SCOTTMCLEANSCOTT MCLEAN0.000000000000000.000000000000007004MCLEAN, SCOTTProfessorprns:coAuthorOfcoauthor ofFaculty Rankprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:mediaLinksmedia linksprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:physicalNeighborOfphysical neighborprns:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:similarTosimilar toprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAddressvivo:address1address line 1vivo:addressCitycityvivo:addressPostalCodepostal codevivo:authorInAuthorshipselected publicationsvivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionvivo:hasResearchArearesearch areasvivo:hrJobTitleHR job titleInformation Resourcevivo:linkAnchorTextlink anchor textvivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcevivo:mailingAddressmailing addressvivo:orcidIdORCID idvivo:personInPositionpositionsPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titleURLLinkvivo:webpagewebpagerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson74Professor10Assistant Professor14Associate Professor42Director47Distinguished Service ProfessorAuthorship 3268011327545676Tokita MJ, Braxton AA, Shao Y, Lewis AM, Vincent M, K?ry S, Besnard T, Isidor B, Latypova X, B?zieau S, Liu P, Motter CS, Melver CW, Robin NH, Infante EM, McGuire M, El-Gharbawy A, Littlejohn RO, McLean SD, Bi W, Bacino CA, Lalani SR, Scott DA, Eng CM, Yang Y, Schaaf CP, Walkiewicz MAAmerican journal of human geneticsDe Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive. Am J Hum Genet. 2016 09 01; 99(3):720-727.Am J Hum Genet2016-08-18T00:00:002016De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive.19346217Lacbawan F, Solomon BD, Roessler E, El-Jaick K, Domen? S, V?lez JI, Zhou N, Hadley D, Balog JZ, Long R, Fryer A, Smith W, Omar S, McLean SD, Clarkson K, Lichty A, Clegg NJ, Delgado MR, Levey E, Stashinko E, Potocki L, Vanallen MI, Clayton-Smith J, Donnai D, Bianchi DW, Juliusson PB, Nj?lstad PR, Brunner HG, Carey JC, Hehr U, M?sebeck J, Wieacker PF, Postra A, Hennekam RC, van den Boogaard MJ, van Haeringen A, Paulussen A, Herbergs J, Schrander-Stumpel CT, Janecke AR, Chitayat D, Hahn J, McDonald-McGinn DM, Zackai EH, Dobyns WB, Muenke MJournal of medical geneticsClinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. J Med Genet. 2009 Jun; 46(6):389-98.J Med Genet2009-04-02T00:00:002009Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.21925314Liu P, Erez A, Nagamani SC, Dhar SU, Kolodziejska KE, Dharmadhikari AV, Cooper ML, Wiszniewska J, Zhang F, Withers MA, Bacino CA, Campos-Acevedo LD, Delgado MR, Freedenberg D, Garnica A, Grebe TA, Hern?ndez-Almaguer D, Immken L, Lalani SR, McLean SD, Northrup H, Scaglia F, Strathearn L, Trapane P, Kang SH, Patel A, Cheung SW, Hastings PJ, Stankiewicz P, Lupski JR, Bi WCellChromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. Cell. 2011 Sep 16; 146(6):889-903.Cell2011-09-16T00:00:002011Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.JEREMYSCHRAWJEREMY SCHRAW12525SCHRAW, JEREMY0000-0002-6674-9562Assistant ProfessorAuthorship 8402483Authorship 840249619795528Lin AE, Yuzuriha S, McLean S, Mulliken JBThe Journal of craniofacial surgeryLesser forms of cleft lip associated with the branchio-oculo-facial syndrome. J Craniofac Surg. 2009 Mar; 20 Suppl 1:608-11.J Craniofac Surg2009-03-01T00:00:002009Lesser forms of cleft lip associated with the branchio-oculo-facial syndrome.8545206Hagerman RJ, Staley LW, O'Conner R, Lugenbeel K, Nelson D, McLean SD, Taylor APediatricsLearning-disabled males with a fragile X CGG expansion in the upper premutation size range. Pediatrics. 