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Sandra Daack‐Hirsch

University of Iowa

33H指数
100论文数
6.0K被引数
收录论文 18
发表时间
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The impact of congenital heart disease on somatic growth: a monozygotic twin study先天性心脏病对体格发育的影响:一项单卵双胞胎研究
err2025-11-18
err0
errOAAI
errLee, J. H.; Yun, T. J.; Kwon, S. J.; Troy, Z.; Marshall, T. A.; Buck, H. G.; Mulder, P. J.; Daack-Hirsch, S.
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Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes
err2023-01-01
err6
errOAAI
errLansdon, Lisa A.; Dickinson, Amanda; Arlis, Sydney; Liu, Huan; Hlas, Arman; Hahn, Alyssa; Bonde, Greg; Long, Abby; Standley, Jennifer; Tyryshkina, Anastasia; Wehby, George; Lee, Nanette R.; Daack-Hirsch, Sandra; Mohlke, Karen; Girirajan, Santhosh; Darbro, Benjamin W.; Cornell, Robert A.; Houston, Douglas W.; Murray, Jeffrey C.; Manak, J. Robert
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All things considered, my risk for diabetes is medium: A risk personalization process of familial risk for type 2 diabetes
err2019-10-23
err6
errOAAI
errDaack-Hirsch, Sandra; Shah, Lisa L.; Jones, Kaitlyn; Rocha, Brenda; Doerr, Megan; Gabitzsch, Emily; Meese, Thad
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Women's knowledge and use of prenatal screening tests
err2017-03-20
err29
errOAAI
errSeven, Memnun; Akyuz, Aygul; Eroglu, Kafiye; Daack-Hirsch, Sandra; Skirton, Heather
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Educating future nursing scientists: Recommendations for integrating omics content in PhD programs
err2015-07-01
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errConley, Yvette P.; Heitkemper, Margaret; McCarthy, Donna; Anderson, Cindy M.; Corwin, Elizabeth J.; Daack-Hirsch, Sandra; Dorsey, Susan G.; Gregory, Katherine E.; Groer, Maureen W.; Henly, Susan J.; Landers, Timothy; Lyon, Debra E.; Taylor, Jacquelyn Y.; Voss, Joachim
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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
err2009-04-01
err111
errOAAI
errFerreira de Lima, Renata. L. L.; Hoper, Sarah A.; Ghassibe, Michella; Cooper, Margaret E.; Rorick, Nicholas K.; Kondo, Shinji; Katz, Lori; Marazita, Mary L.; Compton, John; Bale, Sherri; Hehr, Ute; Dixon, Michael J.; Daack-Hirsch, Sandra; Boute, Odile; Bayet, Benedicte; Revencu, Nicole; Verellen-Dumoulin, Christine; Vikkula, Miikka; Richieri-Costa, Antonio; Moretti-Ferreira, Danilo; Murray, Jeffrey C.; Schutte, Brain C.
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Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip
err2009-03-01
err180
errOAAI
errSuzuki, Satoshi; Marazita, Mary L.; Cooper, Margaret E.; Miwa, Nobutomo; Hing, Anne; Jugessur, Astanand; Natsume, Nagato; Shimozato, Kazuo; Ohbayashi, Naofumi; Suzuki, Yasushi; Niimi, Teruyuki; Minami, Katsuhiro; Yamamoto, Masahiko; Altannamar, Tserendorj J.; Erkhembaatar, Tudevdorj; Furukawa, Hiroo; Daack-Hirsch, Sandra; L'Heureux, Jamie; Brandon, Carla A.; Weinberg, Seth M.; Neiswanger, Katherine; Deleyiannis, Frederic W. B.; de Salamanca, Javier E.; Vieira, Alexandre R.; Lidral, Andrew C.; Martin, James F.; Murray, Jeffrey C.
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Impaired FGF signaling contributes to cleft lip and palate
err2007-03-13
err274
errOAAI
errRiley, Bridget M.; Mansilla, M. Adela; Ma, Jinghong; Daack-Hirsch, Sandra; Maher, Brion S.; Raffensperger, Lisa M.; Russo, Erilynn T.; Vieira, Alexandre R.; Dode, Catherine; Mohammadi, Moosa; Marazita, Mary L.; Murray, Jeffrey C.
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Medical sequencing of candidate genes for nonsyndromic cleft lip and palate
err2005-12-02
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errVieira, AR; Avila, JR; Daack-Hirsch, S; Dragan, E; Fèlix, TM; Rahimov, F; Harrington, J; Schultz, RR; Watanabe, Y; Johnson, M; Fang, J; O'Brien, SE; Orioli, IM; Castilla, EE; FitzPatrick, DR; Jiang, RL; Marazita, ML; Murray, JC
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Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
err2004-08-19
err544
errOAAI
errZucchero, TM; Cooper, ME; Maher, BS; Daack-Hirsch, S; Nepomuceno, B; Ribeiro, L; Caprau, D; Christensen, K; Suzuki, Y; Machida, J; Natsume, N; Yoshiura, KI; Vieira, AR; Orioli, IM; Castilla, EE; Moreno, L; Arcos-Burgos, M; Lidral, AC; Field, LL; Liu, YE; Ray, A; Goldstein, TH; Schultz, RE; Shi, M; Johnson, MK; Kondo, S; Schutte, BC; Marazita, ML; Murray, JC
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Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
err2004-08-01
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errMarazita, ML; Murray, JC; Lidral, AC; Arcos-Burgos, M; Cooper, ME; Goldstein, T; Maher, BS; Daack-Hirsch, S; Schultz, R; Mansilla, MA; Field, LL; Liu, Y; Prescott, N; Malcolm, S; Winter, R; Ray, A; Moreno, L; Valencia, C; Neiswanger, K; Wyszynski, DF; Bailey-Wilson, JE; Albacha-Hejazi, H; Beaty, TH; McIntosh, I; Hetmanski, JB; Tunçbilek, G; Edwards, M; Harkin, L; Scott, R; Roddick, LG
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Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
err2002-09-03
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errKondo, S; Schutte, BC; Richardson, RJ; Bjork, BC; Knight, AS; Watanabe, Y; Howard, E; de Lima, RLLF; Daack-Hirsch, S; Sander, A; McDonald-McGinn, DM; Zackai, EH; Lammer, EJ; Aylsworth, AS; Ardinger, HH; Lidral, AC; Pober, BR; Moreno, L; Arcos-Burgos, M; Valencia, C; Houdayer, C; Bahuau, M; Moretti-Ferreira, D; Richieri-Costa, A; Dixon, MJ; Murray, JC
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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
err1998-12-01
err63
PREAI
errYoshiura, K; Machida, J; Daack-Hirsch, S; Patil, SR; Ashworth, LK; Hecht, JT; Murray, JC
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Association of MSX1 and TGFB3 with nonsyndromic clefting in humans
err1998-08-01
err292
errOAAI
errLidral, AC; Romitti, PA; Basart, AM; Doetschman, T; Leysens, NJ; Daack-Hirsch, S; Semina, EV; Johnson, LR; Machida, J; Burds, A; Parnell, TJ; Rubenstein, JLR; Murray, JC
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A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
err1998-06-01
err350
PREAI
errSemina, EV; Ferrell, RE; Mintz-Hittner, HA; Bitoun, P; Alward, WLM; Reiter, RS; Funkhauser, C; Daack-Hirsch, S; Murray, JC
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The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations
err1998-01-01
err21
PREAI
errRomitti, PA; Munger, RG; Murray, JC; Daack-Hirsch, S; Hanson, JW; Burns, TL
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