-
2
-
-
50449119163
-
Parental age and mutation
-
Penrose L. 1955 Parental age and mutation. Lancet 2, 312-313. (doi:10.1016/S0140-6736(55)92305-9)
-
(1955)
Lancet
, vol.2
, pp. 312-313
-
-
Penrose, L.1
-
4
-
-
0031778070
-
Mutation rate in human microsatellites: Influence of the structure and length of the tandem repeat
-
Brinkmann B, Klintschar M, Neuhuber F, Hühne J, Rolf B. 1998 Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Am. J. Hum. Genet. 62, 1408-1415. (doi:10.1086/301869)
-
(1998)
Am. J. Hum. Genet
, vol.62
, pp. 1408-1415
-
-
Brinkmann, B.1
Klintschar, M.2
Neuhuber, F.3
Hühne, J.4
Rolf, B.5
-
5
-
-
39049187468
-
Characteristics, causes and evolutionary consequences of male-based mutation
-
Ellegren H. 2007 Characteristics, causes and evolutionary consequences of male-based mutation. Proc. R. Soc. B 274, 1-10. (doi:10.1098/rspb.2006.3720)
-
(2007)
Proc. R. Soc. B
, vol.274
, pp. 1-10
-
-
Ellegren, H.1
-
6
-
-
77954562971
-
Haplotype-assisted characterization of germline mutations at short tandem repeat loci
-
Müller M, Sibbing U, Hohoff C, Brinkmann B. 2010 Haplotype-assisted characterization of germline mutations at short tandem repeat loci. Int. J. Legal Med. 124, 177-182. (doi:10.1007/s00414-009-0377-0)
-
(2010)
Int. J. Legal Med
, vol.124
, pp. 177-182
-
-
Müller, M.1
Sibbing, U.2
Hohoff, C.3
Brinkmann, B.4
-
7
-
-
84899077299
-
Cellular evidence for selfish spermatogonial selection in aged human testes
-
Maher GJ, Goriely A, Wilkie AO. 2014 Cellular evidence for selfish spermatogonial selection in aged human testes. Andrology 2, 304-314. (doi:10.1111/j.2047-2927.2013.00175.x)
-
(2014)
Andrology
, vol.2
, pp. 304-314
-
-
Maher, G.J.1
Goriely, A.2
Wilkie, A.O.3
-
8
-
-
84856922362
-
Paternal age effect mutations and selfish spermatogonial selection: Causes and consequences for human disease
-
Goriely A, Wilkie AO. 2012 Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease. Am. J. Hum. Genet. 90, 175-200. (doi:10.1016/j.ajhg.2011.12.017)
-
(2012)
Am. J. Hum. Genet
, vol.90
, pp. 175-200
-
-
Goriely, A.1
Wilkie, A.O.2
-
9
-
-
44949106318
-
Estimating cell depth from somatic mutations
-
Wasserstrom A et al. 2008 Estimating cell depth from somatic mutations. PLoS Comput. Biol. 4, e1000058. (doi:10.1371/journal.pcbi.1000058)
-
(2008)
Plos Comput. Biol
, vol.4
-
-
Wasserstrom, A.1
-
12
-
-
0037109017
-
Natural radioactivity and human mitochondrial DNA mutations
-
Forster L, Forster P, Lutz-Bonengel S, Willkomm H, Brinkmann B. 2002 Natural radioactivity and human mitochondrial DNA mutations. Proc. Natl Acad. Sci. USA 99, 13 950-13 954. (doi:10.1073/pnas.202400499)
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, Issue.13
-
-
Forster, L.1
Forster, P.2
Lutz-Bonengel, S.3
Willkomm, H.4
Brinkmann, B.5
-
13
-
-
84879756120
-
Somatic mutation, genomic variation, and neurological disease
-
Poduri A, Evrony GD, Cai X, Walsh CA. 2013 Somatic mutation, genomic variation, and neurological disease. Science 341, 1237758. (doi:10.1126/science.1237758)
-
(2013)
Science
, vol.341
-
-
Poduri, A.1
Evrony, G.D.2
Cai, X.3
Walsh, C.A.4
-
14
-
-
33747377545
-
Meiosis study in a population sample from Afghanistan: Allele frequencies and mutation rates of 16 STR loci