1996 Jan; 97(1):122-6.Pediatrics1996-01-01T00:00:001996Learning-disabled males with a fragile X CGG expansion in the upper premutation size range.Authorship 8703232428575647Gabriele M, Vulto-van Silfhout AT, Germain PL, Vitriolo A, Kumar R, Douglas E, Haan E, Kosaki K, Takenouchi T, Rauch A, Steindl K, Frengen E, Misceo D, Pedurupillay CRJ, Stromme P, Rosenfeld JA, Shao Y, Craigen WJ, Schaaf CP, Rodriguez-Buritica D, Farach L, Friedman J, Thulin P, McLean SD, Nugent KM, Morton J, Nicholl J, Andrieux J, Stray-Pedersen A, Chambon P, Patrier S, Lynch SA, Kjaergaard S, T?rring PM, Brasch-Andersen C, Ronan A, van Haeringen A, Anderson PJ, Powis Z, Brunner HG, Pfundt R, Schuurs-Hoeijmakers JHM, van Bon BWM, Lelieveld S, Gilissen C, Nillesen WM, Vissers LELM, Gecz J, Koolen DA, Testa G, de Vries BBAAmerican journal of human geneticsYY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. Am J Hum Genet. 2017 Jun 01; 100(6):907-925.Am J Hum Genet2017-06-01T00:00:002017YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.Authorship 8735452028667181von Spiczak S, Helbig KL, Shinde DN, Huether R, Pendziwiat M, Louren?o C, Nunes ME, Sarco DP, Kaplan RA, Dlugos DJ, Kirsch H, Slavotinek A, Cilio MR, Cervenka MC, Cohen JS, McClellan R, Fatemi A, Yuen A, Sagawa Y, Littlejohn R, McLean SD, Hernandez-Hernandez L, Maher B, M?ller RS, Palmer E, Lawson JA, Campbell CA, Joshi CN, Kolbe DL, Hollingsworth G, Neubauer BA, Muhle H, Stephani U, Scheffer IE, Pena SDJ, Sisodiya SM, Helbig I, Epi4K Consortium, EuroEPINOMICS-RES NLES Working GroupNeurologyDNM1 encephalopathy: A new disease of vesicle fission. Neurology. 2017 Jul 25; 89(4):385-394.Neurology2017-06-30T00:00:002017DNM1 encephalopathy: A new disease of vesicle fission.Authorship 877241228807008Bostwick BL, McLean S, Posey JE, Streff HE, Gripp KW, Blesson A, Powell-Hamilton N, Tusi J, Stevenson DA, Farrelly E, Hudgins L, Yang Y, Xia F, Wang X, Liu P, Walkiewicz M, McGuire M, Grange DK, Andrews MV, Hummel M, Madan-Khetarpal S, Infante E, Coban-Akdemir Z, Miszalski-Jamka K, Jefferies JL, Members of the Undiagnosed Diseases Network, Rosenfeld JA, Emrick L, Nugent KM, Lupski JR, Belmont JW, Lee B, Lalani SRGenome medicinePhenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders. Genome Med. 2017 08 14; 9(1):73.Genome Med2017-08-14T00:00:002017Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders.Authorship 8777242Authorship 87772512159613Barker JA, McLean SD, Jordan GD, Krober MS, Rawlings JSThe Pediatric infectious disease journalPrimary neonatal herpes simplex virus pneumonia. Pediatr Infect Dis J. 1990 Apr; 9(4):285-9.Pediatr Infect Dis J1990-04-01T00:00:001990Primary neonatal herpes simplex virus pneumonia.1287646McLean S, Stanley W, Stern H, Fonda-Allen J, Devine G, Ellingham T, Rosenbaum KPrenatal diagnosisPrenatal diagnosis of Pallister-Killian syndrome: resolution of cytogenetic ambiguity by use of fluorescent in situ hybridization. Prenat Diagn. 1992 Dec; 12(12):985-91.Prenat Diagn1992-12-01T00:00:001992Prenatal diagnosis of Pallister-Killian syndrome: resolution of cytogenetic ambiguity by use of fluorescent in situ hybridization.true1Associate ProfessorAssociate Professortrue1ProfessorProfessortrue1ProfessorProfessorD008607Disorders24810220.567045Intellectual Disability29861108Reijnders MRF, Miller KA, Alvi M, Goos JAC, Lees MM, de Burca A, Henderson A, Kraus A, Mikat B, de Vries BBA, Isidor B, Kerr B, Marcelis C, Schluth-Bolard C, Deshpande C, Ruivenkamp CAL, Wieczorek D, Deciphering Developmental Disorders Study, Baralle D, Blair EM, Engels H, L?decke HJ, Eason J, Santen GWE, Clayton-Smith J, Chandler K, Tatton-Brown K, Payne K, Helbig K, Radtke K, Nugent KM, Cremer K, Strom TM, Bird LM, Sinnema M, Bitner-Glindzicz M, van Dooren MF, Alders M, Koopmans M, Brick L, Kozenko M, Harline ML, Klaassens M, Steinraths M, Cooper NS, Edery P, Yap P, Terhal PA, van der Spek PJ, Lakeman P, Taylor RL, Littlejohn RO, Pfundt R, Mercimek-Andrews S, Stegmann APA, Kant SG, McLean S, Joss S, Swagemakers SMA, Douzgou S, Wall SA, K?ry S, Calpena E, Koelling N, McGowan SJ, Twigg SRF, Mathijssen IMJ, Nellaker C, Brunner HG, Wilkie AOMAmerican journal of human geneticsDe Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder. Am J Hum Genet. 