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Development of Cleavage Line Patterns in the Skin of the Ovine Fetus

Okajimas Folia Anatomica Japonica, 1994/08/20, Vol.71(2-3), pp.143-159

1994

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Erupted upper teeth in a male sperm whale, Physeter macrocephalus

New Zealand journal of marine and freshwater research, 2001-06, Vol.35 (2), p.325-327

2001

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Macroinvertebrate production estimates in the Kanawha River, West Virginia

Hydrobiologia, 1994-04, Vol.281 (1), p.39-50

1994

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A comparison of three artificial substrate samplers: macroinvertebrate densities, taxa richness, and ease of use

Water environment research, 1994-05, Vol.66 (3), p.193-198

1994

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Differences in Macroinvertebrate Taxa Richness and Density between Samplers Located along the Shoreline and inside the Navigation Channel of the Kanawha River, West Virginia

Journal of freshwater ecology, 1993-03, Vol.8 (1), p.77-79

1993

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A neurophysiological study of nociceptive sensory mechanisms

Kirk, Edwin J

1974

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The dermatomes of the sheep

Journal of comparative neurology (1911), 1968-11, Vol.134 (3), p.353-369

Kirk, Edwin J.

1968

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Functional variation in dermatomes in the macaque monkey following dorsal root lesions

Journal of comparative neurology (1911), 1970-07, Vol.139 (3), p.307-320

1970

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Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders

Genetics in medicine, 2018-12, Vol.20 (12), p.1564-1574

2018

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Universal features of post-transcriptional gene regulation are critical for Plasmodium zygote development

PLoS pathogens, 2010-02, Vol.6 (2), p.e1000767-e1000767

2010

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Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System

JAMA : the journal of the American Medical Association, 2020-06, Vol.323 (24), p.2503

2020

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Sensitivity of leaf size and shape to climate: global patterns and paleoclimatic applications

The New phytologist, 2011-05, Vol.190 (3), p.724-739

2011

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Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission")

European journal of human genetics : EJHG, 2021-01, Vol.29 (1), p.79-87

2021

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A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures

Cell, 2018-02, Vol.172 (5), p.924-936.e11

2018

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Mutations in LYRM4, encoding iron-sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes

Human molecular genetics, 2013-11, Vol.22 (22), p.4460-4473

2013

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Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis

European journal of human genetics : EJHG, 2022-10, Vol.30 (10), p.1121-1131

2022

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The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy

Human mutation, 2020-08, Vol.41 (8), p.1425-1434

2020

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A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration

Cell reports (Cambridge), 2018-12, Vol.25 (10), p.2729-2741.e6

2018

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A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy

Cell reports (Cambridge), 2017-10, Vol.21 (4), p.926-933

2017

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Similarities and Differences in Left Ventricular Size and Function among Races and Nationalities: Results of the World Alliance Societies of Echocardiography Normal Values Study

Journal of the American Society of Echocardiography, 2019-11, Vol.32 (11), p.1396-1406.e2

2019

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Land cover, riparian zones and instream habitat influence stream fish assemblages in the eastern Amazon

Ecology of freshwater fish, 2019-04, Vol.28 (2), p.317-329

2019

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Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications

Journal of medical genetics, 2019-09, Vol.56 (9), p.629-638

2019

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Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort

Genetics in medicine, 2024-05, Vol.26 (5), p.101076, Article 101076

2024

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Examination of validity of identifying congenital heart disease from hospital discharge data without a gold standard: Using a data linkage approach

Paediatric and perinatal epidemiology, 2023-05, Vol.37 (4), p.303-312

2023

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Development of Cleavage Line Patterns in the Skin of the Ovine Fetus

Erupted upper teeth in a male sperm whale, Physeter macrocephalus

Macroinvertebrate production estimates in the Kanawha River, West Virginia

A comparison of three artificial substrate samplers: macroinvertebrate densities, taxa richness, and ease of use

Differences in Macroinvertebrate Taxa Richness and Density between Samplers Located along the Shoreline and inside the Navigation Channel of the Kanawha River, West Virginia

A neurophysiological study of nociceptive sensory mechanisms

The dermatomes of the sheep

Functional variation in dermatomes in the macaque monkey following dorsal root lesions

Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders

Universal features of post-transcriptional gene regulation are critical for Plasmodium zygote development

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System

Sensitivity of leaf size and shape to climate: global patterns and paleoclimatic applications

Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission")

A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures

Dominant missense mutations in ABCC9 cause Cantú syndrome

Mutations in LYRM4, encoding iron-sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes

Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis

The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy

A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration

A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy

Similarities and Differences in Left Ventricular Size and Function among Races and Nationalities: Results of the World Alliance Societies of Echocardiography Normal Values Study

Land cover, riparian zones and instream habitat influence stream fish assemblages in the eastern Amazon

Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications

Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort

Examination of validity of identifying congenital heart disease from hospital discharge data without a gold standard: Using a data linkage approach

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