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The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative.

• Authors : Calkins ME; University of Pennsylvania, Department of Psychiatry, Neuropsychiatry Section, Perelman School of Medicine, PA, United States.; Merikangas KR

Subjects: Databases, Factual* ; Genotype* ; Phenotype*

• Source: Journal of child psychology and psychiatry, and allied disciplines [J Child Psychol Psychiatry] 2015 Dec; Vol. 56 (12), pp. 1356-1369. Date of Electronic Publication: 2015 Apr 08.Publisher: Blackwell Publishers Country of Publication: England NLM ID: 0375361 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Deep Phenotyping in 1p36 Deletion Syndrome

• Authors : Youngkyu Shim; Young Jun Go; Soo Yeon Kim

Subjects: chromosome 1p36 deletion syndrome; phenotype; genotype

• Source: Annals of Child Neurology, Vol 28, Iss 4, Pp 131-137 (2020)

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Deep Phenotyping in 1p36 Deletion Syndrome.

• Authors : Shim, Youngkyu¹; Go, Young Jun¹; Kim, Soo Yeon^1,2

• Source: Annals of Child Neurology. Oct2020, Vol. 28 Issue 4, p131-137. 7p.

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RBP3-retinopathy - inherited high myopia and retinal dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping

• Authors : Georgiou, Michalis; Fujinami, Kaoru; Robson, Anthony G

Subjects: RBP3 retinopathy; RBP3; retinal dystrophy

• Source: American Journal of Ophthalmology (2023) (In press).

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X-linked Retinoschisis: Deep Phenotyping and Genetic Characterization

• Authors : Georgiou, M; Finocchio, L; Fujinami, K

Subjects: Fundus Autofluorescence; Optical Coherence Tomography; RS1

• Source: Ophthalmology , 129 (5) pp. 542-551. (2022)

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Deep Phenotyping in KCNV2-associated Retinopathy

• Authors : Cabral De Guimarães, Thales Antônio;

Subjects: KCNV2; Cone rod dystrophy; IRD

• Source: Doctoral thesis, UCL (University College London).

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The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative

• Authors : Rosetta M. Chiavacci; Tyler M. Moore; Theodore D. Satterthwaite

Subjects: Adult; Male; medicine.medical_specialty

• Source: Journal of Child Psychology and Psychiatry. 56:1356-1369

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Phenotype-Based Genetic Association Studies (PGAS)—Towards Understanding the Contribution of Common Genetic Variants to Schizophrenia Subphenotypes

• Authors : Hannelore Ehrenreich; Klaus-Armin Nave

Subjects: mental disease; diagnosis; classification systemsagris

• Source: Genes; Volume 5; Issue 1; Pages: 97-105

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Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes.

• Authors : Magrinelli, Francesca^1,2 (AUTHOR) ; Balint, Bettina^1,3 (AUTHOR); Bhatia, Kailash P.¹ (AUTHOR)

• Source: Movement Disorders Clinical Practice. Apr2021, Vol. 8 Issue 3, p299-310. 12p.

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Challenges in Clinicogenetic Correlations: One Phenotype – Many Genes.

• Authors : Gannamani, Rahul^1,2,3 (AUTHOR); Veen, Sterre^1,3 (AUTHOR); Egmond, Martje^1,3 (AUTHOR)

• Source: Movement Disorders Clinical Practice. Apr2021, Vol. 8 Issue 3, p311-321. 11p.

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