2018 06 07; 102(6):1195-1203.Am J Hum Genet2018-05-31T00:00:002018De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder.D006804Occupations16300.96671ErgonomicsD012308Procedures761070.915614Risk ManagementD013177Activities & Behaviors49810.916445SportsD013597Activities & BehaviorsOccupations14170.982157Systems AnalysisCHSA Pedi-GeneticsELIZABETHROEDERELIZABETH ROEDER0.000000000000000.000000000000005526ROEDER, ELIZABETHAssociate ProfessorDepartment of PediatricsDepartment of Molecular & Human GeneticsMolecular & Human GeneticsPediatrics-Critical CarePediatrics-Emergency MedicinePediatrics-Hematology & OncologyBaylor College of MedicineDANIELLEMKEDANIEL LEMKE0.000000000000000.000000000000002223LEMKE, DANIELAssociate ProfessorJAMESLUPSKIJAMES LUPSKI29.71073630000000-95.396604500000003140LUPSKI, JAMESProfessorMALCOLMBRENNERMALCOLM BRENNER0.000000000000000.000000000000003564BRENNER, MALCOLMDistinguished Service ProfessorMICHAELWANGLERMICHAEL WANGLER29.71009470000000-95.397401400000003839WANGLER, MICHAELAssociate ProfessorMATTHEWMUSICKMATTHEW MUSICK0.000000000000000.000000000000003906MUSICK, MATTHEWAssociate ProfessorPAWELSTANKIEWICZPAWEL STANKIEWICZ29.71073630000000-95.39660450000000166STANKIEWICZ, PAWELProfessorRICHARDGIBBSRICHARD GIBBS0.000000000000000.000000000000003131GIBBS, RICHARDDistinguished Service ProfessorSEEMALALANISEEMA LALANI29.71306600000000-95.39705500000000391LALANI, SEEMAProfessorPHILIPLUPOPHILIP LUPO29.70508570000000-95.401808700000004333LUPO, PHILIP0000-0003-0978-5863ProfessorSARAHELSEASARAH ELSEA0.000000000000000.000000000000004693ELSEA, SARAHProfessorAuthorship 9521341431313535Benjamin RH, Yu X, Navarro Sanchez ML, Chen H, Mitchell LE, Langlois PH, Canfield MA, Swartz MD, Scheuerle AE, Scott DA, Northrup H, Schaaf CP, Ray JW, McLean SD, Lupo PJ, Agopian AJBirth defects researchCo-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries. Birth Defects Res. 2019 11 01; 111(18):1356-1364.Birth Defects Res2019-07-16T00:00:002019Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries.true1Distinguished Service ProfessorDistinguished Service ProfessorAuthorship 9616441931769566Assia Batzir N, Kishor Bhagwat P, Larson A, Coban Akdemir Z, Baglaj M, Bofferding L, Bosanko KB, Bouassida S, Callewaert B, Cannon A, Enchautegui Colon Y, Garnica AD, Harr MH, Heck S, Hurst ACE, Jhangiani SN, Isidor B, Littlejohn RO, Liu P, Magoulas P, Mar Fan H, Marom R, McLean S, Nezarati MM, Nugent KM, Petersen MB, Rocha ML, Roeder E, Smigiel R, Tully I, Weisfeld-Adams J, Wells KO, Baylor-Hopkins Center for Mendelian Genomics, Posey JE, Lupski JR, Beaudet AL, Wangler MFHuman mutationRecurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy. Hum Mutat. 2020 03; 41(3):641-654.Hum Mutat2019-12-19T00:00:002019Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy.Authorship 9747811131883306Sewani M, Nugent K, Blackburn PR, Tarnowski JM, Hernandez-Garcia A, Amiel J, Whalen S, Keren B, Courtin T, Rosenfeld JA, Yang Y, Patterson MC, Pichurin P, McLean SD, Scott DAAmerican journal of medical genetics. Part AFurther delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONO. Am J Med Genet A. 2020 04; 182(4):652-658.Am J Med Genet A2019-12-28T00:00:002019Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONO.Authorship 9777861232042906Johannesen KM, Mitter D, Janowski R, Roth C, Toulouse J, Poulat AL, Ville DM, Chatron N, Brilstra E, Geleijns K, Born AP, McLean S, Nugent K, Baynam G, Poulton C, Dreyer L, Gration D, Schulz S, Dieckmann A, Helbig KL, Merkenschlager A, Jamra R, Finck A, Gardella E, Hjalgrim H, Mirzaa G, Brancati F, Bierhals T, Denecke J, Hempel M, Lemke JR, Rubboli G, Muschke P, Guerrini R, Vetro A, Niessing D, Lesca G, M?ller RSNeurology. GeneticsDefining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy. Neurol Genet. 