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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1903 1
1917 1
1918 1
1922 1
1923 2
1924 1
1926 1
1927 1
1931 1
1932 1
1934 1
1935 2
1937 1
1938 1
1939 2
1941 1
1942 1
1943 1
1944 1
1945 1
1946 7
1947 3
1948 15
1949 4
1950 4
1951 5
1952 3
1953 7
1954 8
1955 9
1956 7
1957 10
1958 7
1959 10
1960 13
1961 6
1962 10
1963 27
1964 31
1965 32
1966 35
1967 58
1968 152
1969 161
1970 183
1971 283
1972 252
1973 265
1974 300
1975 374
1976 343
1977 370
1978 473
1979 478
1980 511
1981 524
1982 588
1983 607
1984 623
1985 661
1986 683
1987 708
1988 811
1989 989
1990 1101
1991 1226
1992 1452
1993 1776
1994 1830
1995 2086
1996 2220
1997 2470
1998 2884
1999 3107
2000 3623
2001 3814
2002 3906
2003 4091
2004 4397
2005 4668
2006 4879
2007 4856
2008 5086
2009 5275
2010 5714
2011 6000
2012 6411
2013 6504
2014 6699
2015 6726
2016 6223
2017 6035
2018 6035
2019 6377
2020 6972
2021 7263
2022 7227
2023 6389
2024 2152

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152,153 results

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Page 1
Mendelian inheritance revisited: dominance and recessiveness in medical genetics.
Zschocke J, Byers PH, Wilkie AOM. Zschocke J, et al. Nat Rev Genet. 2023 Jul;24(7):442-463. doi: 10.1038/s41576-023-00574-0. Epub 2023 Feb 20. Nat Rev Genet. 2023. PMID: 36806206 Review.
Understanding why some alleles are harmful in the heterozygous state - representing dominant inheritance - but others only with the biallelic presence of pathogenic variants - representing recessive inheritance - is particularly important when faced with the deluge of rare …
Understanding why some alleles are harmful in the heterozygous state - representing dominant inheritance - but others only with the b …
Autosomal Dominant Retinitis Pigmentosa.
Tsang SH, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:69-77. doi: 10.1007/978-3-319-95046-4_15. Adv Exp Med Biol. 2018. PMID: 30578488 Review.
More than 70 genes (over 3000 mutations) are known to cause non-syndromic retinitis pigmentosa (RP), including autosomal dominant (AD), autosomal recessive (AR), X-linked, and simplex forms (inheritance not known). ...
More than 70 genes (over 3000 mutations) are known to cause non-syndromic retinitis pigmentosa (RP), including autosomal dominant (AD …
A review of clinical characteristics and genetic backgrounds in Alport syndrome.
Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K. Nozu K, et al. Clin Exp Nephrol. 2019 Feb;23(2):158-168. doi: 10.1007/s10157-018-1629-4. Epub 2018 Aug 20. Clin Exp Nephrol. 2019. PMID: 30128941 Free PMC article. Review.
It is divided into three modes of inheritance, namely, X-linked Alport syndrome (XLAS), autosomal recessive AS (ARAS), and autosomal dominant AS (ADAS). XLAS is caused by pathogenic variants in COL4A5, while ADAS and ARAS are caused by those in COL4A3/COL4A4. ...Because of …
It is divided into three modes of inheritance, namely, X-linked Alport syndrome (XLAS), autosomal recessive AS (ARAS), and autosomal domi …
Environment dominates over host genetics in shaping human gut microbiota.
Rothschild D, Weissbrod O, Barkan E, Kurilshikov A, Korem T, Zeevi D, Costea PI, Godneva A, Kalka IN, Bar N, Shilo S, Lador D, Vila AV, Zmora N, Pevsner-Fischer M, Israeli D, Kosower N, Malka G, Wolf BC, Avnit-Sagi T, Lotan-Pompan M, Weinberger A, Halpern Z, Carmi S, Fu J, Wijmenga C, Zhernakova A, Elinav E, Segal E. Rothschild D, et al. Nature. 2018 Mar 8;555(7695):210-215. doi: 10.1038/nature25973. Epub 2018 Feb 28. Nature. 2018. PMID: 29489753
Human gut microbiome composition is shaped by multiple factors but the relative contribution of host genetics remains elusive. Here we examine genotype and microbiome data from 1,046 healthy individuals with several distinct ancestral origins who share a relatively common …
Human gut microbiome composition is shaped by multiple factors but the relative contribution of host genetics remains elusive. Here w …
Heredity, genes, and headache.
