Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
van Dongen, Jenny
Slagboom, P. Eline
Draisma, Harmen H. M.
Martin, Nicholas G.
and
Boomsma, Dorret I.
2012.
The continuing value of twin studies in the omics era.
Nature Reviews Genetics,
Vol. 13,
Issue. 9,
p.
640.
Charney, Evan
2012.
Humans, fruit flies, and automatons.
Behavioral and Brain Sciences,
Vol. 35,
Issue. 5,
p.
381.
Ketelaar, ME
Hofstra, RMW
and
Hayden, MR
2012.
What monozygotic twins discordant for phenotype illustrate about mechanisms influencing genetic forms of neurodegeneration.
Clinical Genetics,
Vol. 81,
Issue. 4,
p.
325.
Scheet, Paul
Ehli, Erik A.
Xiao, Xiangjun
van Beijsterveldt, Catharina E. M.
Abdellaoui, Abdel
Althoff, Robert R.
Hottenga, Jouke Jan
Willemsen, Gonneke
Nelson, Kelly A.
Huizenga, Patricia E.
Hu, Yueshan
Amos, Christopher I.
Bartels, Meike
Groen-Blokhuis, Maria M
de Geus, Eco JC
Hudziak, James J.
Davies, Gareth E.
and
Boomsma, Dorret I.
2012.
Twins, Tissue, and Time: An Assessment of SNPs and CNVs.
Twin Research and Human Genetics,
Vol. 15,
Issue. 6,
p.
737.
Bogdanos, Dimitrios P.
Smyk, Daniel S.
Rigopoulou, Eirini I.
Mytilinaiou, Maria G.
Heneghan, Michael A.
Selmi, Carlo
and
Eric Gershwin, M.
2012.
Twin studies in autoimmune disease: Genetics, gender and environment.
Journal of Autoimmunity,
Vol. 38,
Issue. 2-3,
p.
J156.
Painter, Jodie N.
Medland, Sarah J.
Montgomery, Grant W.
and
Hall, Judith G.
2013.
Emery and Rimoin's Principles and Practice of Medical Genetics.
p.
1.
Chen, Kristen
Chmait, Ramen H.
Vanderbilt, Douglas
Wu, Samuel
and
Randolph, Linda
2013.
Chimerism in monochorionic dizygotic twins: Case study and review.
American Journal of Medical Genetics Part A,
Vol. 161,
Issue. 7,
p.
1817.
Vlckova, Marketa
Hancarova, Miroslava
Drabova, Jana
Slamova, Zuzana
Koudova, Monika
Alanova, Renata
Mannik, Katrin
Kurg, Ants
and
Sedlacek, Zdenek
2014.
Monozygotic Twins with 17q21.31 Microdeletion Syndrome.
Twin Research and Human Genetics,
Vol. 17,
Issue. 5,
p.
405.
Chaiyasap, Pongsathorn
Kulawonganunchai, Supasak
Srichomthong, Chalurmpon
Tongsima, Sissades
Suphapeetiporn, Kanya
Shotelersuk, Vorasuk
and
Ballestar, Esteban
2014.
Whole Genome and Exome Sequencing of Monozygotic Twins with Trisomy 21, Discordant for a Congenital Heart Defect and Epilepsy.
PLoS ONE,
Vol. 9,
Issue. 6,
p.
e100191.
Pachman, Lauren M.
2015.
Neuromuscular Disorders of Infancy, Childhood, and Adolescence.
p.
834.
Brosens, Erwin
Snoek, K.G.
Veenma, D.
Eussen, H.
Tibboel, D.
and
Klein, A. de
2016.
Genome-Wide Association Studies.
p.
168.
Xu, Yuejuan
Li, Tingting
Pu, Tian
Cao, Ruixue
Long, Fei
Chen, Sun
Sun, Kun
and
Xu, Rang
2017.
Copy Number Variants and Exome Sequencing Analysis in Six Pairs of Chinese Monozygotic Twins Discordant for Congenital Heart Disease.
Twin Research and Human Genetics,
Vol. 20,
Issue. 6,
p.
521.
Chen, Fei
Li, Zhen
Li, Rong
and
Li, Yunlong
2018.
Whole‑genome sequencing of a monozygotic twin discordant for systemic lupus erythematosus.
Molecular Medicine Reports,
Stamouli, Sofia
Anderlid, Britt-Marie
Willfors, Charlotte
Thiruvahindrapuram, Bhooma
Wei, John
Berggren, Steve
Nordgren, Ann
Scherer, Stephen W.
Lichtenstein, Paul
Tammimies, Kristiina
and
Bölte, Sven
2018.
Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.
Twin Research and Human Genetics,
Vol. 21,
Issue. 1,
p.
1.
Umstad, Mark P.
Calais-Ferreira, Lucas
Scurrah, Katrina J.
Hall, Judith G.
and
Craig, Jeffrey M.
2019.
Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.
p.
387.
Grunert, Marcel
Appelt, Sandra
Grossfeld, Paul
and
Sperling, Silke R.
2020.
The Needle in the Haystack—Searching for Genetic and Epigenetic Differences in Monozygotic Twins Discordant for Tetralogy of Fallot.
Journal of Cardiovascular Development and Disease,
Vol. 7,
Issue. 4,
p.
55.
Rydzanicz, Małgorzata
Olszewski, Pawel
Kedra, Darek
Davies, Hanna
Filipowicz, Natalia
Bruhn‐Olszewska, Bozena
Cavalli, Marco
Szczałuba, Krzysztof
Młynek, Marlena
Machnicki, Marcin M.
Stawiński, Piotr
Kostrzewa, Grażyna
Krajewski, Paweł
Śladowski, Dariusz
Chrzanowska, Krystyna
Dumanski, Jan P.
and
Płoski, Rafał
2021.
Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins—Diagnostic implications.
Molecular Genetics & Genomic Medicine,
Vol. 9,
Issue. 1,
Rydzanicz, Małgorzata
Glinkowski, Wojciech
Walczak, Anna
Koppolu, Agnieszka
Kostrzewa, Grażyna
Gasperowicz, Piotr
Pollak, Agnieszka
Stawiński, Piotr
and
Płoski, Rafał
2022.
Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosis.
American Journal of Medical Genetics Part A,
Vol. 188,
Issue. 5,
p.
1482.
Rydzanicz, Małgorzata
Kuzniewska, Bozena
Magnowska, Marta
Wójtowicz, Tomasz
Stawikowska, Aleksandra
Hojka, Anna
Borsuk, Ewa
Meyza, Ksenia
Gewartowska, Olga
Gruchota, Jakub
Miłek, Jacek
Wardaszka, Patrycja
Chojnicka, Izabela
Kondrakiewicz, Ludwika
Dymkowska, Dorota
Puścian, Alicja
Knapska, Ewelina
Dziembowski, Andrzej
Płoski, Rafał
and
Dziembowska, Magdalena
2024.
Mutation in the mitochondrial chaperone TRAP1 leads to autism with more severe symptoms in males.
EMBO Molecular Medicine,