2019 Dec; 5(6):e373.Neurol Genet2019-12-10T00:00:002019Defining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy.Authorship 97887950Authorship 979122432165008Davids M, Menezes M, Guo Y, McLean SD, Hakonarson H, Collins F, Worgan L, Billington CJ, Maric I, Littlejohn RO, Onyekweli T, Adams DR, Tifft CJ, Gahl WA, Wolfe LA, Christodoulou J, Malicdan MCVMolecular genetics and metabolismHomozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency. Mol Genet Metab. 2020 05; 130(1):49-57.Mol Genet Metab2020-02-10T00:00:002020Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency.Authorship 983472316995592Pinsker JE, Rogers W, McLean S, Schaefer FV, Fenton CJournal of pediatric endocrinology & metabolism : JPEMPseudohypoparathyroidism type 1a with congenital hypothyroidism. J Pediatr Endocrinol Metab. 2006 Aug; 19(8):1049-52.J Pediatr Endocrinol Metab2006-08-01T00:00:002006Pseudohypoparathyroidism type 1a with congenital hypothyroidism.true1Associate ProfessorAssociate ProfessorAuthorship 9934151132041486Hanks JE, Kovatch KJ, Ali SA, Roberts E, Durham AB, Smith JD, Bradford CR, Malloy KM, Boonstra PS, Lao CD, McLean SAOtolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck SurgerySentinel Lymph Node Biopsy in Head and Neck Melanoma: Long-term Outcomes, Prognostic Value, Accuracy, and Safety. Otolaryngol Head Neck Surg. 2020 04; 162(4):520-529.Otolaryngol Head Neck Surg2020-02-11T00:00:002020Sentinel Lymph Node Biopsy in Head and Neck Melanoma: Long-term Outcomes, Prognostic Value, Accuracy, and Safety.true1ProfessorProfessorAuthorship 9986621332885608Oluwafemi OO, Benjamin RH, Navarro Sanchez ML, Scheuerle AE, Schaaf CP, Mitchell LE, Langlois PH, Canfield MA, Swartz MD, Scott DA, Northrup H, Ray JW, McLean SD, Ludorf KL, Chen H, Lupo PJ, Agopian AJAmerican journal of medical genetics. Part ABirth defects that co-occur with non-syndromic gastroschisis and omphalocele. Am J Med Genet A. 2020 11; 182(11):2581-2593.Am J Med Genet A2020-09-04T00:00:002020Birth defects that co-occur with non-syndromic gastroschisis and omphalocele.Authorship 9987821230548484Smith JD, Birkeland AC, Rosko AJ, Hoesli RC, Foltin SK, Swiecicki P, Mierzwa M, Chinn SB, Shuman AG, Malloy KM, Casper KA, McLean SA, Wolf GT, Bradford CR, Prince ME, Brenner JC, Spector MEHead & neckMutational profiles of persistent/recurrent laryngeal squamous cell carcinoma. Head Neck. 2019 02; 41(2):423-428.Head Neck2018-12-12T00:00:002018Mutational profiles of persistent/recurrent laryngeal squamous cell carcinoma.https://www.bcm.edu/people-search/jeremy-schraw-30314BCM Signature pagehttps://www.linkedin.com/in/jeremy-schraw-05526498/LinkedInAuthorship 1004672233161182Hulme A, McLean S, Dallat C, Walker GH, Waterson P, Stanton NA, Salmon PMApplied ergonomicsSystems thinking-based risk assessment methods applied to sports performance: A comparison of STPA, EAST-BL, and Net-HARMS in the context of elite women's road cycling. Appl Ergon. 2021 Feb; 91:103297.Appl Ergon2020-11-05T00:00:002020Systems thinking-based risk assessment methods applied to sports performance: A comparison of STPA, EAST-BL, and Net-HARMS in the context of elite women's road cycling.Authorship 1006485433281045Ludorf KL, Benjamin RH, Navarro Sanchez ML, McLean SD, Northrup H, Mitchell LE, Langlois PH, Canfield MA, Scheuerle AE, Scott DA, Schaaf CP, Ray JW, Oluwafemi O, Chen H, Swartz MD, Lupo PJ, Agopian AJJournal of pediatric urologyPatterns of co-occurring birth defects among infants with hypospadias. J Pediatr Urol. 2021 02; 17(1):64.e1-64.e8.J Pediatr Urol2020-11-12T00:00:002020Patterns of co-occurring birth defects among infants with hypospadias.Authorship 10074001Authorship 10074012Authorship 1007408633344972McLean S, Read GJM, Hulme A, Dodd K, Gorman AD, Solomon C, Salmon PMFrontiers in sports and active livingBeyond the Tip of the Iceberg: Using Systems Archetypes to Understand Common and Recurring Issues in Sports Coaching. Front Sports Act Living. 