W. Belmont, N. A. Rosenberg, C. Tyler-Smith, P. I. Patel: Impact of restricted marital practices on genetic variation in an endogamous Gujarati group. In: Am J Phys Anthropol. (2012), Band 149, Nr. 1, S. 92–103. doi:10.1002/ajpa.22101. PMID 22729696; PMC 3436606 (freier Volltext).
  • N. Ben Halim, N. Ben Alaya Bouafif, L. Romdhane, R. Kefi Ben Atig, I. Chouchane, Y. Bouyacoub, I. Arfa, W. Cherif, S. Nouira, F. Talmoudi, K. Lasram, S. Hsouna, W. Ghazouani, H. Azaiez, L. El Matri, A. Abid, N. Tebib, M. F. Ben Dridi, S. Kachboura, A. Amouri, M. Mokni, S. Ben Arab, K. Dellagi, S. Abdelhak: Consanguinity, endogamy, and genetic disorders in Tunisia. In: J Community Genet. (2013), Band 4, Nr. 2, S. 273–284. doi:10.1007/s12687-012-0128-7. PMID 23208456; PMC 3666836 (freier Volltext).
  • N. C. Orton, A. M. Innes, A. E. Chudley, N. T. Bech-Hansen: Unique disease heritage of the Dutch-German Mennonite population. In: American journal of medical genetics. Part A. Band 146A, Nummer 8, April 2008, S. 1072–1087, ISSN 1552-4833. doi:10.1002/ajmg.a.32061. PMID 18348259. (Review).
  • H. Ostrer, K. Skorecki: The population genetics of the Jewish people. In: Human genetics. Band 132, Nummer 2, Februar 2013, S. 119–127, ISSN 1432-1203. doi:10.1007/s00439-012-1235-6. PMID 23052947. PMC 3543766 (freier Volltext). (Review).
  • A. M. Laberge: [Prevalence and distribution of genetic diseases in Quebec: impact of the past on the present]. In: Médecine sciences : M/S. Band 23, Nummer 11, November 2007, S. 997–1001, ISSN 0767-0974. doi:10.1051/medsci/20072311997. PMID 18021714.

karger.com

  • C. Bellis, R. M. Hughes, K. N. Begley, S. Quinlan, R. A. Lea, S. C. Heath, J. Blangero, L. R. Griffiths: Phenotypical characterisation of the isolated norfolk island population focusing on epidemiological indicators of cardiovascular disease. In: Hum Hered. (2005), Band 60, Nr. 4, S. 211–219. PMID 16391489. PDF.

nature.com

  • J. Zlotogora: Multiple mutations responsible for frequent genetic diseases in isolated populations. In: Eur J Hum Genet. (2007), Band 15, Nr. 3, S. 272–278. PMID 17213840. PDF.

