About: Chong Ae Kim

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) ഗവേഷക (ml) araştırmacı (tr) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
rdfs:label	김정애 (ko) Chong Ae Kim (en) Chong Ae Kim (es) Chong Ae Kim (nl) Chong Ae Kim (sl) Chong Ae Kim (ast)
skos:prefLabel	김정애 (ko) Chong Ae Kim (en) Chong Ae Kim (es) Chong Ae Kim (nl) Chong Ae Kim (sl) Chong Ae Kim (ast)
name	김정애 (ko) Chong Ae Kim (en) Chong Ae Kim (es) Chong Ae Kim (nl) Chong Ae Kim (sl) Chong Ae Kim (ast)
LinkedIn personal profile ID	wds:Q40388281-6a4f69f1-43c2-7fdd-7f12-9237c64aa920
LinkedIn personal profile ID	chong-ae-kim-862165b1
Scopus author ID	wds:Q40388281-1AEE282D-00D2-4E5A-8CBD-9BA7D321EC00
Scopus author ID	7409876947
given name	wds:Q40388281-0746a9dd-4a99-2f01-a9f6-4e9059d7e546
given name	Jeong-ae
instance of	wds:Q40388281-3AB73406-2435-41F6-B868-50AEB4A21FC5
instance of	Homo sapiens
Loop ID	wds:Q40388281-4d1e06a1-49ad-60b1-51c7-3fa8fd6b8617
Loop ID	1047103
Google Scholar author ID	wds:Q40388281-577bd71b-40ad-511c-bb09-41f5fe050ad4
Google Scholar author ID	59SEZFEAAAAJ
occupation	wds:Q40388281-CA25518F-5E92-4A17-88D1-C8DEE7EDCA75
employer	wds:Q40388281-4BDE3024-AB60-4D3C-9E33-CD4021D854B5
ethnic group	wds:Q40388281-06c6c1be-47fa-8012-e862-d20d5c896dad
sex or gender	wds:Q40388281-55f0379a-4fdc-87b2-1580-2f21d56e4553
VIAF ID	wds:Q40388281-BEADDCFA-A800-4E10-A4B8-E663EDE5EC09
family name	wds:Q40388281-63402e8b-48e8-ab18-cf12-c33e7a1131cb
WorldCat Identities ID (superseded)	wds:Q40388281-078148BF-A5B2-4C8D-92EA-7A354614AA55
VIAF ID	http://viaf.org/viaf/596150323826609972532
occupation	researcher
employer	Faculty of Medicine of the University of São Paulo
ethnic group	Korean Brazilians
sex or gender	female organism
VIAF ID	596150323826609972532
family name	Kim
WorldCat Identities ID (superseded)	viaf-596150323826609972532
ORCID iD	wds:Q40388281-10E7E1F0-514D-4FD4-B460-EE027B6757DF
Dimensions author ID	wds:Q40388281-20B44E72-B83F-489A-8F46-36B20C1BFFB3
ORCID iD	https://orcid.org/0000-0002-1754-1300
ORCID iD	0000-0002-1754-1300
Dimensions author ID	01224243631.11
ResearcherID	wds:Q40388281-62fd5402-41c7-74f6-12cb-f2276853f6f9
Publons author ID	wds:Q40388281-402d8917-4fe5-6c56-4053-745ce4c16475
ResearcherID	J-5769-2014
Publons author ID	2500471
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q40388281
is author of	Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans. Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome Report of a del22q11 in a patient with Mayer-Rokitansky-Küster-Hauser (MRKH) anomaly and exclusion ofWNT-4,RAR-gamma, andRXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women Prevalence of mutations in AGPAT2 among human lipodystrophies Echocardiographic study of paediatric patients with mucopolysaccharidosis Genomic imbalances associated with mullerian aplasia Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver-Russell syndrome. Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene in South American patients. Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation. Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Mutational Screening of FGFR1, CER1, and CDON in a Large Cohort of Trigonocephalic Patients A clinical study of 77 patients with mucopolysaccharidosis type II Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.

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