Rare variants analyses suggest novel cleft genes in the African population

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Rare variants analyses suggest novel cleft genes in the African population ; volume:14 ; number:1 ; day:20 ; month:6 ; year:2024 ; pages:1-10 ; date:12.2024
Scientific reports ; 14, Heft 1 (20.6.2024), 1-10, 12.2024

Creator: Alade, Azeez
Mossey, Peter
Awotoye, Waheed
Busch, Tamara
Oladayo, Abimbola M.
Aladenika, Emmanuel
Olujitan, Mojisola
Wentworth, Emma
Anand, Deepti
Naicker, Thirona
Gowans, Lord J. J.
Eshete, Mekonen A.
Adeyemo, Wasiu L.
Zeng, Erliang
Otterloo, Eric Van
O’Rorke, Michael
Adeyemo, Adebowale
Murray, Jeffrey C.
Cotney, Justin
Lachke, Salil A.
Romitti, Paul
Butali, Azeez

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-024-65151-9

URN: urn:nbn:de:101:1-2409160920319.495888268193

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:25 AM CEST

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Associated

Alade, Azeez
Mossey, Peter
Awotoye, Waheed
Busch, Tamara
Oladayo, Abimbola M.
Aladenika, Emmanuel
Olujitan, Mojisola
Wentworth, Emma
Anand, Deepti
Naicker, Thirona
Gowans, Lord J. J.
Eshete, Mekonen A.
Adeyemo, Wasiu L.
Zeng, Erliang
Otterloo, Eric Van
O’Rorke, Michael
Adeyemo, Adebowale
Murray, Jeffrey C.
Cotney, Justin
Lachke, Salil A.
Romitti, Paul
Butali, Azeez
SpringerLink (Online service)

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Rare variants analyses suggest novel cleft genes in the African population

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Other Objects (12)

Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene

Repair of bilateral cleft lip and its variants

Repair of bilateral cleft lip and its variants

Pan-cancer analyses suggest kindlin-associated global mechanochemical alterations

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Cleft palate: a rare complication following esophageal stent implantation

SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients

Complete cleft of the upper limb: A very rare anomaly

Complete cleft of the upper limb: A very rare anomaly

Roberts-SC syndrome, a rare syndrome and cleft palate repair

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Functional analyses of rare germline BRCA1 variants by transcriptional activation and homologous recombination repair assays

Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene

Repair of bilateral cleft lip and its variants

Repair of bilateral cleft lip and its variants

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Cleft palate: a rare complication following esophageal stent implantation

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Complete cleft of the upper limb: A very rare anomaly

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Roberts-SC syndrome, a rare syndrome and cleft palate repair

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Complete cleft of the upper limb: A very rare anomaly

Roberts-SC syndrome, a rare syndrome and cleft palate repair

Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores

Functional analyses of rare germline BRCA1 variants by transcriptional activation and homologous recombination repair assays

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