-
Hohoff C, Schürenkamp M, Börchers T, Eppink M, Brinkmann B. 2006 Meiosis study in a population sample from Afghanistan: allele frequencies and mutation rates of 16 STR loci. Int. J. Legal Med. 120, 300-302. (doi:10.1007/s00414-006-0091-0)
-
(2006)
Int. J. Legal Med
, vol.120
, pp. 300-302
-
-
Hohoff, C.1
Schürenkamp, M.2
Börchers, T.3
Eppink, M.4
Brinkmann, B.5
-
15
-
-
34548127657
-
Y-chromosomal microsatellite mutation rates in a population sample from northwestern Germany
-
Hohoff C, Dewa K, Sibbing U, Hoppe K, Forster P, Brinkmann B. 2007 Y-chromosomal microsatellite mutation rates in a population sample from northwestern Germany. Int. J. Legal Med. 121, 359-363. (doi:10.1007/s00414-006-0123-9)
-
(2007)
Int. J. Legal Med
, vol.121
, pp. 359-363
-
-
Hohoff, C.1
Dewa, K.2
Sibbing, U.3
Hoppe, K.4
Forster, P.5
Brinkmann, B.6
-
16
-
-
67349193312
-
Meiosis study in a population sample from Nigeria: Allele frequencies and mutation rates of 16 STR loci
-
Hohoff C, Schürenkamp M, Brinkmann B. 2009 Meiosis study in a population sample from Nigeria: allele frequencies and mutation rates of 16 STR loci. Int. J. Legal Med. 123, 259-261. (doi:10.1007/s00414-008-0307-6)
-
(2009)
Int. J. Legal Med
, vol.123
, pp. 259-261
-
-
Hohoff, C.1
Schürenkamp, M.2
Brinkmann, B.3
-
17
-
-
11144279421
-
Allelic drop-out in the STR system ACTBP2 (SE33) as a result of mutations in the primer binding region
-
Heinrich M, Müller M, Rand S, Brinkmann B, Hohoff C. 2004 Allelic drop-out in the STR system ACTBP2 (SE33) as a result of mutations in the primer binding region. Int. J. Legal Med. 118, 361-363. (doi:10.1007/s00414-004-0473-0)
-
(2004)
Int. J. Legal Med
, vol.118
, pp. 361-363
-
-
Heinrich, M.1
Müller, M.2
Rand, S.3
Brinkmann, B.4
Hohoff, C.5
-
18
-
-
24344447343
-
Characterisation of variant alleles in the STR systems D2S1338, D3S1358 and D19S433
-
Heinrich M, Felske-Zech H, Brinkmann B, Hohoff C. 2005 Characterisation of variant alleles in the STR systems D2S1338, D3S1358 and D19S433. Int. J. Legal Med. 119, 310-313. (doi:10.1007/s00414-005-0554-8)
-
(2005)
Int. J. Legal Med
, vol.119
, pp. 310-313
-
-
Heinrich, M.1
Felske-Zech, H.2
Brinkmann, B.3
Hohoff, C.4
-
19
-
-
9144259580
-
Haplotype studies support slippage as the mechanism of germline mutations in short tandem repeats
-
Klintschar M, Dauber EM, Ricci U, Cerri N, Immel UD, Kleiber M, Mayr WR. 2004 Haplotype studies support slippage as the mechanism of germline mutations in short tandem repeats. Electrophoresis 25, 3344-3348. (doi:10.1002/elps.200406069)
-
(2004)
Electrophoresis
, vol.25
, pp. 3344-3348
-
-
Klintschar, M.1
Dauber, E.M.2
Ricci, U.3
Cerri, N.4
Immel, U.D.5
Kleiber, M.6
Mayr, W.R.7
-
20
-
-
0032786945
-
Transmission ratio distortion at the INS-IGF2 VNTR
-
Eaves IA et al. 1999 Transmission ratio distortion at the INS-IGF2 VNTR. Nat. Genet. 22, 325. (doi:10.1038/11892)
-
(1999)
Nat. Genet
, vol.22
, pp. 325
-
-
Eaves, I.A.1
-
21
-
-
0012214335
-
Zur Theorie des Vaterschaftsnachweises auf Grund von Ähnlichkeitsbefunden Dtsch
-
Essen-Möller E, Quensel CE. 1939 Zur Theorie des Vaterschaftsnachweises auf Grund von Ähnlichkeitsbefunden Dtsch. Z. Ges. Gerichtl. Med. 31, 70-96.
