About: Iben Bache

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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) 研究者 (ja) araştırmacı (tr) дослідниця (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) hulumtuese (sq)
rdfs:label	Iben Bache (en) Iben Bache (es) Iben Bache (nl) Iben Bache (sl)
skos:prefLabel	Iben Bache (en) Iben Bache (es) Iben Bache (nl) Iben Bache (sl)
name	Iben Bache (en) Iben Bache (es) Iben Bache (nl) Iben Bache (sl)
Scopus author ID	wds:Q55692610-F057E7A9-D030-4387-8CBE-10EA73D931C0
Scopus author ID	12243546800
given name	wds:Q55692610-F7FF601F-0863-4137-A1AD-F3EEFABD5FCF
given name	Iben
instance of	wds:Q55692610-B96A8CE0-A7AE-4EC2-A9EC-60E6DFB42BF0
instance of	Homo sapiens
occupation	wds:Q55692610-05D2D0EB-C50B-49A5-90D1-98B08C7B042D
employer	wds:Q55692610-F28AB7F6-594B-4D6A-B170-1A297CE98E41
sex or gender	wds:Q55692610-00EB59E5-CF9E-4DBF-8D37-979D48A6C35B
family name	wds:Q55692610-B44FDFE8-5E6C-4B93-B790-0B936E61A0A0
official website	wds:Q55692610-52BCDE7A-3188-4C34-847A-81517F573C9F
occupation	researcher
employer	University of Copenhagen
sex or gender	female organism
family name	Bache
official website	https://curis.ku.dk/portal/en/persons/iben-bache(bb160617-68f4-4c3a-aac6-4788391d391e).html
ORCID iD	wds:Q55692610-72E5CE60-CE28-49E8-A08F-CF67609CD9C2
ORCID iD	https://orcid.org/0000-0001-7562-8546
ORCID iD	0000-0001-7562-8546
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55692610
is author of	Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features Autoimmune diseases in women with Turner's Syndrome Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1 Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder. Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases Haploinsufficiency of TAB2 causes congenital heart defects in humans De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway Multigenic truncation of the semaphorin-plexin pathway by a germline chromothriptic rearrangement associated with Moebius syndrome Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes A shared somatic translocation involving CUX1 in monozygotic twins as an early driver of AMKL in Down syndrome Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity. Simulation based virtual learning environment in medical genetics counseling: an example of bridging the gap between theory and practice in medical education. 3q27.3 microdeletional syndrome: a recognisable clinical entity associating dysmorphic features, marfanoid habitus, intellectual disability and psychosis with mood disorder. Rare novel variants in the ZIC3 gene cause X-linked heterotaxy Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development von Hippel-Lindau development in children and adolescents 17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature. Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy Re-Examination of Danish Carriers of Balanced Chromosomal Inversions A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia. Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects Haploinsufficiency of ARHGAP42 is associated with hypertension
is author of	wds:Q58612547-30273974-4847-4FF5-8C6C-15FA74B93F7C wds:Q91592913-25A84B60-E634-4E78-8868-B11D4EAAB311 wds:Q90009121-8B1D59B8-41DC-4951-8F3F-E5BD5D06DF9D wds:Q39608817-D4EB2D60-FAD4-4E43-B0D2-AF65B2428CA5 wds:Q36550132-3592FF15-40B6-42D6-8CE9-15D494960B79 wds:Q39648328-8416F938-0A4E-456B-8D71-26061D241677 wds:Q48844602-63AAE4B1-C09A-4F4A-BED4-43BA1C4FB0C8 wds:Q58060845-A9429BCB-5620-48F2-92B6-71F14CC216E7 wds:Q58612571-3C132183-FFB2-4A1A-8E5A-97D47F12734C wds:Q61825862-ECD17F4A-F70F-4EE3-BD24-F60D7DEF5F05 wds:Q57422845-BBCA9491-B30B-429E-8D71-167EE0EB28E8 wds:Q57422870-7BE6FCB2-413D-4A85-AA09-1ABA30E47CB6 wds:Q91029743-8A161285-A64F-4E50-B775-B6E0BF804115 wds:Q36403943-2A75B42F-08B2-499E-8E71-297FA0DEA20B wds:Q54743332-BF082445-FB93-49EB-8712-375F1D22C7E1 wds:Q50310919-29689894-FACF-4CE8-9F65-0BA308A64844 wds:Q58612559-292E25B7-A399-4E38-9155-F5A376F2AF0E wds:Q24314581-5C0B4E07-7DE2-4696-8BE7-732FAB8B94CA wds:Q88391523-0F8934E9-288B-4927-A4EA-4EA1CBABEC61 wds:Q36297753-A4C6D66A-AB0C-488E-B432-64EA8EA08654 wds:Q58612720-0C2FC9E7-833B-4787-9C03-45E9E6E469B2 wds:Q92565055-79645180-63B6-4302-976B-1BED049393FC wds:Q27308756-F3C86F83-4442-4EEF-B404-8D68662B3838 wds:Q52127974-0B061879-CE77-4A21-B354-086611E2F502

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