2019; 1:49.Front Sports Act Living2019-10-16T00:00:002019Beyond the Tip of the Iceberg: Using Systems Archetypes to Understand Common and Recurring Issues in Sports Coaching.33344979Hulme A, McLean S, Read GJM, Dallat C, Bedford A, Salmon PMFrontiers in sports and active livingSports Organizations as Complex Systems: Using Cognitive Work Analysis to Identify the Factors Influencing Performance in an Elite Netball Organization. Front Sports Act Living. 2019; 1:56.Front Sports Act Living2019-11-04T00:00:002019Sports Organizations as Complex Systems: Using Cognitive Work Analysis to Identify the Factors Influencing Performance in an Elite Netball Organization.33345678Schraw JM, Benjamin RH, Scott DA, Brooks BP, Hufnagel RB, McLean SD, Northrup H, Langlois PH, Canfield MA, Scheuerle AE, Schaaf CP, Ray JW, Chen H, Swartz MD, Mitchell LE, Agopian AJ, Lupo PJOphthalmic epidemiologyA Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or Microphthalmia. Ophthalmic Epidemiol. 2021 10; 28(5):428-435.Ophthalmic Epidemiol2020-12-20T00:00:002020A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or Microphthalmia.Authorship 1009905133493871McLean S, Read GJ, Ramsay K, Hogarth L, Kean BApplied ergonomicsDesigning success: Applying Cognitive Work Analysis to optimise a para sport system. Appl Ergon. 2021 May; 93:103369.Appl Ergon2021-01-22T00:00:002021Designing success: Applying Cognitive Work Analysis to optimise a para sport system.Authorship 10106831733547200Harms KL, Zhao L, Johnson B, Wang X, Carskadon S, Palanisamy N, Rhodes DR, Mannan R, Vo JN, Choi JE, Chan MP, Fullen DR, Patel RM, Siddiqui J, Ma VT, Hrycaj S, McLean SA, Hughes TM, Bichakjian CK, Tomlins SA, Harms PWClinical cancer research : an official journal of the American Association for Cancer ResearchVirus-positive Merkel Cell Carcinoma Is an Independent Prognostic Group with Distinct Predictive Biomarkers. Clin Cancer Res. 2021 05 01; 27(9):2494-2504.Clin Cancer Res2021-02-05T00:00:002021Virus-positive Merkel Cell Carcinoma Is an Independent Prognostic Group with Distinct Predictive Biomarkers.Authorship 1010870133551908McLean S, Rath D, Lethlean S, Hornsby M, Gallagher J, Anderson D, Salmon PMFrontiers in psychologyWith Crisis Comes Opportunity: Redesigning Performance Departments of Elite Sports Clubs for Life After a Global Pandemic. Front Psychol. 2020; 11:588959.Front Psychol2021-01-20T00:00:002021With Crisis Comes Opportunity: Redesigning Performance Departments of Elite Sports Clubs for Life After a Global Pandemic.Authorship 10143421333749998Diaz D, Benjamin RH, Navarro Sanchez ML, Mitchell LE, Langlois PH, Canfield MA, Chen H, Scheuerle AE, Schaaf CP, Scott DA, Northrup H, Ray JW, McLean SD, Swartz MD, Ludorf KL, Lupo PJ, Agopian AJAmerican journal of medical genetics. Part APatterns of congenital anomalies among individuals with trisomy 13 in Texas. Am J Med Genet A. 2021 06; 185(6):1787-1793.Am J Med Genet A2021-03-22T00:00:002021Patterns of congenital anomalies among individuals with trisomy 13 in Texas.Authorship 10171351233906455Sanchez MLN, Benjamin RH, Mitchell LE, Langlois PH, Canfield MA, Swartz MD, Scheuerle AE, Scott DA, Northrup H, Schaaf CP, Ray JW, McLean SD, Chen H, Lupo PJ, Agopian AJThe Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial AssociationBirth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate. Cleft Palate Craniofac J. 2022 Apr; 59(4):417-426.Cleft Palate Craniofac J2021-04-28T00:00:002021Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate.true1Assistant ProfessorAssistant