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Search life-sciences literature (45,103,477 articles, preprints and more)

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Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years.
Jayasinghe K, Biros E, Harris T, Wood A, O'Shea R, Hill L, Fowles L, Wardrop L, Shalhoub C, Hahn D, Rangan G, Kevin L, Tchan M, Snelling P, Sandow R, Sundaram M, Chaturvedi S, Trnka P, Faull R, [...] Mallett AJ
Kidney Int Rep, 9(8):2372-2385, 09 May 2024
Cited by: 1 article | PMID: 39156154 | PMCID: PMC11328548
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Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study.
Mallawaarachchi AC, Fowles L, Wardrop L, Wood A, O'Shea R, Biros E, Harris T, Alexander SI, Bodek S, Boudville N, Boudville N, Burke J, Burnett L, Casauria S, Chadban S, Chakera A, Crafter S, Dai P, De Fazio P, [...] Mallett AJ
Clin J Am Soc Nephrol, 19(7):887-897, 03 May 2024
Cited by: 1 article | PMID: 38861662
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Support for management actions to protect night sky quality: Insights from visitors to state and national park units in the U.S.
Beeco JA, Wilkins EJ, Miller AB, Lamborn CC, Anderson SJ, Miller ZD, Smith JW
J Environ Manage, 345:118878, 31 Aug 2023
Cited by: 0 articles | PMID: 37659363
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The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome.
Fennell AP, Baxter AE, Berkovic SF, Ellaway CJ, Forwood C, Hildebrand MS, Kumble S, McKeown C, Mowat D, Poke G, Rajagopalan S, Regan BM, Scheffer IE, Stark Z, Stutterd CA, Tan TY, Wilkins EJ, Yeung A, Hunter MF
Am J Med Genet A, 188(12):3432-3447, 17 Aug 2022
Cited by: 4 articles | PMID: 36367278
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Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.
van der Spek J, den Hoed J, Snijders Blok L, Dingemans AJM, Schijven D, Nellaker C, Venselaar H, Astuti GDN, Barakat TS, Bebin EM, Beck-Wödl S, Beunders G, Brown NJ, Brunet T, Brunner HG, Campeau PM, Čuturilo G, Gilissen C, Haack TB, [...] Kleefstra T
Genet Med, 24(6):1283-1296, 26 Mar 2022
Cited by: 8 articles | PMID: 35346573
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Inherited variants in CHD3 demonstrate variable expressivity in Snijders Blok-Campeau syndrome
van der Spek J, den Hoed J, Snijders Blok L, Dingemans AJM, Schijven D, Nellaker C, Venselaar H, Barakat TS, Bebin EM, Beck-Wödl S, Beunders G, Brown NJ, Brunet T, Brunner HG, Campeau PM, Čuturilo G, Gilissen C, Haack TB, Husain RA, [...] Kleefstra T
medRxiv, 05 Oct 2021
Cited by: 0 articles | PPR: PPR403666
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Social media reveal ecoregional variation in how weather influences visitor behavior in U.S. National Park Service units.
Wilkins EJ, Howe PD, Smith JW
Sci Rep, 11(1):2403, 28 Jan 2021
Cited by: 3 articles | PMID: 33510327 | PMCID: PMC7843642
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Uses and Limitations of Social Media to Inform Visitor Use Management in Parks and Protected Areas: A Systematic Review.
Wilkins EJ, Wood SA, Smith JW
Environ Manage, 67(1):120-132, 15 Oct 2020
Cited by: 10 articles | PMID: 33063153
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Attendance trends threaten future operations of America's state park systems.
Smith JW, Wilkins EJ, Leung YF
Proc Natl Acad Sci U S A, 116(26):12775-12780, 03 Jun 2019
Cited by: 3 articles | PMID: 31160452 | PMCID: PMC6600924
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Bringing forecasting into the future: Using Google to predict visitation in U.S. national parks.
Clark M, Wilkins EJ, Dagan DT, Powell R, Sharp RL, Hillis V
J Environ Manage, 243:88-94, 10 May 2019
Cited by: 1 article | PMID: 31082755
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Communicating information on nature-related topics: Preferred information channels and trust in sources.
Wilkins EJ, Miller HM, Tilak E, Schuster RM
PLoS One, 13(12):e0209013, 12 Dec 2018
Cited by: 3 articles | PMID: 30540834 | PMCID: PMC6291159
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Genetic Counseling in the Era of Genomics: What's all the Fuss about?
Brett GR, Wilkins EJ, Creed ET, West K, Jarmolowicz A, Valente GM, Prawer Y, Lynch E, Macciocca I
J Genet Couns, 27(5):1010-1021, 24 Jan 2018
Cited by: 4 articles | PMID: 29368275
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"It wasn't a disaster or anything": Parents' experiences of their child's uncertain chromosomal microarray result.
Wilkins EJ, Archibald AD, Sahhar MA, White SM
Am J Med Genet A, 170(11):2895-2904, 13 Jul 2016
Cited by: 20 articles | PMID: 27411073
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A DNA resequencing array for genes involved in Parkinson's disease.
Wilkins EJ, Rubio JP, Kotschet KE, Cowie TF, Boon WC, O'Hely M, Burfoot R, Wang W, Sue CM, Speed TP, Stankovitch J, Horne MK
Parkinsonism Relat Disord, 18(4):386-390, 12 Jan 2012
Cited by: 3 articles | PMID: 22243833
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Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.
Hahn CN, Chong CE, Carmichael CL, Wilkins EJ, Brautigan PJ, Li XC, Babic M, Lin M, Carmagnac A, Lee YK, Kok CH, Gagliardi L, Friend KL, Ekert PG, Butcher CM, Brown AL, Lewis ID, To LB, Timms AE, [...] Scott HS
Nat Genet, 43(10):1012-1017, 04 Sep 2011
Cited by: 364 articles | PMID: 21892162 | PMCID: PMC3184204
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RUNX1 mutations are rare in chronic phase polycythaemia vera.
Butcher CM, Neufing PJ, Eriksson L, Carmichael CL, Wilkins EJ, Melo JV, Lewis ID, Bardy PG, Scott HS, D'Andrea RJ
Br J Haematol, 153(5):672-675, 20 Feb 2011
Cited by: 1 article | PMID: 21332713
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Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips.
Ritchie ME, Liu R, Carvalho BS, Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene), Irizarry RA
BMC Bioinformatics, 12:68, 08 Mar 2011
Cited by: 28 articles | PMID: 21385424 | PMCID: PMC3063825
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Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes.
Carmichael CL, Wilkins EJ, Bengtsson H, Horwitz MS, Speed TP, Vincent PC, Young G, Hahn CN, Escher R, Scott HS
Br J Haematol, 150(3):382-385, 29 Apr 2010
Cited by: 10 articles | PMID: 20456351
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Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome.
Jongmans MC, Kuiper RP, Carmichael CL, Wilkins EJ, Dors N, Carmagnac A, Schouten-van Meeteren AY, Li X, Stankovic M, Kamping E, Bengtsson H, Schoenmakers EF, van Kessel AG, Hoogerbrugge PM, Hahn CN, Brons PP, Scott HS, Hoogerbrugge N
Leukemia, 24(1):242-246, 15 Oct 2009
Cited by: 52 articles | PMID: 19946261
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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.
Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene)
Nat Genet, 41(7):824-828, 14 Jun 2009
Cited by: 332 articles | PMID: 19525955
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Two novel JAK2 exon 12 mutations in JAK2V617F-negative polycythaemia vera patients.
Butcher CM, Hahn U, To LB, Gecz J, Wilkins EJ, Scott HS, Bardy PG, D'Andrea RJ
Leukemia, 22(4):870-873, 04 Oct 2007
Cited by: 45 articles | PMID: 17914411
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Multiplex ligation-dependent probe amplification (MLPA) genotyping assay for mouse models of down syndrome.
Hewitt CA, Carmichael CL, Wilkins EJ, Cannon PZ, Pritchard MA, Scott HS
Front Biosci, 12:3010-3016, 01 May 2007
Cited by: 6 articles | PMID: 17485278
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Authoritacanumand response to power cues.
WILKINS EJ, DECHARMS R
J Pers, 30:439-457, 01 Sep 1962
Cited by: 1 article | PMID: 14007033
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Some effects of verbal expression of hostillity.
DECHARMS R, WILKINS EJ
J Abnorm Soc Psychol, 66:462-470, 01 May 1963
Cited by: 2 articles | PMID: 14026295
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Air pollution bibliography.
WILKINS EJ
Air Water Pollut, 6:405-417, 01 Sep 1962
Cited by: 0 articles | PMID: 14000739
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1-25 of 25 results

