| Year |
Citation |
Score |
| 2020 |
Seven M, Shah LL, Yazici H, Daack-Hirsch S. From Probands to Relatives: Communication of Genetic Risk for Hereditary Breast-Ovarian Cancer and Its Influence on Subsequent Testing. Cancer Nursing. PMID 32804756 DOI: 10.1097/Ncc.0000000000000876 |
0.322 |
|
| 2020 |
Seven M, Shah LL, Daack-Hirsch S, Yazici H. Experiences of BRCA1/2 Gene Mutation-Positive Women With Cancer in Communicating Genetic Risk to Their Relatives. Cancer Nursing. PMID 32022782 DOI: 10.1097/Ncc.0000000000000796 |
0.325 |
|
| 2018 |
Shah LL, Daack-Hirsch S, Ersig AL, Paik A, Ahmad F, Williams J. Family Relationships Associated With Communication and Testing for Inherited Cardiac Conditions. Western Journal of Nursing Research. 193945918817039. PMID 30539690 DOI: 10.1177/0193945918817039 |
0.332 |
|
| 2018 |
Shah LL, Daack-Hirsch S. Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review. Journal of Genetic Counseling. PMID 29492742 DOI: 10.1007/S10897-018-0225-9 |
0.308 |
|
| 2016 |
Abad PJ, Anonuevo CA, Daack-Hirsch S, Abad LR, Padilla CD, Laurino MY. Communication about Congenital Adrenal Hyperplasia: Perspective of Filipino Families. Journal of Genetic Counseling. PMID 27832511 DOI: 10.1007/S10897-016-0043-X |
0.351 |
|
| 2016 |
Daack-Hirsch S. The International Society of Nurses in Genetics (ISONG) 2015 World Congress: Epigenetics Across the Life Span. Biological Research For Nursing. 18: 125-126. PMID 26912580 DOI: 10.1177/1099800416630133 |
0.319 |
|
| 2016 |
Williams JK, Tripp-Reimer T, Daack-Hirsch S, DeBerg J. Five-Year Bibliometric Review of Genomic Nursing Science Research. Journal of Nursing Scholarship : An Official Publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau. PMID 26836310 DOI: 10.1111/Jnu.12196 |
0.312 |
|
| 2013 |
Daack-Hirsch S, Jackson B, Belchez CA, Elder BL, Hurley R, Kerr P, Nissen MK. Integrating genetics and genomics into nursing curricula: you can do it too! Nursing Clinics of North America. 48: 661-669. PMID 24295193 DOI: 10.1016/J.Cnur.2013.08.005 |
0.312 |
|
| 2013 |
Williams JK, Daack-Hirsch S, Driessnack M, Downing NR, Simon C. The importance of patient engagement. Genetic Testing and Molecular Biomarkers. 17: 649. PMID 23941073 DOI: 10.1089/Gtmb.2013.0346 |
0.315 |
|
| 2013 |
Daack-Hirsch S, Driessnack M, Hanish A, Johnson VA, Shah LL, Simon CM, Williams JK. 'Information is information': a public perspective on incidental findings in clinical and research genome-based testing. Clinical Genetics. 84: 11-8. PMID 23590238 DOI: 10.1111/Cge.12167 |
0.303 |
|
| 2013 |
Driessnack M, Daack-Hirsch S, Downing N, Hanish A, Shah LL, Alasagheirin M, Simon CM, Williams JK. The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practice. Journal of Community Genetics. 4: 435-44. PMID 23572417 DOI: 10.1007/S12687-013-0145-1 |
0.302 |
|
| 2013 |
Brandt DS, Shinkunas L, Hillis SL, Daack-Hirsch SE, Driessnack M, Downing NR, Liu MF, Shah LL, Williams JK, Simon CM. A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs. Journal of Genetic Counseling. 22: 544-53. PMID 23547023 DOI: 10.1007/S10897-013-9583-5 |
0.361 |
|
| 2013 |
Daack-Hirsch S, Holtzer C, Cunniff C. Parental Perspectives on the Diagnostic Process for Duchenne and Becker Muscular Dystrophy. American Journal of Medical Genetics Part A. 161: 687-695. PMID 23494880 DOI: 10.1002/Ajmg.A.35810 |
0.31 |
|
| 2013 |
Downing NR, Williams JK, Daack-Hirsch S, Driessnack M, Simon CM. Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting. Patient Education and Counseling. 90: 133-8. PMID 23068909 DOI: 10.1016/J.Pec.2012.09.010 |
0.319 |
|
| 2011 |
Simon CM, Williams JK, Shinkunas L, Brandt D, Daack-Hirsch S, Driessnack M. Informed consent and genomic incidental findings: IRB chair perspectives. Journal of Empirical Research On Human Research Ethics : Jerhre. 6: 53-67. PMID 22228060 DOI: 10.1525/Jer.2011.6.4.53 |
0.305 |
|
| 2011 |
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC. Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 85-92. PMID 21319277 DOI: 10.1002/Bdra.20747 |
0.313 |
|
| 2011 |
Petrin AL, Daack-Hirsch S, L'Heureux J, Murray JC. A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 48: 222-30. PMID 20500065 DOI: 10.1597/09-149 |
0.317 |
|
| 2010 |
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC. Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. Plos One. 5: e11493. PMID 20634891 DOI: 10.1371/Journal.Pone.0011493 |
0.329 |
|
| 2009 |
Marazita ML, Lidral AC, Murray JC, Field LL, Maher BS, Goldstein McHenry T, Cooper ME, Govil M, Daack-Hirsch S, Riley B, Jugessur A, Felix T, Morene L, Mansilla MA, Vieira AR, et al. Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. Human Heredity. 68: 151-70. PMID 19521098 DOI: 10.1159/000224636 |