nih.gov

ncbi.nlm.nih.gov

  • E. O’Brien, R. A. Kerber, L. B. Jorde, A. R. Rogers: Founder effect: assessment of variation in genetic contributions among founders. In: Human biology. Band 66, Nummer 2, April 1994, S. 185–204, ISSN 0018-7143. PMID 8194843.
  • A. D. Overall, M. Ahmad, R. A. Nichols: The effect of reproductive compensation on recessive disorders within consanguineous human populations. In: Heredity. Band 88, Nummer 6, Juni 2002, S. 474–479, ISSN 0018-067X. PMID 12180090.
  • K. B. McKusick, S. R. Schach, J. H. Koeslag: Social mechanisms in the population genetics of Tay-Sachs and other lethal autosomal recessive diseases: a computer simulation model. In: American journal of medical genetics. Band 36, Nummer 2, Juni 1990, S. 178–182, ISSN 0148-7299. doi:10.1002/ajmg.1320360211. PMID 2368806.
  • A. L. Price, A. Helgason, S. Palsson, H. Stefansson, D. St Clair, O. A. Andreassen, D. Reich, A. Kong, K. Stefansson: The impact of divergence time on the nature of population structure: an example from Iceland. In: PLoS genetics. Band 5, Nummer 6, Juni 2009, S. e1000505, ISSN 1553-7404. doi:10.1371/journal.pgen.1000505. PMID 19503599. PMC 2684636 (freier Volltext).
  • A. Helgason, B. Yngvadóttir, B. Hrafnkelsson, J. Gulcher, K. Stefánsson: An Icelandic example of the impact of population structure on association studies. In: Nature genetics. Band 37, Nummer 1, Januar 2005, S. 90–95, ISSN 1061-4036. doi:10.1038/ng1492. PMID 15608637.
  • V. Safti?, D. Rudan, L. Zgaga: Mendelian diseases and conditions in Croatian island populations: historic records and new insights. In: Croatian medical journal. Band 47, Nummer 4, August 2006, S. 543–552, ISSN 1332-8166. PMID 16909451. PMC 2080446 (freier Volltext).
  • J. Zlotogora: Multiple mutations responsible for frequent genetic diseases in isolated populations. In: Eur J Hum Genet. (2007), Band 15, Nr. 3, S. 272–278. PMID 17213840. PDF.
  • J. S. Jones: How different are human races? In: Nature (1981), Band 293, Nr. 5829, S. 188–190. PMID 7278976.
  • S. Eickhoff, P. Beighton: Genetic disorders on the island of St Helena. In: S Afr Med J. (1985), Band 68, Nr. 7, S. 475–478. PMID 4049161.
  • C. Bellis, R. M. Hughes, K. N. Begley, S. Quinlan, R. A. Lea, S. C. Heath, J. Blangero, L. R. Griffiths: Phenotypical characterisation of the isolated norfolk island population focusing on epidemiological indicators of cardiovascular disease. In: Hum Hered. (2005), Band 60, Nr. 4, S. 211–219. PMID 16391489. PDF.
  • S. Beleza, J. Campos, J. Lopes, I. I. Araújo, A. Hoppfer Almada, A. Correia e Silva, E. J. Parra, J. Rocha: The admixture structure and genetic variation of the archipelago of Cape Verde and its implications for admixture mapping studies. In: PloS one. Band 7, Nummer 11, 2012, S. e51103, ISSN 1932-6203. doi:10.1371/journal.pone.0051103. PMID 23226471. PMC 3511383 (freier Volltext).
  • K. Kristiansson, J. Naukkarinen, L. Peltonen: Isolated populations and complex disease gene identification. In: Genome Biol. (2008), Band 9, Nr. 8, S. 109. doi:10.1186/gb-2008-9-8-109. PMID 18771588; PMC 2575505 (freier Volltext).
  • A. D. Overall: The influence of the wahlund effect on the consanguinity hypothesis: consequences for recessive disease incidence in a socially structured pakistani population. In: Hum Hered. (2009), Band 67, Nr. 2, S. 140–144. doi:10.1159/000179561. PMID 19077430.
  • T. J. Pemberton, F. Y. Li, E. K. Hanson, N. U. Mehta, S. Choi, J. Ballantyne, J. W. Belmont, N. A. Rosenberg, C. Tyler-Smith, P. I. Patel: Impact of restricted marital practices on genetic variation in an endogamous Gujarati group. In: Am J Phys Anthropol. (2012), Band 149, Nr. 1, S. 92–103. doi:10.1002/ajpa.22101. PMID 22729696; PMC 3436606 (freier Volltext).
  • N. M. Ghiasvand, E. Shirzad, M. Naghavi, M. R. Vaez Mahdavi: High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population. In: American journal of medical genetics. Band 78, Nummer 3, Juli 1998, S. 226–232, ISSN 0148-7299. PMID 9677055.
  • N. Ben Halim, N. Ben Alaya Bouafif, L. Romdhane, R. Kefi Ben Atig, I. Chouchane, Y. Bouyacoub, I. Arfa, W. Cherif, S. Nouira, F. Talmoudi, K. Lasram, S. Hsouna, W. Ghazouani, H. Azaiez, L. El Matri, A. Abid, N. Tebib, M. F. Ben Dridi, S. Kachboura, A. Amouri, M. Mokni, S. Ben Arab, K. Dellagi, S. Abdelhak: Consanguinity, endogamy, and genetic disorders in Tunisia. In: J Community Genet. (2013), Band 4, Nr. 2, S. 273–284. doi:10.1007/s12687-012-0128-7. PMID 23208456; PMC 3666836 (freier Volltext).
  • K. B. Gomes, V. C. Pardini, A. C. Ferreira, C. G. Fonseca, A. P. Fernandes: Founder effect of the 669insA mutation in BSCL2 gene causing Berardinelli-Seip congenital lipodystrophy in a cluster from Brazil. In: Ann Hum Genet. (2007), Band 71, Teil 6, S. 729–734. PMID 17535271.
  • K. Sleegers, G. Roks, J. Theuns, Y. S. Aulchenko, R. Rademakers, M. Cruts, W. A. van Gool, C. Van Broeckhoven, P. Heutink, B. A. Oostra, J. C. van Swieten, C. M. van Duijn: Familial clustering and genetic risk for dementia in a genetically isolated Dutch population. In: Brain (2004), Band 127, Teil 7, S. 1641–1649. PMID 15130954 (freier Volltextzugriff).
  • M. Payne, C. A. Rupar, G. M. Siu, V. M. Siu: Amish, mennonite, and hutterite genetic disorder database. In: Paediatrics & child health. Band 16, Nummer 3, März 2011, S. e23–e24, ISSN 1918-1485. PMID 22379385. PMC 3077314 (freier Volltext).
  • N. C. Orton, A. M. Innes, A. E. Chudley, N. T. Bech-Hansen: Unique disease heritage of the Dutch-German Mennonite population. In: American journal of medical genetics. Part A. Band 146A, Nummer 8, April 2008, S. 1072–1087, ISSN 1552-4833. doi:10.1002/ajmg.a.32061. PMID 18348259. (Review).
  • H. Ostrer, K. Skorecki: The population genetics of the Jewish people. In: Human genetics. Band 132, Nummer 2, Februar 2013, S. 119–127, ISSN 1432-1203. doi:10.1007/s00439-012-1235-6. PMID 23052947. PMC 3543766 (freier Volltext). (Review).
  • F. Bauduer: [History of biological anthropology of the Basque population: empiricism with molecular genetics]. In: Histoire des sciences médicales. Band 42, Nummer 2, 2008 Apr-Jun, S. 123–130, ISSN 0440-8888. PMID 19230313.
  • A. M. Laberge: [Prevalence and distribution of genetic diseases in Quebec: impact of the past on the present]. In: Médecine sciences : M/S. Band 23, Nummer 11, November 2007, S. 997–1001, ISSN 0767-0974. doi:10.1051/medsci/20072311997. PMID 18021714.
  • Gerald D. Hart: The Habsburg jaw. In: Canadian Medical Association journal. Band 104, Nummer 7, April 1971, S. 601–603, PMID 4927696, PMC 1930988 (freier Volltext)