Search life-sciences literature (45,103,477 articles, preprints and more)

Search results

Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years.

Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study.

Support for management actions to protect night sky quality: Insights from visitors to state and national park units in the U.S.

The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome.

Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.

Inherited variants in CHD3 demonstrate variable expressivity in Snijders Blok-Campeau syndrome

Social media reveal ecoregional variation in how weather influences visitor behavior in U.S. National Park Service units.

Uses and Limitations of Social Media to Inform Visitor Use Management in Parks and Protected Areas: A Systematic Review.

Attendance trends threaten future operations of America's state park systems.

Bringing forecasting into the future: Using Google to predict visitation in U.S. national parks.

Communicating information on nature-related topics: Preferred information channels and trust in sources.

Genetic Counseling in the Era of Genomics: What's all the Fuss about?

"It wasn't a disaster or anything": Parents' experiences of their child's uncertain chromosomal microarray result.

A DNA resequencing array for genes involved in Parkinson's disease.

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.

RUNX1 mutations are rare in chronic phase polycythaemia vera.

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips.

Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes.

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome.

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.

Two novel JAK2 exon 12 mutations in JAK2V617F-negative polycythaemia vera patients.

Multiplex ligation-dependent probe amplification (MLPA) genotyping assay for mouse models of down syndrome.

Authoritacanumand response to power cues.

Some effects of verbal expression of hostillity.

Air pollution bibliography.

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