PubRank

M Malone

Author PubWeight™ 109.54‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Infection and sudden unexpected death in infancy: a systematic retrospective case review. Lancet 2008 3.44
2 Crystal structure of the human prion protein reveals a mechanism for oligomerization. Nat Struct Biol 2001 2.19
3 Hypocalcaemia and vitamin D deficiency: an important, but preventable, cause of life-threatening infant heart failure. Heart 2007 2.04
4 Challenges to implementation of the new Coroners' (Amendment) Rules 2005: experience from a tertiary paediatric pathology centre. Med Sci Law 2007 1.92
5 The role of post-mortem investigations in determining the cause of sudden unexpected death in infancy. Arch Dis Child 2008 1.77
6 Capillary apposition and density in the diagnosis of alveolar capillary dysplasia. Histopathology 2008 1.62
7 Ingested interferon alpha suppresses type I diabetes in non-obese diabetic mice. Diabetologia 1998 1.59
8 Serotonin syndrome induced by fluvoxamine and mirtazapine. Ann Pharmacother 2001 1.43
9 Myogenin and MyoD1 expression in paediatric rhabdomyosarcomas. J Clin Pathol 2003 1.42
10 Functioning adrenocortical neoplasms in children. BJU Int 2002 1.39
11 Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder. Mol Psychiatry 2000 1.31
12 Blood film examination for vacuolated lymphocytes in the diagnosis of metabolic disorders; retrospective experience of more than 2,500 cases from a single centre. J Clin Pathol 2005 1.27
13 The biophysics of differential growth. Environ Exp Bot 1989 1.27
14 Association between Clostridium difficile and enterocolitis in Hirschsprung's disease. Lancet 1982 1.26
15 Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder. Genes Brain Behav 2006 1.24
16 Circulating melanoma cells and survival in metastatic melanoma. Int J Oncol 2011 1.21
17 Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder. Mol Psychiatry 2004 1.16
18 Specific autoantibodies to gut epithelium in two infants with severe protracted diarrhoea. J Pediatr Gastroenterol Nutr 1985 1.15
19 Direct measurement of sodium and potassium in the transpiration stream of salt-excluding and non-excluding varieties of wheat. J Exp Bot 2001 1.12
20 Preoperative binge eating status and gastric bypass surgery: a long-term outcome study. Obes Surg 2008 1.11
21 The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder. Mol Psychiatry 2005 1.10
22 Chromium picolinate toxicity. Ann Pharmacother 1998 1.08
23 Glutathione in health and disease: pharmacotherapeutic issues. Ann Pharmacother 1995 1.08
24 Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia). J Med Genet 1998 1.07
25 Congenital alveolar rhabdomyosarcoma: clinical and molecular distinction from alveolar rhabdomyosarcoma in older children. Cancer 2001 1.04
26 Diversion procto-colitis: response to treatment with short-chain fatty acids. J Pediatr Surg 2001 1.02
27 Congenital alveolar capillary dysplasia and associated gastrointestinal anomalies. Fetal Pediatr Pathol 2006 1.02
28 A flow cytometric study of Langerhans cell histiocytosis. Br J Dermatol 1989 1.01
29 Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder. Biol Psychiatry 2001 1.01
30 The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder. Mol Psychiatry 2003 1.00
31 Pathology of astrovirus associated diarrhoea in a paediatric bone marrow transplant recipient. J Clin Pathol 2004 1.00
32 Histopathological features of chronic granulomatous disease (CGD) in childhood. Histopathology 2005 1.00
33 Melanotic neuroectodermal tumor of infancy: clinical, radiological, and pathological features. Fetal Pediatr Pathol 2006 0.99
34 Isolated EBV lymphoproliferative disease in a child with Wiskott-Aldrich syndrome manifesting as cutaneous lymphomatoid granulomatosis and responsive to anti-CD20 immunotherapy. J Clin Pathol 2003 0.98
35 Technique and use of transbronchial biopsy in children and adolescents. Pediatr Pulmonol 1992 0.97
36 Langerhans cell histiocytosis: the case for conservative treatment. Arch Dis Child 1990 0.97
37 Clinicopathological features of paediatric deaths due to myocarditis: an autopsy series. Arch Dis Child 2008 0.95
38 Cytogenetic analysis of primitive neuroectodermal tumors. Absence of the t(11;22) in two of three cases and a review of the literature. Cancer Genet Cytogenet 1991 0.95
