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Precision Population Medicine in Primary Care: The Sanford Chip Experience.
Front Genet. 2021 Mar 12;12:626845. doi: 10.3389/fgene.2021.626845. eCollection 2021.
Front Genet. 2021.
PMID: 33777099
Free PMC article.
Genesurance Counseling: Genetic Counselors' Roles and Responsibilities in Regards to Genetic Insurance and Financial Topics.
Brown S, Puumala S, Leonhard J, Bell M, Flanagan J, Dean LW, Stein Q.
Brown S, et al.
J Genet Couns. 2018 Aug;27(4):800-813. doi: 10.1007/s10897-017-0180-x. Epub 2017 Dec 4.
J Genet Couns. 2018.
PMID: 29204809
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Improved provider preparedness through an 8-part genetics and genomic education program.
Hajek C, Hutchinson AM, Galbraith LN, Green RC, Murray MF, Petry N, Preys CL, Zawatsky CLB, Zoltick ES, Christensen KD; Imagenetics METRICS Team.
Hajek C, et al.
Genet Med. 2022 Jan;24(1):214-224. doi: 10.1016/j.gim.2021.08.008. Epub 2021 Nov 30.
Genet Med. 2022.
PMID: 34906462
Free PMC article.
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Workforce Considerations When Building a Precision Medicine Program.
Blout Zawatsky CL, Leonhard JR, Bell M, Moore MM, Petry NJ, Platt DM, Green RC, Hajek C, Christensen KD.
Blout Zawatsky CL, et al. Among authors: leonhard jr.
J Pers Med. 2022 Nov 19;12(11):1929. doi: 10.3390/jpm12111929.
J Pers Med. 2022.
PMID: 36422106
Free PMC article.
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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Héron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N; Task Force for Neonatal Genomics; Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S; Deciphering Developmental Disorders Study; Hedrich UBS, Scheffer IE, Helbig I, Zampo…
See abstract for full author list ➔
Helbig KL, et al.
Am J Hum Genet. 2018 Nov 1;103(5):666-678. doi: 10.1016/j.ajhg.2018.09.006. Epub 2018 Oct 18.
Am J Hum Genet. 2018.
PMID: 30343943
Free PMC article.
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Analysis of Reimbursement of Genetic Counseling Services at a Single Institution in a State Requiring Licensure.
Leonhard JR, Munson PJ, Flanagan JD, De Berg KL, Thompson PA, Dean LW, Stein QP.
Leonhard JR, et al.
J Genet Couns. 2017 Aug;26(4):852-858. doi: 10.1007/s10897-016-0062-7. Epub 2017 Feb 8.
J Genet Couns. 2017.
PMID: 28181058
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Genetic counseling job market in the United States and Canada: An analysis of job advertisements 2014-2016.
Burns K, Swanson A, Hoskovec J, Leonhard J, Hahn S, Stein QP.
Burns K, et al.
J Genet Couns. 2019 Aug;28(4):869-877. doi: 10.1002/jgc4.1129. Epub 2019 May 6.
J Genet Couns. 2019.
PMID: 31058406
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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Héron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N; Task Force for Neonatal Genomics; Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S; Deciphering Developmental Disorders Study; Hedrich UBS, Scheffer IE, Helbig I, Zampo…
See abstract for full author list ➔
Helbig KL, et al.
Am J Hum Genet. 2019 Mar 7;104(3):562. doi: 10.1016/j.ajhg.2019.02.015.
Am J Hum Genet. 2019.
PMID: 30849329
Free PMC article.
No abstract available.
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