0.353 |
|
| 2009 |
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Trung TN, Bille C, Lidral AC, Murray JC. Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia. Plos One. 4: e5385. PMID 19401770 DOI: 10.1371/Journal.Pone.0005385 |
0.353 |
|
| 2009 |
de Lima RL, Hoper SA, Ghassibe M, Cooper ME, Rorick NK, Kondo S, Katz L, Marazita ML, Compton J, Bale S, Hehr U, Dixon MJ, Daack-Hirsch S, Boute O, Bayet B, et al. Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 241-7. PMID 19282774 DOI: 10.1097/Gim.0B013E318197A49A |
0.316 |
|
| 2009 |
Suzuki S, Marazita ML, Cooper ME, Miwa N, Hing A, Jugessur A, Natsume N, Shimozato K, Ohbayashi N, Suzuki Y, Niimi T, Minami K, Yamamoto M, Altannamar TJ, Erkhembaatar T, ... ... Daack-Hirsch S, et al. Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. American Journal of Human Genetics. 84: 406-11. PMID 19249007 DOI: 10.1016/J.Ajhg.2009.02.002 |
0.341 |
|
| 2008 |
Vieira AR, McHenry TG, Daack-Hirsch S, Murray JC, Marazita ML. A genome wide linkage scan for cleft lip and palate and dental anomalies. American Journal of Medical Genetics Part A. 146: 1406-1413. PMID 18442096 DOI: 10.1002/Ajmg.A.32295 |
0.379 |
|
| 2007 |
Kimani JW, Shi M, Daack-Hirsch S, Christensen K, Moretti-Ferreira D, Marazita ML, Field LL, Canady JW, Murray JC. X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate. American Journal of Medical Genetics Part A. 143: 3267-3272. PMID 18000982 DOI: 10.1002/Ajmg.A.32098 |
0.307 |
|
| 2007 |
Riley BM, Schultz RE, Cooper ME, Goldstein-McHenry T, Daack-Hirsch S, Lee KT, Dragan E, Vieira AR, Lidral AC, Marazita ML, Murray JC. A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23 American Journal of Medical Genetics Part A. 143: 846-852. PMID 17366557 DOI: 10.1002/Ajmg.A.31673 |
0.397 |
|
| 2005 |
Vieira AR, Avila JR, Daack-Hirsch S, Dragan E, Félix TM, Rahimov F, Harrington J, Schultz RR, Watanabe Y, Johnson M, Fang J, O'Brien SE, Orioli IM, Castilla EE, Fitzpatrick DR, et al. Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. Plos Genetics. 1: e64. PMID 16327884 DOI: 10.1371/Journal.Pgen.0010064 |
0.378 |
|
| 2004 |
Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, et al. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. The New England Journal of Medicine. 351: 769-80. PMID 15317890 DOI: 10.1056/Nejmoa032909 |
0.408 |
|
| 2004 |
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, et al. Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. American Journal of Human Genetics. 75: 161-73. PMID 15185170 DOI: 10.1086/422475 |
0.372 |
|
| 2004 |
Schultz RE, Cooper ME, Daack-Hirsch S, Shi M, Nepomucena B, Graf KA, O'Brien EK, O'Brien SE, Marazita ML, Murray JC. Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. American Journal of Medical Genetics Part A. 125: 17-22. PMID 14755461 DOI: 10.1002/Ajmg.A.20424 |
0.371 |
|
| 2003 |
Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, et al. Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate Journal of Medical Genetics. 40: 399-407. PMID 12807959 DOI: 10.1136/Jmg.40.6.399 |
0.341 |
|
| 2002 |
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, et al. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature Genetics. 32: 285-9. PMID 12219090 DOI: 10.1038/Ng985 |
0.331 |
|
| 2000 |
Roeder ER, Khan-Catts ZA, Fisher JH, Daack-Hirsch S, Murray JC, Curry CJR. Oral clefting, cartilaginous auricular malformations and other anomalies: A provisionally unique autosomal dominant syndrome Genetics in Medicine. 2: 85-85. DOI: 10.1097/00125817-200001000-00123 |
0.344 |
|
| 1998 |
Yoshiura Ki, Machida J, Daack-Hirsch S, Patil SR, Ashworth LK, Hecht JT, Murray JC. Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate Genomics. 54: 231-240. PMID 9828125 DOI: 10.1006/Geno.1998.5577 |
0.337 |
|
| 1998 |
Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. American Journal of Human Genetics. 63: 557-68. PMID 9683588 DOI: 10.1086/301956 |
0.364 |
|
| 1998 |
Semina EV, Ferrell RE, Mintz-Hittner HA, Bitoun P, Alward WLM, Reiter RS, Funkhauser C, Daack-Hirsch S, Murray JC. A novel homeobox gene PITX3 is mutated in families with autosomal- dominant cataracts and ASMD Nature Genetics. 19: 167-170. PMID 9620774 DOI: 10.1038/527 |
0.337 |
|
| 1997 |
Murray JC, Daack-Hirsch S, Buetow KH, Munger R, Espina L, Paglinawan N, Villanueva E, Rary J, Magee K, Magee W. Clinical and epidemiologic studies of cleft lip and palate in the Philippines Cleft Palate-Craniofacial Journal. 34: 7-10. PMID 9003905 DOI: 10.1597/1545-1569_1997_034_0007_Caesoc_2.3.Co_2 |
0.356 |
|
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