39 Rhabdomyosarcoma in children: a histological and immunohistochemical study of 59 cases. J Pathol 1989 0.93
40 Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region. Mol Psychiatry 2004 0.93
41 Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder. Am J Med Genet 1999 0.92
42 Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder. Mol Psychiatry 2005 0.91
43 Spontaneous remission of congenital leukemia: a case for conservative treatment. J Pediatr Hematol Oncol 2000 0.91
44 BCL-2 expression by leukaemic blasts in a SCID mouse model of biphenotypic leukaemia associated with the t(4;11)(q21;q23) translocation. Br J Haematol 1995 0.91
45 Liver failure associated with mitochondrial DNA depletion. J Hepatol 1998 0.90
46 Open lung biopsy in neonatal and paediatric patients referred for extracorporeal membrane oxygenation (ECMO). Thorax 2004 0.90
47 Pulmonary involvement by Niemann-Pick disease. A report of six cases. Histopathology 2006 0.90
48 5'-untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder. Am J Med Genet 2001 0.89
49 Early treatment of juvenile xanthogranuloma of the iris with subconjunctival steroids. Br J Ophthalmol 1993 0.89
50 Improved outcome for children with hepatoblastoma. Br J Surg 1995 0.89
51 Colon involvement in Langerhans' cell histiocytosis. J Pediatr Gastroenterol Nutr 1999 0.88
52 Association study of the nicotinic acetylcholine receptor alpha4 subunit gene, CHRNA4, in attention-deficit hyperactivity disorder. Genes Brain Behav 2007 0.88
53 Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder. Am J Med Genet 2000 0.87
54 Pulmonary alveolar microlithiasis in childhood: diagnosis by transbronchial biopsy. Pediatr Pulmonol 1996 0.87
55 Beta blocker use in the treatment of community hospital patients discharged after myocardial infarction. J Gen Intern Med 1994 0.87
56 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency; effect of chenodeoxycholic acid therapy on liver histology. J Inherit Metab Dis 1992 0.87
57 Hepatoblastoma and polyposis coli (familial adenomatous polyposis) Med Pediatr Oncol 1989 0.86
58 Diagnosis of neuronal ceroid lipofuscinosis (Batten disease) by electron microscopy in peripheral blood specimens. Ultrastruct Pathol 2006 0.86
59 Histopathological reporting of paediatric cutaneous vascular anomalies in relation to proposed multidisciplinary classification system. J Clin Pathol 2006 0.86
60 Linkage of the dopamine D4 receptor gene and attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2000 0.86
61 Teacher-identified oral language difficulties among boys with attention problems. J Dev Behav Pediatr 1994 0.85
62 Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder (ADHD). Mol Psychiatry 2000 0.85
63 Epstein-Barr virus-associated lymphoproliferative disorder presenting as apparently isolated gastrointestinal lesions in childhood. Pediatr Dev Pathol 2005 0.84
64 Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder. Am J Med Genet 2000 0.84
65 LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome. Br J Dermatol 2004 0.84
66 Juvenile xanthogranuloma as a sequel to Langerhans cell histiocytosis: a report of three cases. Clin Exp Dermatol 2001 0.84
67 Histological examination in sudden unexpected death in infancy: evidence base for histological sampling. J Clin Pathol 2011 0.84
68 Tibia vara due to focal fibrocartilaginous dysplasia. The natural history. J Bone Joint Surg Br 1988 0.83
69 Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre. J Clin Pathol 2005 0.83
70 Comparison of programs for preventing drug-nutrient interactions in hospitalized patients. Am J Health Syst Pharm 1997 0.83
71 Intracardiac epithelial cyst associated with esophageal atresia. Pediatr Pathol Lab Med 1997 0.82
72 Brain damage after cardiopulmonary by-pass: correlations between neurophysiological and neuropathological findings. J Neurol Neurosurg Psychiatry 1981 0.82
73 Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder. Am J Med Genet 2001 0.82
74 Beneficial effects of pharmacotherapy on weight loss, depressive symptoms, and eating patterns in obese binge eaters and non-binge eaters. Obes Res 1999 0.81
75 Desmin expression in rhabdomyosarcoma: influence of the desmin clone and immunohistochemical method. J Clin Pathol 1995 0.81
