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Items: 32

1.

Developmental delay, coarse facial features, and epilepsy in a patient with EXT2 gene variants.

Gupta A, Ewing SA, Renaud DL, Hasadsri L, Raymond KM, Klee EW, Gavrilova RH.

Clin Case Rep. 2019 Feb 19;7(4):632-637. doi: 10.1002/ccr3.2010. eCollection 2019 Apr.

2.

Opioid and non-opioid utilization at home following gastrointestinal procedures: a prospective cohort study.

Bartels K, Mahoney K, Raymond KM, McWilliams SK, Fernandez-Bustamante A, Schulick R, Hopfer CJ, Mikulich-Gilbertson SK.

Surg Endosc. 2019 Apr 3. doi: 10.1007/s00464-019-06767-1. [Epub ahead of print]

PMID:
30945059
3.

Testing helping behavior and its relationship to antisocial personality and psychopathic traits.

Sakai JT, Raymond KM, McWilliams SK, Mikulich-Gilbertson SK.

Psychiatry Res. 2019 Apr;274:98-104. doi: 10.1016/j.psychres.2019.02.022. Epub 2019 Feb 11.

PMID:
30780067
4.

The Association of Patient Satisfaction-Based Incentives with Primary Care Physician Opioid Prescribing.

Carrico JA, Mahoney K, Raymond KM, Mims L, Smith PC, Sakai JT, Mikulich-Gilbertson SK, Hopfer CJ, Bartels K.

J Am Board Fam Med. 2018 Nov-Dec;31(6):941-943. doi: 10.3122/jabfm.2018.06.180067.

5.

A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.

Ferreira CR, Xia ZJ, Clément A, Parry DA, Davids M, Taylan F, Sharma P, Turgeon CT, Blanco-Sánchez B, Ng BG, Logan CV, Wolfe LA, Solomon BD, Cho MT, Douglas G, Carvalho DR, Bratke H, Haug MG, Phillips JB, Wegner J, Tiemeyer M, Aoki K; Undiagnosed Diseases Network; Scottish Genome Partnership, Nordgren A, Hammarsjö A, Duker AL, Rohena L, Hove HB, Ek J, Adams D, Tifft CJ, Onyekweli T, Weixel T, Macnamara E, Radtke K, Powis Z, Earl D, Gabriel M, Russi AHS, Brick L, Kozenko M, Tham E, Raymond KM, Phillips JA 3rd, Tiller GE, Wilson WG, Hamid R, Malicdan MCV, Nishimura G, Grigelioniene G, Jackson A, Westerfield M, Bober MB, Gahl WA, Freeze HH.

Am J Hum Genet. 2018 Oct 4;103(4):553-567. doi: 10.1016/j.ajhg.2018.09.003.

6.

Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency.

Hall PL, Lam C, Alexander JJ, Asif G, Berry GT, Ferreira C, Freeze HH, Gahl WA, Nickander KK, Sharer JD, Watson CM, Wolfe L, Raymond KM.

Mol Genet Metab. 2018 May;124(1):82-86. doi: 10.1016/j.ymgme.2018.03.002. Epub 2018 Mar 10.

PMID:
29550355
7.

Probable Diagnosis of a Patient with Niemann-Pick Disease Type C: Managing Pitfalls of Exome Sequencing.

Zeiger WA, Jamal NI, Scheuner MT, Pittman P, Raymond KM, Morra M, Mishra SK.

JIMD Rep. 2018;41:47-51. doi: 10.1007/8904_2018_90. Epub 2018 Feb 17.

8.

Cannabis use disorder and male sex predict medical cannabis card status in a sample of high risk adolescents.

Kim J, Coors ME, Young SE, Raymond KM, Hopfer CJ, Wall TL, Corley RP, Brown SA, Sakai JT.

Drug Alcohol Depend. 2018 Feb 1;183:25-33. doi: 10.1016/j.drugalcdep.2017.11.007. Epub 2017 Dec 2.

9.

Children's brain activation during risky decision-making: A contributor to substance problems?

Crowley TJ, Dalwani MS, Sakai JT, Raymond KM, McWilliams SK, Banich MT, Mikulich-Gilbertson SK.

