 Abnormalities, Multiple
"Abnormalities, Multiple" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
No definition found.
| Descriptor ID |
D000015
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| MeSH Number(s) |
C16.131.077
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Abnormalities, Multiple".
Below are MeSH descriptors whose meaning is more specific than "Abnormalities, Multiple".
This graph shows the total number of publications written about "Abnormalities, Multiple" by people in this website by year, and whether "Abnormalities, Multiple" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1981 | 1 | 0 | 1 | | 1982 | 1 | 0 | 1 | | 1983 | 1 | 3 | 4 | | 1984 | 1 | 1 | 2 | | 1985 | 3 | 1 | 4 | | 1986 | 2 | 1 | 3 | | 1987 | 1 | 2 | 3 | | 1988 | 2 | 0 | 2 | | 1989 | 2 | 3 | 5 | | 1990 | 2 | 2 | 4 | | 1991 | 3 | 0 | 3 | | 1992 | 1 | 2 | 3 | | 1993 | 1 | 2 | 3 | | 1994 | 2 | 0 | 2 | | 1995 | 4 | 1 | 5 | | 1996 | 2 | 0 | 2 | | 1997 | 3 | 1 | 4 | | 1998 | 2 | 1 | 3 | | 1999 | 5 | 1 | 6 | | 2000 | 4 | 0 | 4 | | 2001 | 2 | 1 | 3 | | 2002 | 3 | 0 | 3 | | 2003 | 7 | 2 | 9 | | 2004 | 10 | 5 | 15 | | 2005 | 4 | 1 | 5 | | 2006 | 1 | 1 | 2 | | 2007 | 5 | 3 | 8 | | 2008 | 6 | 4 | 10 | | 2009 | 3 | 2 | 5 | | 2010 | 9 | 1 | 10 | | 2011 | 6 | 2 | 8 | | 2012 | 5 | 0 | 5 | | 2013 | 8 | 2 | 10 | | 2014 | 5 | 1 | 6 | | 2015 | 10 | 1 | 11 | | 2016 | 4 | 3 | 7 | | 2017 | 2 | 1 | 3 | | 2018 | 5 | 0 | 5 | | 2019 | 4 | 0 | 4 | | 2020 | 6 | 0 | 6 | | 2021 | 3 | 0 | 3 | | 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Abnormalities, Multiple" by people in Profiles.
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Grullon K, Ashi SA, Shea CR, Ruiz de Luzuriaga AM, Stein SL, Rosenblatt AE. Follicular keratosis of the face in pediatric patients of color. Pediatr Dermatol. 2022 Mar; 39(2):231-235.
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Mancini GMS, Smits DJ, Dekker J, Schot R, de Wit MCY, Lequin MH, Dremmen M, Brooks AS, van Ham T, Verheijen FW, Fornerod M, Dobyns WB, Wilke M. Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist. Eur J Paediatr Neurol. 2021 Nov; 35:27-34.
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Kalantari S, Carlston C, Alsaleh N, Abdel-Salam GMH, Alkuraya F, Kato M, Matsumoto N, Miyatake S, Yamamoto T, Fares-Taie L, Rozet JM, Chassaing N, Vincent-Delorme C, Kang-Bellin A, McWalter K, Bupp C, Palen E, Wagner MD, Niceta M, Cesario C, Milone R, Kaplan J, Wadman E, Dobyns WB, Filges I. Expanding the KIF4A-associated phenotype. Am J Med Genet A. 2021 12; 185(12):3728-3739.
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Kohli U, Jeevanandam V, Patel AR. Rare Variant of Shone Complex. Circ Cardiovasc Imaging. 2021 06; 14(6):e012317.
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Gileta AF, Helgeson ML, Leonard JMM, Pyle LC, Subramanian HP, Arndt K, Hawkes CP, Del Gaudio D. Further delineation of a recognizable type of syndromic short stature caused by biallelic SEMA3A loss-of-function variants. Am J Med Genet A. 2021 03; 185(3):889-893.
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Adam AP, Curry CJ, Hall JG, Keppler-Noreuil KM, Adam MP, Dobyns WB. Recurrent constellations of embryonic malformations re-conceptualized as an overlapping group of disorders with shared pathogenesis. Am J Med Genet A. 2020 11; 182(11):2646-2661.
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Andelman-Gur MM, Leventer RJ, Hujirat M, Ganos C, Yosovich K, Carmi N, Lev D, Nissenkorn A, Dobyns WB, Bhatia K, Lerman-Sagie T, Blumkin L. Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome? Am J Med Genet A. 2020 10; 182(10):2207-2213.
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Suresh S, Brewerton C, Plunkett B. Fetal Anomalies in a Pregnant Woman with a History of Hirschsprung Disease and a Tracheal Web. Neoreviews. 2020 07; 21(7):e489-e494.
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Unlu G, Qi X, Gamazon ER, Melville DB, Patel N, Rushing AR, Hashem M, Al-Faifi A, Chen R, Li B, Cox NJ, Alkuraya FS, Knapik EW. Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies. Nat Med. 2020 01; 26(1):98-109.
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Mak CCY, Doherty D, Lin AE, Vegas N, Cho MT, Viot G, Dimartino C, Weisfeld-Adams JD, Lessel D, Joss S, Li C, Gonzaga-Jauregui C, Zarate YA, Ehmke N, Horn D, Troyer C, Kant SG, Lee Y, Ishak GE, Leung G, Barone Pritchard A, Yang S, Bend EG, Filippini F, Roadhouse C, Lebrun N, Mehaffey MG, Martin PM, Apple B, Millan F, Puk O, Hoffer MJV, Henderson LB, McGowan R, Wentzensen IM, Pei S, Zahir FR, Yu M, Gibson WT, Seman A, Steeves M, Murrell JR, Luettgen S, Francisco E, Strom TM, Amlie-Wolf L, Kaindl AM, Wilson WG, Halbach S, Basel-Salmon L, Lev-El N, Denecke J, Vissers LELM, Radtke K, Chelly J, Zackai E, Friedman JM, Bamshad MJ, Nickerson DA. MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
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