76 Maxillary myxoma: a rare midfacial mass in a child. Int J Pediatr Otorhinolaryngol 2000 0.81
77 Ultrastructural features of gaucher disease treated with enzyme replacement therapy presenting as mesenteric mass lesions. Fetal Pediatr Pathol 2007 0.81
78 Histopathological features of testicular regression syndrome: relation to patient age and implications for management. Fetal Pediatr Pathol 2006 0.81
79 Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor. Mol Psychiatry 2000 0.81
80 Cost and outcome analysis of home parenteral and enteral nutrition. JPEN J Parenter Enteral Nutr 1998 0.80
81 Childhood soft tissue chondroma: a case report. Pediatr Pathol Lab Med 1996 0.80
82 Virological investigations in sudden unexpected deaths in infancy (SUDI). Forensic Sci Med Pathol 2010 0.79
83 Attention-deficit hyperactivity disorder and the adrenergic receptors alpha 1C and alpha 2C. Mol Psychiatry 2001 0.79
84 Clinical outcome of geriatric patients in the United States receiving home parenteral and enteral nutrition. Am J Clin Nutr 1997 0.79
85 Inherited ichthyoses: a review of the histology of the skin. Pediatr Pathol Lab Med 1997 0.79
86 Astrocytoma as a second malignancy in patients with acute lymphoblastic leukemia. Cancer 1986 0.79
87 Tandem mass spectrometry findings at autopsy for detection of metabolic disease in infant deaths: postmortem changes and confounding factors. J Clin Pathol 2011 0.79
88 Outcomes of pharmacological and surgical treatment for obesity. Pharmacoeconomics 1998 0.79
89 Chemotherapy effects on hepatoblastoma. A histological study. Am J Surg Pathol 1993 0.79
90 Linkage study of the alpha2A adrenergic receptor in attention-deficit hyperactivity disorder families. Am J Med Genet 2001 0.78
91 Omenn's syndrome: differential diagnosis in infants with erythroderma and immunodeficiency. Pediatr Dev Pathol 2001 0.78
92 Eosinophilic granuloma of lymph nodes associated with metastatic papillary carcinoma of the thyroid. Histopathology 1992 0.78
93 Parent-child transmission of infantile cholestasis with lymphoedema (Aagenaes syndrome). J Med Genet 1997 0.78
94 Update on the pharmacotherapy of obesity. Ann Pharmacother 1998 0.78
95 Deletion of part of the short arm of chromosome 17 in a congenital fibrosarcoma. Cancer Genet Cytogenet 1990 0.78
96 Osteosarcoma--presumed lymph node metastases in two cases. Skeletal Radiol 1989 0.78
97 Histopathological features of open lung biopsies in children treated with extracorporeal membrane oxygenation (ECMO). Early Hum Dev 2004 0.78
98 Isolated unilateral tuberous sclerosis-associated renal cystic disease in a neonate. Fetal Pediatr Pathol 2006 0.78
99 Gains of chromosome 8 in pleuropulmonary blastomas of childhood. Pediatr Dev Pathol 2002 0.77
100 Association of the KCNJ5 gene with Tourette Syndrome and Attention-Deficit/Hyperactivity Disorder. Genes Brain Behav 2014 0.77
101 Focal or diffuse lesions in persistent hyperinsulinemic hypoglycemia of infancy: concerns about interpretation of intraoperative frozen sections. Pediatr Dev Pathol 2001 0.77
102 Staphylococcal toxins in sudden unexpected death in infancy: experience from a single specialist centre. Forensic Sci Med Pathol 2010 0.77
103 Michelin-tire baby syndrome resulting from diffuse smooth muscle hamartoma. Pediatr Dermatol 1989 0.77
104 Studies of the in vitro effect of methylmercury chloride on rat brain neurotransmitter enzymes. J Appl Toxicol 1987 0.77
105 No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder. Mol Psychiatry 2007 0.77
106 Current status of home parenteral nutrition in the United States. Transplant Proc 1996 0.77
107 Assessment of drug-related problems in clinical nutrition patients. JPEN J Parenter Enteral Nutr 1999 0.76
108 Adoptive transfer from interferon-alpha-fed mice is associated with inhibition of active experimental autoimmune encephalomyelitis by decreasing recipient tumor necrosis factor-alpha secretion. J Immunother 2000 0.76
109 Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region. Genes Brain Behav 2008 0.76
110 Pathology teach and tell: pediatric gastrointestinal stromal tumor. Pediatr Pathol Mol Med 2003 0.75
111 Drug-food interactions in hospitalised patients. Methods of prevention. Drug Saf 1998 0.75