Professor6/24/2019https://www.healio.com/news/hematology-oncology/20190624/birth-defects-linked-to-increased-risk-for-Birth defects linked to increased risk for childhood cancer6/20/2019https://medicalxpress.com/news/2019-06-birth-defects-affect-childhood-cancer.htmlHow do birth defects affect childhood cancer risk?8/24/2019https://www.bcm.edu/news/factors-linked-poor-treatment-outcomes-allFactors linked to poor treatment outcomes in ALL5/29/2020https://www.bcm.edu/news/assessing-cancer-diagnosis-in-children-with-birth-defectsAssessing cancer diagnosis in children with birth defects6/20/2019https://www.bcm.edu/news/study-reveals-cancer-risk-birth-defectsStudy reveals elevated cancer risk in children with birth defects4/29/2020https://cac2.org/cancer-in-children-with-birth-defects-what-can-we-learn-from-population-based-studiCancer in Children with Birth Defects: What Can We Learn from Population-Based Studies Authorship 10208224434113002Tremblay-Lagani?re C, Maroofian R, Nguyen TTM, Karimiani EG, Kirmani S, Akbar F, Ibrahim S, Afroze B, Doosti M, Ashrafzadeh F, Babaei M, Efthymiou S, Christoforou M, Sultan T, Ladda RL, McLaughlin HM, Truty R, Mahida S, Cohen JS, Baranano K, Ismail FY, Patel MS, Lehman A, Edmondson AC, Nagy A, Walker MA, Mercimek-Andrews S, Maki Y, Sachdev R, Macintosh R, Palmer EE, Mancini GMS, Barakat TS, Steinfeld R, R?sch CT, Stettner GM, Wagner M, Wortmann SB, Kini U, Brady AF, Stals KL, Ismayilova N, Ellard S, Bernardo D, Nugent K, McLean SD, Antonarakis SE, Houlden H, Kinoshita T, Campeau PM, Murakami YGenetics in medicine : official journal of the American College of Medical GeneticsPIGG variant pathogenicity assessment reveals characteristic features within 19 families. Genet Med. 2021 10; 23(10):1873-1881.Genet Med2021-06-10T00:00:002021PIGG variant pathogenicity assessment reveals characteristic features within 19 families.Authorship 10239081Authorship 102421710Authorship 1024571334168706McLean S, Salmon PM, Gorman AD, Dodd K, Solomon CJournal of human kineticsThe Communication and Passing Contributions of Playing Positions in a Professional Soccer Team. J Hum Kinet. 2021 Jan; 77:223-234.J Hum Kinet2021-01-30T00:00:002021The Communication and Passing Contributions of Playing Positions in a Professional Soccer Team.34193968Benjamin RH, Scheuerle AE, Scott DA, Navarro Sanchez ML, Langlois PH, Canfield MA, Northrup H, Schaaf CP, Ray JW, McLean SD, Chen H, Swartz MD, Lupo PJ, Agopian AJPediatric researchBirth defect co-occurrence patterns in the Texas Birth Defects Registry. Pediatr Res. 2022 04; 91(5):1278-1285.Pediatr Res2021-06-30T00:00:002021Birth defect co-occurrence patterns in the Texas Birth Defects Registry.34230798Salmon PM, Stevens N, McLean S, Hulme A, Read GJMHuman factors and ergonomics in manufacturingHuman Factors and Ergonomics and the management of existential threats: A work domain analysis of a COVID-19 return from lockdown restrictions system. Hum Factors Ergon Manuf. 2021 Jul; 31(4):412-424.Hum Factors Ergon Manuf2021-04-06T00:00:002021Human Factors and Ergonomics and the management of existential threats: A work domain analysis of a COVID-19 return from lockdown restrictions system.Authorship 1025085834261519Ortega V, Louie RJ, Jones MA, Chaubey A, DuPont BR, Britt A, Ray J, McLean SD, Littlejohn RO, Velagaleti GMolecular cytogeneticsCopy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader-Willi/Angelman syndromes? Mol Cytogenet. 