Barbas NR, Schuyler EA. Barbas NR, et al. Semin Neurol. 2006 Nov;26(5):507-14. doi: 10.1055/s-2006-951623. Semin Neurol. 2006. PMID: 17048152 Review.
Recent studies into the heritability of primary headache subtypes, migraine, cluster and tension headache, and conditions in which headache is a prominent feature, such as the mitochondrial disease, mitochondrial encephalopathy, lactic acidosis, and strokelike episodes, and the a …
Recent studies into the heritability of primary headache subtypes, migraine, cluster and tension headache, and conditions in which headache …
Further evidence for heredity of pterygium.
Romano V, Steger B, Kovacova A, Kaye SB, Willoughby CE. Romano V, et al. Ophthalmic Genet. 2016 Dec;37(4):434-436. doi: 10.3109/13816810.2015.1111911. Epub 2016 Mar 2. Ophthalmic Genet. 2016. PMID: 26933759
Familial occurrence of pterygium is rare but supports the concept that heredity may predispose the conjunctiva to react abnormally to atmospheric-environmental stimuli. We describe a two generation Caucasian family of five members from the United Kingdom, four of whom deve …
Familial occurrence of pterygium is rare but supports the concept that heredity may predispose the conjunctiva to react abnormally to …
Mechanisms of Mendelian dominance.
Veitia RA, Caburet S, Birchler JA. Veitia RA, et al. Clin Genet. 2018 Mar;93(3):419-428. doi: 10.1111/cge.13107. Epub 2017 Oct 26. Clin Genet. 2018. PMID: 28755412 Review.
Genetic dominance has long been considered as a qualitative reflection of interallelic interactions. ...Dominance can also be influenced by epistatic (interloci) interactions. ...
Genetic dominance has long been considered as a qualitative reflection of interallelic interactions. ...Dominance can also be …
Transgenerational inheritance: how impacts to the epigenetic and genetic information of parents affect offspring health.
Xavier MJ, Roman SD, Aitken RJ, Nixon B. Xavier MJ, et al. Hum Reprod Update. 2019 Sep 11;25(5):518-540. doi: 10.1093/humupd/dmz017. Hum Reprod Update. 2019. PMID: 31374565
However, rather than being adaptive, such variation may also generate a plethora of pathological disease states ranging from dominant genetic disorders to neurological conditions, including spontaneous schizophrenia and autism....
However, rather than being adaptive, such variation may also generate a plethora of pathological disease states ranging from dominant …
The origin of heredity in protocells.
West T, Sojo V, Pomiankowski A, Lane N. West T, et al. Philos Trans R Soc Lond B Biol Sci. 2017 Dec 5;372(1735):20160419. doi: 10.1098/rstb.2016.0419. Philos Trans R Soc Lond B Biol Sci. 2017. PMID: 29061892 Free PMC article.
These positive feedbacks enable the fastest-growing protocells to dominate the early ecosystem through a simple form of heredity. We propose that as new organics are produced inside the protocells, the localized high-energy environment is more likely to form ribonuc …
These positive feedbacks enable the fastest-growing protocells to dominate the early ecosystem through a simple form of heredity …
MS-based technologies for untargeted single-cell proteomics.
Beck L, Geiger T. Beck L, et al. Curr Opin Biotechnol. 2022 Aug;76:102736. doi: 10.1016/j.copbio.2022.102736. Epub 2022 May 26. Curr Opin Biotechnol. 2022. PMID: 35644059 Review.
Single-cell analyses characterize individual cells, allowing their clustering and characterization in an unsupervised manner. Single-cell genomics and transcriptomics dominate the field of single-cell analysis, however, these often do not accurately reflect cellular functi …
Single-cell analyses characterize individual cells, allowing their clustering and characterization in an unsupervised manner. Single-cell ge …
152,153 results
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