112 Association between azathioprine therapy and lymphoma in rheumatoid disease. J R Soc Med 1987 0.75
113 Pellagra with colitis due to a defect in tryptophan metabolism. Eur J Pediatr 1991 0.75
114 Hospice care. Am J Nurs 1998 0.75
115 Changing patterns of infant death over the last 100 years: autopsy experience from a specialist children's hospital. J R Soc Med 2012 0.75
116 "Liver mass in a 4 year old child:....." by Applebaum et al. Med Pediatr Oncol 1990 0.75
117 The diagnosis of Hirschsprung's disease. Hum Pathol 1993 0.75
118 School-community relations. Health fair for the campus community. Sch Health Rev 1974 0.75
119 Aspirin administration for cardiac-related acute chest pain/angina: increased use in Medicare patients. South Med J 1999 0.75
120 Chitin as a causative mechanism for inflammatory disease. J Theor Biol 1975 0.75
121 Synthesis and preliminary screening of N-ethyltryptamine derivatives related to reserpine and lysergic acid. J Pharm Sci 1971 0.75
122 Acquisition and generalization of social skills by high school students with mild mental retardation. Ment Retard 1995 0.75
123 Improvement of coronary artery disease in a patient with hyperhomocysteinemia: report of a case. Nutrition 1998 0.75
124 Massive cardiac chondroma presenting with heart failure and superior vena cava obstruction in a teenage boy. Fetal Pediatr Pathol 2005 0.75
125 Lipoatrophic panniculitis and chromosome 10 abnormality. Br J Dermatol 2000 0.75
126 Adrenal cortical tumours in children. Eur J Radiol 1994 0.75
127 Sectional morphology of the first metatarsophalangeal joint. J Foot Ankle Surg 1994 0.75
128 Operations research in outpatient services. World Hosp 1978 0.75
129 Meet the President: William J. Kinnard Jr. Am J Pharm Educ 1976 0.75
130 Primary hepatic malignant tumor with rhabdoid features. A histological, immunocytochemical, and electron microscopic study of four cases and a review of the literature. Am J Surg Pathol 1996 0.75
131 Unit in review. John Hunter Teaching Hospital. Confed Aust Crit Care Nurses J 1991 0.75
132 Extensive enteric leiomyolysis due to cytomegalovirus enterocolitis in vertically acquired human immunodeficiency virus infection in infants. Pediatr Dev Pathol 2000 0.75
133 Use of supplemental oxygen during bystander-initiated CPR. Ann Emerg Med 1994 0.75
134 Primary thoracic myxoid variant of extrarenal rhabdoid tumor in childhood. Fetal Pediatr Pathol 2006 0.75
135 Renal transplant patients' knowledge concerning cyclosporine treatment. Clin Nephrol 1991 0.75
136 Lethal congenital erythroderma: a newly recognised genetic disorder. Clin Genet 1992 0.75
137 Risk of germ cell malignancy in children with XY intersex versus isolated cryptorchidism by immunohistochemistry. Fetal Pediatr Pathol 2006 0.75
138 The U.S. Marine Corps: a consequence response partner. Emerg Med Serv 2000 0.75
139 Predictive accuracy of the TRISS survival statistic is improved by a modification that includes admission pH. Arch Surg 1995 0.75
140 Postpartum testing for antecedent gestational diabetes. Am J Obstet Gynecol 1988 0.75
141 4-S neuroblastoma on high field MR. Pediatr Radiol 1989 0.75
142 Proliferative myositis in a child. A case report. J Bone Joint Surg Am 1995 0.75
143 Cefazolin use in clinically severe obese patients undergoing gastric restrictive surgery. Ann Pharmacother 1995 0.75
144 Synthesis of ordinary and -hydroxy fatty acids by heart mitochondria. Arch Biochem Biophys 1972 0.75
145 Electron microscopy of chorionic villus samples for prenatal diagnosis of lysosomal storage disorders. Ultrastruct Pathol 2007 0.75
146 Facial features of widespread neuroblastoma: a case report. Int J Paediatr Dent 2001 0.75
147 Comparison between continuous and intermittent infusion regimens of cimetidine in ulcer patients. Clin Pharmacol Ther 1989 0.75
148 An investigation into information provided for patients on home parenteral nutrition. J Clin Pharm Ther 1988 0.75
149 Cardiac metabolism of beta-hydroxy fatty acids. Recent Adv Stud Cardiac Struct Metab 1973 0.75
150 Skeletal-muscle haemangioma presenting as an abdominal mass. Br J Radiol 1986 0.75
151 A frequent attender. Practitioner 1995 0.75
152 Waxy keratoses of childhood. Clin Exp Dermatol 1994 0.75