2021 Jul 14; 14(1):37.Mol Cytogenet2021-07-14T00:00:002021Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader-Willi/Angelman syndromes?Authorship 1026456434325994Ludorf KL, Benjamin RH, Navarro Sanchez ML, McLean SD, Northrup H, Mitchell LE, Langlois PH, Canfield MA, Scheuerle AE, Scott DA, Schaaf CP, Ray JW, Oluwafemi O, Chen H, Swartz MD, Lupo PJ, Agopian AJJournal of pediatric urologyCorrigendum to "Patterns of co-occurring birth defects among infants with hypospadias? [J Pediatr Urol 17 (2021) 64.e1-64.e8]. J Pediatr Urol. 2021 Aug; 17(4):e1.J Pediatr Urol2021-07-26T00:00:002021Corrigendum to "Patterns of co-occurring birth defects among infants with hypospadias? [J Pediatr Urol 17 (2021) 64.e1-64.e8].true1Distinguished Service ProfessorDistinguished Service ProfessorAuthorship 1034550134837751McLean S, Coventon L, Finch CF, Dallat C, Carden T, Salmon PMApplied ergonomicsEvaluation of a systems ergonomics-based incident reporting system. Appl Ergon. 2022 Apr; 100:103651.Appl Ergon2021-11-24T00:00:002021Evaluation of a systems ergonomics-based incident reporting system.333 NORTH SANTA ROSA ST.San Antonio, 782071.75070.0040025231research areas0.7770780.0088272640coauthor of34.55595.056360similar to1150selected publicationsREBECCALITTLEJOHNREBECCA LITTLEJOHN0.000000000000000.000000000000007008LITTLEJOHN, REBECCAAssistant Professortrue1Associate ProfessorAssociate ProfessorAuthorship 1039738135147484McLean S, Coventon L, Finch CF, Salmon PMErgonomicsIncident reporting in the outdoors: a systems-based analysis of injury, illness, and psychosocial incidents in led outdoor activities in Australia. Ergonomics. 2022 Oct; 65(10):1421-1433.Ergonomics2022-02-18T00:00:002022Incident reporting in the outdoors: a systems-based analysis of injury, illness, and psychosocial incidents in led outdoor activities in Australia.Authorship 13314512Authorship 1338511Authorship 1343431920160573McLean SDGenetics in medicine : official journal of the American College of Medical GeneticsBut is the platter really silver? Genet Med. 2010 Feb; 12(2):126.Genet Med2010-02-01T00:00:002010But is the platter really silver?12/10/2021https://blogs.bcm.edu/2021/12/10/location-location-location-does-it-impact-birth-defects/ Location. Location. Location. Does it impact birth defects?Authorship 1051052535866642McCormack P, Read GJM, Hulme A, Lane BR, McLean S, Salmon PMErgonomicsUsing systems thinking-based risk assessment methods to assess hazardous manual tasks: a comparison of Net-HARMS, EAST-BL, FRAM and STPA. Ergonomics. 2023 May; 66(5):609-626.Ergonomics2022-08-08T00:00:002022Using systems thinking-based risk assessment methods to assess hazardous manual tasks: a comparison of Net-HARMS, EAST-BL, FRAM and STPA.true1ProfessorProfessortrue1Assistant ProfessorAssistant ProfessorPediatric-Oncology EPItrue1ProfessorProfessortrue1Associate ProfessorAssociate ProfessorAuthorship 105503229Authorship 10596826Authorship 10614665736633570Roof E, Deal CL, McCandless SE, Cowan RL, Miller JL, Hamilton JK, Roeder ER, McCormack SE, Roshan Lal TR, Abdul-Latif HD, Haqq AM, Obrynba KS, Torchen LC, Vidmar AP, Viskochil DH, Chanoine JP, Lam CKL, Pierce MJ, Williams LL, Bird LM, Butler MG, Jensen DE, Myers SE, Oatman OJ, Baskaran C, Chalmers LJ, Fu C, Alos N, McLean SD, Shah A, Whitman BY, Blumenstein BA, Leonard SF, Ernest JP, Cormier JW, Cotter SP, Ryman DCThe Journal of clinical endocrinology and metabolismIntranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial. J Clin Endocrinol Metab. 2023 06 16; 108(7):1696-1708.J Clin Endocrinol Metab2023-06-16T00:00:002023Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial.36541232Schraw JM, Benjamin RH, Shumate CJ, Canfield MA, Scott DA, McLean SD, Northrup H, Scheuerle AE, Schaaf CP, Ray JW, Chen H, Agopian AJ, Lupo PJAmerican journal of medical genetics. Part APatterns of co-occurring birth defects in children with anotia and microtia. Am J Med Genet A. 2023 03; 191(3):805-812.Am J Med Genet A2022-12-21T00:00:002022Patterns of co-occurring birth defects in children with anotia and microtia.36399134Cali E, Suri M, Scala M, Ferla MP, Alavi S, Faqeih EA, Bijlsma EK, Wigby KM, Baralle D, Mehrjardi MYV, Schwab J, Platzer K, Steindl K, Hashem M, Jones M, Niyazov DM, Jacober J, Littlejohn