-
(1939)
Z. Ges. Gerichtl. Med
, vol.31
, pp. 70-96
-
-
Essen-Möller, E.1
Quensel, C.E.2
-
22
-
-
34548413672
-
ISFG: Recommendations on biostatistics in paternity testing
-
Gjertson DW et al. 2007 ISFG: Recommendations on biostatistics in paternity testing. Forensic Sci. Int. Genet. 1, 223-231. (doi:10.1016/j.fsigen.2007.06.006)
-
(2007)
Forensic Sci. Int. Genet
, vol.1
, pp. 223-231
-
-
Gjertson, D.W.1
-
23
-
-
0005990524
-
How to deal with mutations in DNA testing
-
(eds C Rittner, PM Schneider, Berlin, Germany: Springer
-
Fimmers R, Henke L, Henke J, Baur M. 1992 How to deal with mutations in DNA testing. In Advances in forensic haemogenetics 4 (eds C Rittner, PM Schneider), pp. 285-287. Berlin, Germany: Springer.
-
(1992)
Advances in Forensic Haemogenetics
, vol.4
, pp. 285-287
-
-
Fimmers, R.1
Henke, L.2
Henke, J.3
Baur, M.4
-
24
-
-
0033911546
-
Surnames and the Y chromosome
-
Sykes B, Irven C. 2000 Surnames and the Y chromosome. Am. J. Hum. Genet. 66, 1417-1419. (doi:10.1086/302850)
-
(2000)
Am. J. Hum. Genet
, vol.66
, pp. 1417-1419
-
-
Sykes, B.1
Irven, C.2
-
25
-
-
0027161022
-
Mutation of human short tandem repeats
-
Weber JL, Wong C. 1993 Mutation of human short tandem repeats. Hum. Mol. Genet. 2, 1123-1128. (doi:10.1093/hmg/2.8.1123)
-
(1993)
Hum. Mol. Genet
, vol.2
, pp. 1123-1128
-
-
Weber, J.L.1
Wong, C.2
-
26
-
-
20444503008
-
Paternal age and intelligence: Implications for age-related genomic changes in male germ cells
-
Malaspina D et al. 2005 Paternal age and intelligence: implications for age-related genomic changes in male germ cells. Psychiatr. Genet. 15, 117-125. (doi:10.1097/00041444-200506000-00008)
-
(2005)
Psychiatr. Genet
, vol.15
, pp. 117-125
-
-
Malaspina, D.1
-
27
-
-
74949143588
-
Paternal factors and low birthweight, preterm, and small for gestational age births: A systematic review
-
Knowledge Synthesis Group on determinants of preterm/low birthweight births
-
Shah PS, Knowledge Synthesis Group on determinants of preterm/low birthweight births. 2010 Paternal factors and low birthweight, preterm, and small for gestational age births: a systematic review. Am. J. Obstet. Gynecol. 202, 103-123. (doi:10.1016/j.ajog.2009.08.026)
-
(2010)
Am. J. Obstet. Gynecol
, vol.202
, pp. 103-123
-
-
Shah, P.S.1
-
28
-
-
80052238644
-
Meta-analysis of paternal age and schizophrenia risk in male versus female offspring
-
Miller B et al. 2011 Meta-analysis of paternal age and schizophrenia risk in male versus female offspring. Schizophr. Bull. 37, 1039-1047. (doi:10.1093/schbul/sbq011)
-
(2011)
Schizophr. Bull
, vol.37
, pp. 1039-1047
-
-
Miller, B.1
-
29
-
-
84886801096
-
Parental age and risk of autism spectrum disorders in a Finnish national birth cohort
-
Lampi KM, Hinkka-Yli-SalomÄki S, Lehti V, Helenius H, Gissler M, Brown AS, Sourander A. 2013 Parental age and risk of autism spectrum disorders in a Finnish national birth cohort. J. Autism Dev. Disord. 43, 2526-2535. (doi:10.1007/s10803-013-1801-3)
-
(2013)
J. Autism Dev. Disord
, vol.43
, pp. 2526-2535
-
-
Lampi, K.M.1
Hinkka-Yli-Salomäki, S.2
Lehti, V.3
Helenius, H.4
Gissler, M.5
Brown, A.S.6
Sourander, A.7
-
30
-
-
34247849401
-
Paternal age and birth defects: How strong is the association?
