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Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.
Published in:
Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-15885-1
By:
- Awotoye, Waheed;
- Mossey, Peter A.;
- Hetmanski, Jacqueline B.;
- Gowans, Lord J. J.;
- Eshete, Mekonen A.;
- Adeyemo, Wasiu L.;
- Alade, Azeez;
- Zeng, Erliang;
- Adamson, Olawale;
- Naicker, Thirona;
- Anand, Deepti;
- Adeleke, Chinyere;
- Busch, Tamara;
- Li, Mary;
- Petrin, Aline;
- Aregbesola, Babatunde S.;
- Braimah, Ramat O.;
- Oginni, Fadekemi O.;
- Oladele, Ayodeji O.;
- Oladayo, Abimbola
Publication type:
Article
Replication of Genome Wide Association Identified Candidate Genes Confirm the Role of Common and Rare Variants in PAX 7 and VAX 1 in the Etiology of Nonsyndromic CL(P).
Published in:
American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 965, doi. 10.1002/ajmg.a.35749
By:
- Butali, Azeez;
- Suzuki, Satoshi;
- Cooper, Margaret E.;
- Mansilla, Adela M.;
- Cuenco, Karen;
- Leslie, Elizabeth J.;
- Suzuki, Yasushi;
- Niimi, Teruyuki;
- Yamamoto, Masahiko;
- Ayanga, Gongorjav;
- Erkhembaatar, Tudevdorj;
- Furukawa, Hiroo;
- Fujiwawa, Kumiko;
- Imura, Hideto;
- Petrin, Aline L.;
- Natsume, Nagato;
- Beaty, Terri H.;
- Marazita, Mary L.;
- Murray, Jeffery C.
Publication type:
Article
Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome.
Published in:
American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 8, p. 2003, doi. 10.1002/ajmg.a.35454
By:
- Kokitsu-Nakata, Nancy Mizue;
- Petrin, Aline Lourenço;
- Heard, Jason Paul;
- Vendramini-Pittoli, Siulan;
- Henkle, Laura E;
- dos Santos, Daniela Vera Cruz;
- Murray, Jeffrey Clark;
- Richieri-Costa, Antonio
Publication type:
Article
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.
Published in:
Cleft Palate Craniofacial Journal, 2024, v. 61, n. 4, p. 697, doi. 10.1177/10556656221135926
By:
- Awotoye, Waheed;
- Mossey, Peter A;
- Hetmanski, Jacqueline B;
- Gowans, Lord J J;
- Eshete, Mekonen A;
- Adeyemo, Wasiu L;
- Alade, Azeez;
- Zeng, Erliang;
- Adamson, Olawale;
- James, Olutayo;
- Fashina, Azeez;
- Ogunlewe, Modupe O;
- Naicker, Thirona;
- Adeleke, Chinyere;
- Busch, Tamara;
- Li, Mary;
- Petrin, Aline;
- Oladayo, Abimbola;
- Kayali, Sami;
- Olotu, Joy
Publication type:
Article
Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P).
Published in:
Cleft Palate Craniofacial Journal, 2022, v. 59, n. 7, p. 841, doi. 10.1177/10556656211036316
By:
- Gowans, Lord J. J.;
- Comnick, Carissa L.;
- Mossey, Peter A.;
- Eshete, Mekonen A.;
- Adeyemo, Wasiu L.;
- Naicker, Thirona;
- Awotoye, Waheed A.;
- Petrin, Aline;
- Adeleke, Chinyere;
- Donkor, Peter;
- Busch, Tamara D.;
- James, Olutayo;
- Ogunlewe, Mobolanle O.;
- Li, Mary;
- Olotu, Joy;
- Hassan, Mohaned;
- Adeniyan, Oluwole A.;
- Obiri-Yeboah, Solomon;
- Arthur, Fareed K. N.;
- Agbenorku, Pius
Publication type:
Article
A Case of 3q29 Microdeletion Syndrome Involving Oral Cleft Inherited From a Nonaffected Mosaic Parent: Molecular Analysis and Ethical Implications.
Published in:
Cleft Palate Craniofacial Journal, 2011, v. 48, n. 2, p. 222, doi. 10.1597/09-149
By:
- Petrin, Aline L.;
- Daack-Hirsch, Sandra;
- L'Heureux, Jamie;
- Murray, Jeffrey C.
Publication type:
Article
Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.
Published in:
Birth Defects Research, 2017, v. 109, n. 1, p. 27, doi. 10.1002/bdra.23596
By:
- Liu, Huan;
- Busch, Tamara;
- Eliason, Steven;
- Anand, Deepti;
- Bullard, Steven;
- Gowans, Lord J.J;
- Nidey, Nichole;
- Petrin, Aline;
- Augustine-Akpan, Eno-Abasi;
- Saadi, Irfan;
- Dunnwald, Martine;
- Lachke, Salil A.;
- Zhu, Ying;
- Adeyemo, Adebowale;
- Amendt, Brad;
- Roscioli, Tony;
- Cornell, Robert;
- Murray, Jeffrey;
- Butali, Azeez
Publication type:
Article
Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans.
Published in:
Genetics, 2018, v. 208, n. 1, p. 283, doi. 10.1534/genetics.117.300535
By:
- Lansdon, Lisa A.;
- Darbro, Benjamin W.;
- Petrin, Aline L.;
- Hulstrand, Alissa M.;
- Standley, Jennifer M.;
- Brouillette, Rachel B.;
- Long, Abby;
- Mansilla, M. Adela;
- Cornell, Robert A.;
- Murray, Jeffrey C.;
- Houston, Douglas W.;
- Manak, J. Robert
Publication type:
Article
Monozygotic twins with variable expression of Van der Woude Syndrome.
Published in:
American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 8, p. 2008, doi. 10.1002/ajmg.a.34022
By:
- Jobling, Rebekah;
- Ferrier, Raechel A.;
- McLeod, Ross;
- Petrin, Aline Lourenco;
- Murray, Jeffrey C.;
- Thomas, Mary Ann
Publication type:
Article
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
Published in:
Genetic Epidemiology, 2017, v. 41, n. 8, p. 887, doi. 10.1002/gepi.22090
By:
- Carlson, Jenna C.;
- Standley, Jennifer;
- Petrin, Aline;
- Shaffer, John R.;
- Butali, Azeez;
- Buxó, Carmen J.;
- Castilla, Eduardo;
- Christensen, Kaare;
- Deleyiannis, Frederic W.‐D.;
- Hecht, Jacqueline T.;
- Field, L. Leigh;
- Garidkhuu, Ariuntuul;
- Moreno Uribe, Lina M.;
- Nagato, Natsume;
- Orioli, Ieda M.;
- Padilla, Carmencita;
- Poletta, Fernando;
- Suzuki, Satoshi;
- Vieira, Alexandre R.;
- Wehby, George L.
Publication type:
Article

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