RO, Weis D, Zadeh N, Rodan L, Goldenberg A, Lecoquierre F, Dutra-Clarke M, Horvath G, Young D, Orenstein N, Bawazeer S, Vulto-van Silfhout AT, Herenger Y, Dehghani M, Seyedhassani SM, Bahreini A, Nasab ME, Ercan-Sencicek AG, Firoozfar Z, Movahedinia M, Efthymiou S, Striano P, Karimiani EG, Salpietro V, Taylor JC, Redman M, Stegmann APA, Laner A, Abdel-Salam G, Li M, Bengala M, M?ller AJ, Digilio MC, Rauch A, Gunel M, Titheradge H, Schweitzer DN, Kraus A, Valenzuela I, McLean SD, Phornphutkul C, Salih M, Begtrup A, Schnur RE, Torti E, Haack TB, Prada CE, Alkuraya FS, Houlden H, Maroofian RGenetics in medicine : official journal of the American College of Medical GeneticsBiallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities. Genet Med. 2023 01; 25(1):135-142.Genet Med2022-11-18T00:00:002022Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities.Authorship 1063841236779796Henriquez-Lopez CJ, McLean SClinical dysmorphologyHashitoxicosis in a patient with Nicolaides-Baraitser Syndrome: a case report. Clin Dysmorphol. 2023 04 01; 32(2):77-79.Clin Dysmorphol2023-02-02T00:00:002023Hashitoxicosis in a patient with Nicolaides-Baraitser Syndrome: a case report.Authorship 1070456137028132McLean S, Naughton M, Kerherv? H, Salmon PMThe International journal on drug policyFrom Anti-doping-I to Anti-doping-II: Toward a paradigm shift for doping prevention in sport. Int J Drug Policy. 2023 05; 115:104019.Int J Drug Policy2023-04-05T00:00:002023From Anti-doping-I to Anti-doping-II: Toward a paradigm shift for doping prevention in sport.Authorship 1078585537614195Dodd K, Solomon C, Naughton M, Salmon PM, McLean STrauma, violence & abuseWhat Enables Child Sexual Abuse in Sport? A Systematic Review. Trauma Violence Abuse. 2024 04; 25(2):1599-1613.Trauma Violence Abuse2023-08-24T00:00:002023What Enables Child Sexual Abuse in Sport? A Systematic Review.Authorship 1084575821773971Erman AB, Collar RM, Griffith KA, Lowe L, Sabel MS, Bichakjian CK, Wong SL, McLean SA, Rees RS, Johnson TM, Bradford CRCancerSentinel lymph node biopsy is accurate and prognostic in head and neck melanoma. Cancer. 2012 Feb 15; 118(4):1040-7.Cancer2011-07-19T00:00:002011Sentinel lymph node biopsy is accurate and prognostic in head and neck melanoma.true1ProfessorProfessor2ProfessorProfessorAuthorship 1088262438284139Naughton M, Salmon PM, Kerherv? HA, McLean SJournal of sports sciencesApplying a systems thinking lens to anti-doping: A systematic review identifying the contributory factors to doping in sport. J Sports Sci. 2024 Jan 29; 1-15.J Sports Sci2024-01-29T00:00:002024Applying a systems thinking lens to anti-doping: A systematic review identifying the contributory factors to doping in sport.Authorship 1088385238320386Salmon PM, McLean S, Carden T, King BJ, Thompson J, Baber C, Stanton NA, Read GJMApplied ergonomicsWhen tomorrow comes: A prospective risk assessment of a future artificial general intelligence-based uncrewed combat aerial vehicle system. Appl Ergon. 2024 May; 117:104245.Appl Ergon2024-02-05T00:00:002024When tomorrow comes: A prospective risk assessment of a future artificial general intelligence-based uncrewed combat aerial vehicle system.Authorship 1090202938431799Vuocolo B, German RJ, Lalani SR, Murali CN, Bacino CA, Baskin S, Littlejohn R, Odom JD, McLean S, Schmid C, Nutter M, Stuebben M, Magness E, Juarez O, El Achi D, Mitchell B, Glinton KE, Robak L, Nagamani SC, Saba L, Ritenour A, Zhang L, Streff H, Chan K, Kemere KJ, Carter K, Texome Project, Owen N, Vossaert L, Liu P, Bellen H, Wangler MGenetics in medicine : official journal of the American College of Medical GeneticsImproving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 Feb 28; 101102.Genet Med2024-02-28T00:00:002024Improving access to exome sequencing in a medically underserved population through the Texome Project.