Drug Alcohol Depend. 2017 Sep 1;178:57-65. doi: 10.1016/j.drugalcdep.2017.02.028. Epub 2017 Jun 4.

10.

Simultaneous Testing for 6 Lysosomal Storage Disorders and X-Adrenoleukodystrophy in Dried Blood Spots by Tandem Mass Spectrometry.

Tortorelli S, Turgeon CT, Gavrilov DK, Oglesbee D, Raymond KM, Rinaldo P, Matern D.

Clin Chem. 2016 Sep;62(9):1248-54. doi: 10.1373/clinchem.2016.256255. Epub 2016 Jul 20.

11.

A Behavioral Measure of Costly Helping: Replicating and Extending the Association with Callous Unemotional Traits in Male Adolescents.

Sakai JT, Dalwani MS, Mikulich-Gilbertson SK, McWilliams SK, Raymond KM, Crowley TJ.

PLoS One. 2016 Mar 15;11(3):e0151678. doi: 10.1371/journal.pone.0151678. eCollection 2016.

12.

Adolescents with substance use disorder and assent/consent: Empirical data on understanding biobank risks in genomic research.

Coors ME, Raymond KM, Hopfer CJ, Sakai J, McWilliams SK, Young S, Mikulich-Gilbertson SK.

Drug Alcohol Depend. 2016 Feb 1;159:267-71. doi: 10.1016/j.drugalcdep.2015.12.006. Epub 2015 Dec 21.

13.

Adolescents' Neural Processing of Risky Decisions: Effects of Sex and Behavioral Disinhibition.

Crowley TJ, Dalwani MS, Mikulich-Gilbertson SK, Young SE, Sakai JT, Raymond KM, McWilliams SK, Roark MJ, Banich MT.

PLoS One. 2015 Jul 15;10(7):e0132322. doi: 10.1371/journal.pone.0132322. eCollection 2015.

14.

Female adolescents with severe substance and conduct problems have substantially less brain gray matter volume.

Dalwani MS, McMahon MA, Mikulich-Gilbertson SK, Young SE, Regner MF, Raymond KM, McWilliams SK, Banich MT, Tanabe JL, Crowley TJ, Sakai JT.

PLoS One. 2015 May 22;10(5):e0126368. doi: 10.1371/journal.pone.0126368. eCollection 2015.

15.

Adolescent perspectives on the return of individual results in genomic addiction research.

Coors ME, Raymond KM, McWilliams SK, Hopfer CJ, Mikulich-Gilbertson SK.

Psychiatr Genet. 2015 Jun;25(3):127-30. doi: 10.1097/YPG.0000000000000083.

16.

What adolescents enrolled in genomic addiction research want to know about conflicts of interest.

Coors ME, Raymond KM, McWilliams SK, Hopfer CJ, Mikulich-Gilbertson SK.

Drug Alcohol Depend. 2015 Feb 1;147:272-5. doi: 10.1016/j.drugalcdep.2014.12.004. Epub 2014 Dec 15.

17.

PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.

Stray-Pedersen A, Backe PH, Sorte HS, Mørkrid L, Chokshi NY, Erichsen HC, Gambin T, Elgstøen KB, Bjørås M, Wlodarski MW, Krüger M, Jhangiani SN, Muzny DM, Patel A, Raymond KM, Sasa GS, Krance RA, Martinez CA, Abraham SM, Speckmann C, Ehl S, Hall P, Forbes LR, Merckoll E, Westvik J, Nishimura G, Rustad CF, Abrahamsen TG, Rønnestad A, Osnes LT, Egeland T, Rødningen OK, Beck CR; Baylor-Johns Hopkins Center for Mendelian Genomics, Boerwinkle EA, Gibbs RA, Lupski JR, Orange JS, Lausch E, Hanson IC.

Am J Hum Genet. 2014 Jul 3;95(1):96-107. doi: 10.1016/j.ajhg.2014.05.007. Epub 2014 Jun 12.

18.

Discordant results between biochemical and molecular transthyretin assays: lessons learned from a unique testing algorithm at the Mayo Clinic.

Reddi HV, Thomas BC, Willkomm KS, Ferber MJ, Rumilla KM, Raymond KM, O'Brien JF, Highsmith WE.

J Genet. 2013 Dec;92(3):599-604. No abstract available.

19.