-
Yang Q, Wen SW, Leader A, Chen XK, Lipson J, Walker M. 2007 Paternal age and birth defects: how strong is the association? Hum. Reprod. 22, 696-701. (doi:10.1093/humrep/del453)
-
(2007)
Hum. Reprod
, vol.22
, pp. 696-701
-
-
Yang, Q.1
Wen, S.W.2
Leader, A.3
Chen, X.K.4
Lipson, J.5
Walker, M.6
-
31
-
-
0001387585
-
Spermatogenesis in man: An estimate of its duration
-
Heller CG, Clermont Y. 1963 Spermatogenesis in man: an estimate of its duration. Science 140, 184-186. (doi:10.1126/science.140.3563.184)
-
(1963)
Science
, vol.140
, pp. 184-186
-
-
Heller, C.G.1
Clermont, Y.2
-
32
-
-
33751221301
-
A revised model for spermatogonial expansion in man: Lessons from non-human primates
-
Ehmcke J, Schlatt S. 2006 A revised model for spermatogonial expansion in man: lessons from non-human primates. Reproduction 132, 673-680. (doi:10.1530/rep.1.01081)
-
(2006)
Reproduction
, vol.132
, pp. 673-680
-
-
Ehmcke, J.1
Schlatt, S.2
-
33
-
-
45749083393
-
DNA double-strand break repair in parental chromatin of mouse zygotes, the first cell cycle as an origin of de novo mutation
-
Derijck A, van der Heijden G, Giele M, Philippens M, de Boer P. 2008 DNA double-strand break repair in parental chromatin of mouse zygotes, the first cell cycle as an origin of de novo mutation. Hum. Mol. Genet. 17, 1922-1937. (doi:10.1093/hmg/ddn090)
-
(2008)
Hum. Mol. Genet
, vol.17
, pp. 1922-1937
-
-
Derijck, A.1
Van Der Heijden, G.2
Giele, M.3
Philippens, M.4
De Boer, P.5
-
34
-
-
84866912512
-
A direct characterization of human mutation based on microsatellites
-
Sun JX et al. 2012 A direct characterization of human mutation based on microsatellites. Nat. Genet. 44, 1161-1167. (doi:10.1038/ng.2398)
-
(2012)
Nat. Genet
, vol.44
, pp. 1161-1167
-
-
Sun, J.X.1
-
35
-
-
84865208871
-
Rate of de novo mutations and the importance of father’s age to disease risk
-
Kong A et al. 2012 Rate of de novo mutations and the importance of father’s age to disease risk. Nature 488, 471-475. (doi:10.1038/nature11396)
-
(2012)
Nature
, vol.488
, pp. 471-475
-
-
Kong, A.1
-
36
-
-
84905579746
-
Whole-genome sequence variation, population structure and demographic history of the Dutch population
-
The Genome of the Netherlands Consortium
-
The Genome of the Netherlands Consortium. 2014 Whole-genome sequence variation, population structure and demographic history of the Dutch population. Nat. Genet. 46, 818-825. (doi:10.1038/ng.3021)
-
(2014)
Nat. Genet
, vol.46
, pp. 818-825
-
-
-
37
-
-
85020738055
-
New insights on human de novo mutation rate and parental age
-
October 2014, San Diego, USA
-
Wong WSW, Solomon B, Bodian D, Thach D, Iyer R, Vockley J, Niederhuber J. 2014 New insights on human de novo mutation rate and parental age. In American Society of Human Genetics Conference, October 2014, San Diego, USA.
-
(2014)
American Society of Human Genetics Conference
-
-
Wong, W.1
Solomon, B.2
Bodian, D.3
Thach, D.4
Iyer, R.5
Vockley, J.6
Niederhuber, J.7
-
38
-
-
84896720508
-
Germline quality control: EEF2 K stands guard to eliminate defective oocytes
-
Chu HP et al. 2014 Germline quality control: eEF2 K stands guard to eliminate defective oocytes. Dev. Cell 28, 561-572. (doi:10.1016/j.devcel.2014.01.027)
-
(2014)
Dev. Cell
, vol.28
, pp. 561-572
-
-
Chu, H.P.1
|