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1
von Waheeda A. Hossain ; Merlin G. Butler
Frontiers in Genetics, Vol 17 (2026)
Schlagworte: addiction and alcoholism genes; addiction and related behavior; biological processes; genetic mechanisms; molecular functions; pathways and gene–disease associations; Genetics; QH426-470
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2
von Shokouh Shahrokhi ; Emma K. Baker ; Michael See ; et al.
Scientific Reports, Vol 16, Iss 1, Pp 1-11 (2025)
Schlagworte: RPS18; Prader-Willi syndrome; Behavioral issues; Intellectual functioning; Brain transcriptomics; Medicine; Science
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3
von Merlin G. Butler
International Journal of Molecular Sciences ; Volume 27 ; Issue 3 ; Pages: 1270
Schlagworte: Prader–Willi and Angelman syndromes; review; clinical presentations; laboratory testing and genetic counseling; genomic imprinting; candidate or causative genes and defects; molecular genetic classes of chromosome 15q11-q13 region; integrated genetic analysis of predicted gene and protein interactions; clinical trials and treatment strategies
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4
von Lucas Francis ; Merlin G. Butler
Current Issues in Molecular Biology, Vol 47, Iss 12, p 1007 (2025)
Schlagworte: glucagon-like peptide-1 (GLP1) receptor (GLP1R) gene; GLP1R agonist; gene-gene or protein interactions, biological processes, functions, pathways and associated diseases; obesity; weight loss; insulin; Biology (General); QH301-705.5
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5
von Butler, Merlin G. ; Butler, Merlin G., editor ; Lee, Phillip D. K., editor ; et al.
Management of Prader-Willi Syndrome. :499-527
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6
von Stamm, Stefan ; Butler, Merlin G. ; Butler, Merlin G., editor ; et al.
Management of Prader-Willi Syndrome. :51-73
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7
von Merlin G. Butler ; Spencer Silvey ; Harold J. P. van Bosse
Genes ; Volume 16 ; Issue 12 ; Pages: 1436
Schlagworte: barriers and limitations; clinical trials and experiences; rare diseases; Prader-Willi syndrome; KCNJ11 gene and protein interactions; functions; and mechanisms; diazoxide choline
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8
von Duis, Jessica ; Butler, Merlin G. ; Butler, Merlin G., editor ; et al.
Management of Prader-Willi Syndrome. :93-120
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9
von Butler, Merlin G. ; Thompson, Travis ; Butler, Merlin G., editor ; et al.
Management of Prader-Willi Syndrome. :3-50
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10
von Spencer Silvey ; Scott Lovell ; Merlin G. Butler
Genes ; Volume 16 ; Issue 9 ; Pages: 1063
Schlagworte: RNA polymerase I disorders; STRING genetic mechanisms; functions; pathways; cellular components; human phenotypes; and ribosomopathies; craniofacial; cardiac; skeletal; and neurodevelopmental anomalies; protein profiling; genetic and clinical syndromic correlations
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11
von Ann C. Genovese ; Merlin G. Butler
Genes ; Volume 16 ; Issue 9 ; Pages: 1061
Schlagworte: PTEN gene; genetic functions and mechanisms; protein interactions; autism; ASD; neurodevelopment; macrocephaly; abnormal CSF dynamics
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12
von Ann C. Genovese ; Merlin G. Butler
Genes ; Volume 16 ; Issue 2 ; Pages: 149
Schlagworte: fragile X syndrome; lifespan; genetics; neurodevelopmental; behavioral; psychiatric
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13
von Waheeda A. Hossain ; Caroline St. Peter ; Scott Lovell ; et al.
International Journal of Molecular Sciences ; Volume 26 ; Issue 3 ; Pages: 1307
Schlagworte: Mowat–Wilson syndrome; neurodevelopmental disorder; ZEB2 gene variants; protein domains and non-domain regions; multi-system organ development; genotype–phenotype relationships
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14
von Butler, Merlin G. ; Pfaff, Donald W., editor ; Volkow, Nora D., editor ; et al.
Neuroscience in the 21st Century : From Basic to Clinical. :3563-3603
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15
von Butler, Merlin G. ; Victor, A. Kaitlyn ; Reiter, Lawrence T.
Clinical Autonomic Research: Official journal of the American Autonomic Society and the European Federation of Autonomic Societies. 33(3):281-286
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16
von Veatch, Olivia J. ; Malow, Beth A. ; Lee, Hye-Seung ; et al.
In Pediatric Neurology October 2021 123:30-37
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17
von Angulo, Moris A. ; Butler, Merlin G. ; Hossain, Waheeda A. ; et al.
Journal of Pediatric Endocrinology and Metabolism. 35(6):733-740
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18
von Olivia J. Veatch ; Jacob Steinle ; Waheeda A. Hossain ; et al.
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-14 (2022)
Schlagworte: Heritable connective tissue disorders; Ehlers–Danlos syndrome; Next-generation sequencing; Phenotype-genotype relationships; Gene variants; Latent class analysis; Internal medicine; RC31-1245; Genetics; QH426-470
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19
von Ann C. Genovese ; Merlin G. Butler
Brain Sciences ; Volume 14 ; Issue 4 ; Pages: 343
Schlagworte: autism spectrum disorder; syndromic autism; gene; chromosome; syndromes; neurodevelopment; behavior; psychology; psychiatry
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20
von Caroline St. Peter ; Waheeda A. Hossain ; Scott Lovell ; et al.
International Journal of Molecular Sciences, Vol 25, Iss 5, p 2838 (2024)
Schlagworte: Mowat–Wilson syndrome (MWS); case report; review; ZEB2 gene variants; ZEB2 protein domains and defects; ZEB2 functional molecular interactions; Biology (General); QH301-705.5; Chemistry; QD1-999
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21
von Adams, David R. ; Aday, Aaron ; Alejandro, Mercedes E. ; et al.
In The American Journal of Human Genetics 7 March 2019 104(3):422-438
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22
von Wang, Yu-Ping ; Gunampally, Maheswar ; Chen, Jie ; et al.
2007 IEEE International Workshop on Genomic Signal Processing and Statistics Genomic Signal Processing and Statistics, 2007. GENSIPS 2007. IEEE International Workshop on. :1-4 Jun, 2007
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23
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24
von Ann Genovese ; Merlin G. Butler
Genes ; Volume 14 ; Issue 3 ; Pages: 677
Schlagworte: autism spectrum disorder; behavior; genetic defects and associations; medical conditions; pharmacogenetics; psychiatry
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25
von Francis, Lucas ; Butler, Merlin G.
Current Issues in Molecular Biology. Dec2025, Vol. 47 Issue 12, p1007. 17p.
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