Default mode network activity in male adolescents with conduct and substance use disorder.

Dalwani MS, Tregellas JR, Andrews-Hanna JR, Mikulich-Gilbertson SK, Raymond KM, Banich MT, Crowley TJ, Sakai JT.

Drug Alcohol Depend. 2014 Jan 1;134:242-250. doi: 10.1016/j.drugalcdep.2013.10.009. Epub 2013 Oct 24.

20.

Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy.

Yang AC, Ng BG, Moore SA, Rush J, Waechter CJ, Raymond KM, Willer T, Campbell KP, Freeze HH, Mehta L.

Mol Genet Metab. 2013 Nov;110(3):345-351. doi: 10.1016/j.ymgme.2013.06.016. Epub 2013 Jun 28.

21.

Pregnancy in an individual with mild Smith-Lemli-Opitz syndrome.

Ellingson MS, Wick MJ, White WM, Raymond KM, Saenger AK, Pichurin PN, Wassif CA, Porter FD, Babovic-Vuksanovic D.

Clin Genet. 2014 May;85(5):495-7. doi: 10.1111/cge.12209. Epub 2013 Jun 24. No abstract available.

22.

Risky decisions and their consequences: neural processing by boys with Antisocial Substance Disorder.

Crowley TJ, Dalwani MS, Mikulich-Gilbertson SK, Du YP, Lejuez CW, Raymond KM, Banich MT.

PLoS One. 2010 Sep 22;5(9):e12835. doi: 10.1371/journal.pone.0012835.

23.

Determination of total homocysteine, methylmalonic acid, and 2-methylcitric acid in dried blood spots by tandem mass spectrometry.

Turgeon CT, Magera MJ, Cuthbert CD, Loken PR, Gavrilov DK, Tortorelli S, Raymond KM, Oglesbee D, Rinaldo P, Matern D.

Clin Chem. 2010 Nov;56(11):1686-95. doi: 10.1373/clinchem.2010.148957. Epub 2010 Aug 31.

24.

Safety status of farm tractors that operate on public highways in four rural Kentucky counties.

Cole HP, Piercy LR, Heinz KL, Westneat SC, Arrowsmith HE, Raymond KM.

J Agric Saf Health. 2009 Jul;15(3):207-23.

PMID:
19728545
25.

Substance use disorder genetic research: investigators and participants grapple with the ethical issues.

Coors ME, Raymond KM.

Psychiatr Genet. 2009 Apr;19(2):83-90. doi: 10.1097/YPG.0b013e328320800e.

26.

Brain activation during the Stroop task in adolescents with severe substance and conduct problems: A pilot study.

Banich MT, Crowley TJ, Thompson LL, Jacobson BL, Liu X, Raymond KM, Claus ED.

Drug Alcohol Depend. 2007 Oct 8;90(2-3):175-82. Epub 2007 May 11.

27.

Host, macrohabitat, and microhabitat specificity in the gill parasite Afrodiplozoon polycotyleus (Monogenea).

Raymond KM, Chapman LL, Lanciani CA.

J Parasitol. 2006 Dec;92(6):1211-7.

PMID:
17304797
28.

Measuring impulsivity in adolescents with serious substance and conduct problems.

Thompson LL, Whitmore EA, Raymond KM, Crowley TJ.

Assessment. 2006 Mar;13(1):3-15.

PMID:
16443715
29.

A risk-taking "set" in a novel task among adolescents with serious conduct and substance problems.

Crowley TJ, Raymond KM, Mikulich-Gilbertson SK, Thompson LL, Lejuez CW.

J Am Acad Child Adolesc Psychiatry. 2006 Feb;45(2):175-83.

PMID:
16429088
30.

Binding of ferric enterobactin by the Escherichia coli periplasmic protein FepB.

Sprencel C, Cao Z, Qi Z, Scott DC, Montague MA, Ivanoff N, Xu J, Raymond KM, Newton SM, Klebba PE.

J Bacteriol. 2000 Oct;182(19):5359-64.

31.

[Prevalence study of biotinidase deficiency in newborns].

Pinto AL, Raymond KM, Bruck I, Antoniuk SA.

Rev Saude Publica. 1998 Apr;32(2):148-52. Portuguese.

PMID:
9713119
32.

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