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

Year Number of Results
1800 1
1801 3
1803 2
1804 1
1805 1
1806 1
1928 1
1929 1
1931 1
1933 2
1934 2
1942 1
1944 1
1945 1
1946 2
1947 3
1949 4
1950 1
1951 3
1952 2
1953 2
1954 4
1955 2
1956 3
1957 5
1958 3
1959 1
1960 3
1961 4
1962 4
1963 5
1964 3
1965 2
1966 1
1967 4
1968 4
1969 1
1971 4
1972 5
1973 5
1974 3
1975 6
1976 7
1977 5
1978 3
1979 5
1980 2
1981 2
1982 4
1983 6
1984 12
1985 6
1986 10
1987 6
1988 9
1989 8
1990 4
1991 7
1992 6
1993 7
1994 8
1995 10
1996 3
1997 3
1998 11
1999 8
2000 5
2001 4
2002 5
2004 6
2005 4
2006 4
2007 8
2008 5
2009 8
2010 8
2011 4
2012 6
2013 7
2014 6
2015 8
2016 4
2017 7
2018 5
2019 6
2020 15
2021 14
2022 10
2023 21
2024 16

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434 results

Results by year

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Page 1
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
Rots D, Jakub TE, Keung C, Jackson A, Banka S, Pfundt R, de Vries BBA, van Jaarsveld RH, Hopman SMJ, van Binsbergen E, Valenzuela I, Hempel M, Bierhals T, Kortüm F, Lecoquierre F, Goldenberg A, Hertz JM, Andersen CB, Kibæk M, Prijoles EJ, Stevenson RE, Everman DB, Patterson WG, Meng L, Gijavanekar C, De Dios K, Lakhani S, Levy T, Wagner M, Wieczorek D, Benke PJ, Lopez Garcia MS, Perrier R, Sousa SB, Almeida PM, Simões MJ, Isidor B, Deb W, Schmanski AA, Abdul-Rahman O, Philippe C, Bruel AL, Faivre L, Vitobello A, Thauvin C, Smits JJ, Garavelli L, Caraffi SG, Peluso F, Davis-Keppen L, Platt D, Royer E, Leeuwen L, Sinnema M, Stegmann APA, Stumpel CTRM, Tiller GE, Bosch DGM, Potgieter ST, Joss S, Splitt M, Holden S, Prapa M, Foulds N, Douzgou S, Puura K, Waltes R, Chiocchetti AG, Freitag CM, Satterstrom FK, De Rubeis S, Buxbaum J, Gelb BD, Branko A, Kushima I, Howe J, Scherer SW, Arado A, Baldo C, Patat O, Bénédicte D, Lopergolo D, Santorelli FM, Haack TB, Dufke A, Bertrand M, Falb RJ, Rieß A, Krieg P, Spranger S, Bedeschi MF, Iascone M, Josephi-Taylor S, Roscioli T, Buckley MF, Liebelt J, Dagli AI, Aten E, Hurst ACE, Hicks A, Suri M, Aliu E, Naik S, Sidlow R, Coursimault J, Ni… See abstract for full author list ➔ Rots D, et al. Among authors: patterson wg. Am J Hum Genet. 2023 Jun 1;110(6):963-978. doi: 10.1016/j.ajhg.2023.04.008. Epub 2023 May 16. Am J Hum Genet. 2023. PMID: 37196654 Free PMC article.
Favre-Racouchot disease.
Patterson WM, Fox MD, Schwartz RA. Patterson WM, et al. Int J Dermatol. 2004 Mar;43(3):167-9. doi: 10.1111/j.1365-4632.2004.01546.x. Int J Dermatol. 2004. PMID: 15009383 Review.
The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8.
Dingemans AJM, Truijen KMG, van de Ven S, Bernier R, Bongers EMHF, Bouman A, de Graaff-Herder L, Eichler EE, Gerkes EH, De Geus CM, van Hagen JM, Jansen PR, Kerkhof J, Kievit AJA, Kleefstra T, Maas SM, de Man SA, McConkey H, Patterson WG, Dobson AT, Prijoles EJ, Sadikovic B, Relator R, Stevenson RE, Stumpel CTRM, Heijligers M, Stuurman KE, Löhner K, Zeidler S, Lee JA, Lindy A, Zou F, Tedder ML, Vissers LELM, de Vries BBA. Dingemans AJM, et al. Among authors: patterson wg. Transl Psychiatry. 2022 Oct 1;12(1):421. doi: 10.1038/s41398-022-02189-1. Transl Psychiatry. 2022. PMID: 36182950 Free PMC article.
Body dysmorphic disorder.
Patterson WM, Bienvenu OJ, Chodynicki MP, Janniger CK, Schwartz RA. Patterson WM, et al. Int J Dermatol. 2001 Nov;40(11):688-90. doi: 10.1046/j.1365-4362.2001.01168.x. Int J Dermatol. 2001. PMID: 11737433 Review. No abstract available.
Hyponatremia with venlafaxine.
Masood GR, Karki SD, Patterson WR. Masood GR, et al. Among authors: patterson wr. Ann Pharmacother. 1998 Jan;32(1):49-51. doi: 10.1345/aph.17117. Ann Pharmacother. 1998. PMID: 9475820
Occupational hazards to hospital personnel.
Patterson WB, Craven DE, Schwartz DA, Nardell EA, Kasmer J, Noble J. Patterson WB, et al. Ann Intern Med. 1985 May;102(5):658-80. doi: 10.7326/0003-4819-102-5-658. Ann Intern Med. 1985. PMID: 3885818 Review.
Hematologic effects of heavy metal poisoning.
Ringenberg QS, Doll DC, Patterson WP, Perry MC, Yarbro JW. Ringenberg QS, et al. Among authors: patterson wp. South Med J. 1988 Sep;81(9):1132-9. doi: 10.1097/00007611-198809000-00016. South Med J. 1988. PMID: 3047880 Review.
DNA methylation episignature in Gabriele-de Vries syndrome.
Cherik F, Reilly J, Kerkhof J, Levy M, McConkey H, Barat-Houari M, Butler KM, Coubes C, Lee JA, Le Guyader G, Louie RJ, Patterson WG, Tedder ML, Bak M, Hammer TB, Craigen W, Démurger F, Dubourg C, Fradin M, Franciskovich R, Frengen E, Friedman J, Palares NR, Iascone M, Misceo D, Monin P, Odent S, Philippe C, Rouxel F, Saletti V, Strømme P, Thulin PC, Sadikovic B, Genevieve D. Cherik F, et al. Among authors: patterson wg. Genet Med. 2022 Apr;24(4):905-914. doi: 10.1016/j.gim.2021.12.003. Epub 2022 Jan 10. Genet Med. 2022. PMID: 35027293 Free article.
434 results