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Peter Verveer Tishler M.D. (born July 18, 1937) is a researcher in human genetics and orphan diseases, educator, and clinician especially in the areas of genetic diseases, including polycystic kidney disease, chronic obstructive pulmonary disease, Fabry disease, and the porphyrias.
Early life and education
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Tishler was raised in New Jersey. His father, Max Tishler, was a senior research chemist and later president of Merck. Tishler attended public schools and Harvard College where he majored in Biochemical Sciences. He wrote his senior thesis on carboxypeptidase, in the lab of Dr. C.J. Fu at the Jimmy Fund, graduating cum laude in 1959.
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Tishler attended Yale School of Medicine. While at Yale, Tishler began working with the Thorndike Memorial Laboratory at Boston City Hospital. Dr. William B. Castle, discoverer of intrinsic factor, introduced him to Dr. Sidney H. Ingbar with whom Tishler began work on the metabolic actions of thyroid hormone. Dr. Maxwell Finland contributed to Tishler’s scientific and clinical work.[page needed] Tishler’s interest in genetics arose from his laboratory research in the study of thyroid function in patients with phenylketonuria.
During the Vietnam War, Tishler worked as a Public Health Service officer at the National Institutes of Health. In the following years, he continued his basic laboratory work, but also was concerned with genetics and medicine in the terms of population and epidemiology. He was also involved in familial studies of hypertension at one of the first community health centers in the U.S., East Boston Neighborhood Health Center.
- Linkage of serum leptin levels in families with sleep apnea. Int J Obes (Lond). 2005 Mar;29(3):260-7
- Whole genome scan for obstructive sleep apnea and obesity in African-American families. Am J Respir Crit Care Med. 2004 Jun 15; 169(12):1314-21. Epub 2004 Apr 7.
- Incidence of sleep-disordered breathing in an urban adult population: the relative importance of risk factors in the development of sleep-disordered breathing. JAMA. 2003 May 7;289(17):2230-7
- The effect of therapeutic drugs and other pharmacologic agents on activity of porphobilinogen deaminase, the enzyme that is deficient in intermittent acute porphyria. Life Sci. 1999;65(2):207-1
- Fetal alcohol effects in alcoholic veteran patients. Alcohol Clin Exp Res. 1998 Nov;22(8):1825-31
- A prospective study of plasma homocyst(e)ine and risk of myocardial infarction in US physicians. JAMA. 1992 Aug 19;268(7):877-81
- "The care of the patient": a living testimony to Francis Weld Peabody. Pharos Alpha Omega Alpha Honor Med Soc. 1992 Summer;55(3):32-6
- Thoughts as I watched the Peabody Building fall, March 31, 1990. N Engl J Med. 1990 Oct 11;323(15):1074
- Healthy female carriers of a gene for the Alport syndrome: importance for genetic counseling. Clin Genet. 1979 Oct;16(4):291-4
- A family with coexistent von Recklinghausen's neurofibromatosis and von Hippel-Lindau's disease. Diseases possibly derived from a common gene. Neurology. 1975 Sep;25(9):840-4.
- Phenylketonuria: therapeutic problems. Br Med J. 1969 Feb 22;1(5642):510
- Effect of thyroxine administered in vitro and in vivo on the succinoxidase and malic dehydrogenase reactions of frog myocardium.Endocrinology. 1963 May;72:673-6
- Finland, Maxwell and Castle, William B., Eds. (1983) The Harvard Medical Unit at Boston City Hospital, Volume II. University of Virginia Press (for the Francis A. Countway Library of Medicine).