web.archive.org

zdb-katalog.de

  • E. O’Brien, R. A. Kerber, L. B. Jorde, A. R. Rogers: Founder effect: assessment of variation in genetic contributions among founders. In: Human biology. Band 66, Nummer 2, April 1994, S. 185–204, ISSN 0018-7143. PMID 8194843.
  • A. D. Overall, M. Ahmad, R. A. Nichols: The effect of reproductive compensation on recessive disorders within consanguineous human populations. In: Heredity. Band 88, Nummer 6, Juni 2002, S. 474–479, ISSN 0018-067X. PMID 12180090.
  • K. B. McKusick, S. R. Schach, J. H. Koeslag: Social mechanisms in the population genetics of Tay-Sachs and other lethal autosomal recessive diseases: a computer simulation model. In: American journal of medical genetics. Band 36, Nummer 2, Juni 1990, S. 178–182, ISSN 0148-7299. doi:10.1002/ajmg.1320360211. PMID 2368806.
  • A. L. Price, A. Helgason, S. Palsson, H. Stefansson, D. St Clair, O. A. Andreassen, D. Reich, A. Kong, K. Stefansson: The impact of divergence time on the nature of population structure: an example from Iceland. In: PLoS genetics. Band 5, Nummer 6, Juni 2009, S. e1000505, ISSN 1553-7404. doi:10.1371/journal.pgen.1000505. PMID 19503599. PMC 2684636 (freier Volltext).
  • A. Helgason, B. Yngvadóttir, B. Hrafnkelsson, J. Gulcher, K. Stefánsson: An Icelandic example of the impact of population structure on association studies. In: Nature genetics. Band 37, Nummer 1, Januar 2005, S. 90–95, ISSN 1061-4036. doi:10.1038/ng1492. PMID 15608637.
  • V. Safti?, D. Rudan, L. Zgaga: Mendelian diseases and conditions in Croatian island populations: historic records and new insights. In: Croatian medical journal. Band 47, Nummer 4, August 2006, S. 543–552, ISSN 1332-8166. PMID 16909451. PMC 2080446 (freier Volltext).
  • S. Beleza, J. Campos, J. Lopes, I. I. Araújo, A. Hoppfer Almada, A. Correia e Silva, E. J. Parra, J. Rocha: The admixture structure and genetic variation of the archipelago of Cape Verde and its implications for admixture mapping studies. In: PloS one. Band 7, Nummer 11, 2012, S. e51103, ISSN 1932-6203. doi:10.1371/journal.pone.0051103. PMID 23226471. PMC 3511383 (freier Volltext).
  • N. M. Ghiasvand, E. Shirzad, M. Naghavi, M. R. Vaez Mahdavi: High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population. In: American journal of medical genetics. Band 78, Nummer 3, Juli 1998, S. 226–232, ISSN 0148-7299. PMID 9677055.
  • M. Payne, C. A. Rupar, G. M. Siu, V. M. Siu: Amish, mennonite, and hutterite genetic disorder database. In: Paediatrics & child health. Band 16, Nummer 3, März 2011, S. e23–e24, ISSN 1918-1485. PMID 22379385. PMC 3077314 (freier Volltext).
  • N. C. Orton, A. M. Innes, A. E. Chudley, N. T. Bech-Hansen: Unique disease heritage of the Dutch-German Mennonite population. In: American journal of medical genetics. Part A. Band 146A, Nummer 8, April 2008, S. 1072–1087, ISSN 1552-4833. doi:10.1002/ajmg.a.32061. PMID 18348259. (Review).
  • H. Ostrer, K. Skorecki: The population genetics of the Jewish people. In: Human genetics. Band 132, Nummer 2, Februar 2013, S. 119–127, ISSN 1432-1203. doi:10.1007/s00439-012-1235-6. PMID 23052947. PMC 3543766 (freier Volltext). (Review).
  • F. Bauduer: [History of biological anthropology of the Basque population: empiricism with molecular genetics]. In: Histoire des sciences médicales. Band 42, Nummer 2, 2008 Apr-Jun, S. 123–130, ISSN 0440-8888. PMID 19230313.
  • A. M. Laberge: [Prevalence and distribution of genetic diseases in Quebec: impact of the past on the present]. In: Médecine sciences : M/S. Band 23, Nummer 11, November 2007, S. 997–1001, ISSN 0767-0974. doi:10.1051/medsci/20072311997. PMID 18021714.